• Title/Summary/Keyword: concentration dependence

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Rheology and morphology of concentrated immiscible polymer blends

  • Mewis, Jan;Jansseune, Thomas;Moldenaers, Paula
    • Korea-Australia Rheology Journal
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    • v.13 no.4
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    • pp.189-196
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    • 2001
  • The phase morphology is an important factor in the rheology of immiscible polymer blends. Through its size and shape, the interface between the two phases determines how the components and the interface itself will contribute to the global stresses. Rheological measurements have been used successfully in the past to probe the morphological changes in model blends, particularly for dilute systems. For more concentrated blends only a limited amount of systematic rheological data is available. Here, viscosities and first normal stress differences are presented for a system with nearly Newtonian components, the whole concentration range is covered. The constituent polymers are PDMS and PIB, their viscosity ratio can be changed by varying the temperature. The data reported here have been obtained at 287 K where the viscosities of the two components are identical. By means of relaxation experiments the measured stresses are decomposed into component and interfacial contributions. The concentration dependence is quite different for the two types of contribution. Except for the component contributions to the shear stresses there is no clear indication of the phase inversion. Plotting either the interfacial shear or normal stresses as a function of composition produces in some cases two maxima. The relaxation times of these stresses display a similar concentration dependence. Although the components have the same viscosity, the stress-component curves are not symmetrical with respect to the 50/50 blend. A slight elasticity of one of the components seems to be the cause of this effect. The data for the more concentrated blends at higher shear rates are associated with a fibrillar morphology.

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Functions and Power Laws of Critical Micelle Concentration with Respect to Temperature (임계 마이셀 농도의 온도 함수와 지수 법칙)

  • Lim, Kyung-Hee;Kim, Hong-Un;Kang, Kye-Hong
    • Applied Chemistry for Engineering
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    • v.17 no.5
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    • pp.443-450
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    • 2006
  • Micelles have been used in many applications. In these applications it is of prime importance to know how the critical micelle concentration (CMC), above which the micelles are formed, depends on temperature. Up to date polynomial functions of temperature have been used to describe temperature dependence of CMC. In this article it is shown that such polynomials are inadequate tools to express thermal behavior of CMC. Hence, new equations of CMC(T) have been derived on the basis of rigorous thermodynamic equations and experimental observations on CMCs. The new equations fit CMC data excellently, and further they lead to a power law for the CMC. The exponent of the power-law expression is 2 irrespective of surfactant systems, which points to the generality of newly found equations.

Surface Morphology and Quantum Size Effect of ZnS Thin Film Grown by Solution Growth Technique (용액성장된 ZnS 박막의 표면형상 및 양자사이즈효과)

  • Lee, Jong-Won;Lee, Sang-Uk;Jo, Seong-Ryong;Kim, Seon-Tae;Park, In-Yong
    • Korean Journal of Materials Research
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    • v.12 no.1
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    • pp.36-43
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    • 2002
  • In this study, the nanosized ZnS thin films that can be used for fabrication of blue light-emitting diodes, electro-optic modulators, and n-window layers of solar cells were grown by the solution growth technique (SGT), and their surface morphology and film thickness and grain size dependence on the growth conditions were examined. Based on these results, the quantum size effects of ZnS were systematically investigated. Governing factors related to the growth condition were the concentration of precursor solution, growth temperature, concentration of aq. ammonia, and growth duration. X-ray diffraction patterns showed that the ZnS thin film obtained in this study had the cubic structure ($\beta$-ZnS). With decreasing growth temperature and decreasing concentration of precursor solution, the surface morphology of film was found to be improved. Also, the film thickness depends largely on the ammonia concentration. In particular, this is the first time that the surface morphology dependence of ZnS film grown by SGT on the ammonia concentration is reported. The energy band gaps of samples were determined from the optical transmittance values, and were shown to vary from 3.69 eV to 3.91 eV. These values were substantially higher than 3.65 eV of bulk ZnS. It was also shown that the quantum size effect of SGT grown ZnS is larger than that of the ZnS films grown by most other growth techniques.

Thermodynamic Parameters for Micelle Formation of Dodecylpyridinium Chloride (Dodecylpyridinium Chloride의 micelle 形成의 熱力學變數)

  • Han, Man-Un
    • Journal of the Korean Chemical Society
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    • v.10 no.2
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    • pp.103-108
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    • 1966
  • The effect of temperature on the critical micelle concentration of dodecylpyridinium chloride has been determined by electrical conductance method over the range from $5^{\circ}C\;to\;50^{\circ}C$. The values of the change in heat content, ${\Delta}H_m$, and the other thermodynamic parameters have been estimated using the equation of temperature dependence on the critical micelle concentration for the same temperature range. The significance of these thermodynamic quantities and their relations to the various current theories of micelle forming processes were discussed.

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실크 피브로인의 겔화

  • Kim, Dong-U;Ha, Seong-Jin;Im, Geon-Bin;Heo, Won
    • 한국생물공학회:학술대회논문집
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    • 2001.11a
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    • pp.798-799
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    • 2001
  • The intermolecular hydrogen bond between silk fibroin in aqueous solution facilitates gelation of silk fibroin. The dependence of gelation by the concentration of silk fibroin, pH and temperature was investigated. The gelation time of silk fibroin is decreased with increasing the concentration of glycerol and temperature within a limited range. The pH optimum for gelation found out to be 9. Hydrophobic additives were investigated to reduce gelation time.

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Optimum Substrate Temperature for Hydrogenated Amorphous Silicon $n^+-p-p^+$ Cells (수소화된 비정질 실리콘 $n^+-p-p^+$ 태양전지에서 최적기판온도의 결정)

  • Lee, Yi-Sang;Jang, Jin
    • Proceedings of the KIEE Conference
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    • 1987.07a
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    • pp.509-512
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    • 1987
  • We report that the optimum substrate temperature to fabricate a-Si:H $n^+-p-p^+$ cell decreases with increasing the boron concentration in the Player. The results can be explained as the dependence of substrate temperature for the relaxation of silicon atoms and the bonded hydrogen concentration in the player.

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Electro-Magnetic Properties of Mn-Zn Ferrite Single Crystal with Small Variation of $Fe_2O_3$ Concentration ($Fe_2O_3$ 미량 변화에 따른 Mn-Zn 페라이트 단결정의 전자기적 특성)

  • 제해준;변순천;홍국선;장성도
    • Journal of the Korean Ceramic Society
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    • v.30 no.10
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    • pp.791-796
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    • 1993
  • The electro-magnetic properties of the Mn-Zn ferrite single crystal with small variation of Fe2O3 concentration at the high permeability composition, 53mol% Fe2O3-28.5mol% MnO-18.5mol% ZnO, have been studied for the VCR magnetic head application. With the increase of the Fe2O3 concentration, the Fe2+ concentration increased, the specific resistivity decreased, the secondary maximum permeability shifted to the lower temperature, and the initial permeability decreased. It was concluded that the small variation of $\pm$0.5mol% Fe2O3 concentration greatly affected the electro-magnetic properties of Mn-Zn ferrite single crystals. At the composition of 53mol% Fe2O3, the initial permeability was comparatively high (650 at 5MHz) and its temperature dependence was small.

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CONCENTRATION DEPENDENCES OF GROUND-STATE AND EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER OF PIROXICAM IN METHANOL

  • Cho, Dae-Won;Kang, Seong-Gwan;Kim, Yong-Hee;Yoon, Min-Joong;Kim, Dong-Ho
    • Journal of Photoscience
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    • v.1 no.1
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    • pp.15-23
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    • 1994
  • The absorption and fluorescence spectral properties of piroxicam (PRX) in the hydrogenbonding solvents show the most sensitive dependence on the concentration ranging from 8 x 10$^{_5}$ to 2 x10$^{_5}$ M. These are attributed to both the solvent-mediated ground-state intermolecular proton transfer (GSIerPT) leading to formation of the ground state anion and the excited-state intmmolecular proton transfer (ESIraPT). The concentration dependences of the time-resolved emission kinetics at both room temperature and 77 K have also been investigated. It is shown that in the excited state, the ESIraPT of PRX is the dominant process to form a keto tautomer at the high concentration, whereas at the low concentration the excited-state conformational change of the anion is an additional process leading to formation of a zwitterion. The ESI~PT of PRX in the hydrogenbonding solvent is coupled with the ultrafast excited-state solvent reorganization.

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