• Title/Summary/Keyword: miscibility.

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An Experimental Study on Miscibility and Vapor Pressure of R-744/Oil Mixtures (R-744/오일 혼합물의 상용성 및 증기압에 관한 실험적 연구)

  • 최희성;강병하;박경근;김석현
    • Korean Journal of Air-Conditioning and Refrigeration Engineering
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    • v.16 no.2
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    • pp.150-157
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    • 2004
  • Carbon dioxide ($CO_2$, R-744) has become a very popular issue in application to refrigeration and air conditioning systems as a natural refrigerant. An experimental study has been carried out to investigate miscibility and the vapor pressure of refrigerant R-744 in the presence of lubricant oil. This is of particular interest in the selection of the lubricant oil for the compressor of a refrigeration system or an air conditioning system using the refrigerant R-744. The experimental set-up consists of the equilibrium cell, measuring devices, the vacuum pump, the constant temperature bath and relevant connecting pipes made of stainless steel. Five lubricant oils, such as mineral oil (Naphthenic), AB (Alkyl Benzene) oil, PAO (Poly Alpha Olefin) oil, PAG (Poly Alkylene Glycol) oil and POE (Polyol Ester) oil are considered in the present study. Test runs were conducted with the oil concentration range from 5 to 50 wt%, and the temperature range from -10 to 1$0^{\circ}C$ with 2$^{\circ}C$ intervals. The miscibility results are visualized and correlated with the vapor pressure for the individual test components.

Reactivity Considerations with Miscibility of Process Gases in Semiconductor industry (반도체 산업 공정가스의 혼화성에 따른 반응성 고찰)

  • Lee, Keun Won
    • Journal of the Korean Institute of Gas
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    • v.20 no.4
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    • pp.15-24
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    • 2016
  • In the semiconductor industry, the risk of chemical accidents due to miscibility between the many types of chemicals and leakage of toxic chemicals has increased. In order to evaluate the reactivity with miscibility of chemicals, experimental method is the most reliable, but there is a time and cost limitations to be evaluated through experiment all the chemicals. In the study, the reactivity of process gases in the semiconductor industry was considered by the CRW (Chemical Reactivity Worksheets) 3.0 program developed by US NOAA (National Oceanic and Atmospheric Administration) and EPA. The reactivity informations with the miscibility of process gases for semiconductor industry provided, and also a KOSHA guide for the storage/separation of gas cylinders in dispensing cabinets in the semiconductor industry was proposed.

Measurement of solubility and miscibility of R-410A/POE oil mixture (R-410A/POE 오일 혼합물의 용해도 및 상용성 측정)

  • 송준석;김창년;박영무
    • Korean Journal of Air-Conditioning and Refrigeration Engineering
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    • v.12 no.2
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    • pp.209-217
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    • 2000
  • The solubility and miscibility measurement apparatus was developed and used to obtain data for refrigerant/oil mixture. The solubility and miscibility data for R-410A/68 ISO VG polyol ester (POE) oil mixture are obtained over the temperature range from -20 to $60^{circ}C\;with\;10^{\circ}C$ intervals and the oil concentration range from 0 to 90 wt%. Using the experimental data, an empirical model was developed to predict the solubility relations for R-410A/POE oil mixture at equilibrium. In the R-410A/Solest 68 oil mixture, the average root-mean-square deviation between measured data and calculated results from the empirical model is 3.4% and in the R-4104/EMKARATE RL 68H oil mixture, that is 2.86%. For R-410A/68 ISO VG POE oil mixture immiscibility was usually observed at the low oil concentrations(5~30 wt%) over the all experimental temperature range($-20~60^{circ}C$) and at the high oil concentrations(50~90 wt%) over the low experimental temperature range($-2O~0^{circ}C$).

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Synthesis and Applications of Reactive Polymer Modifiers for Asphalt(1) (아스팔트용 반응성 고분자 개질제 합성 및 적용(1))

  • Hwang, Ki-Seob;Ahn, Won-Sool;Suh, Soong-Hyuck;Ha, Ki-Ryong
    • Polymer(Korea)
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    • v.31 no.1
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    • pp.68-73
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    • 2007
  • This study is on the synthesis of reactive polymer modifiers by emulsion polymerization to improve properties of asphalt for paving. Styrene, methyl methacrylate (MMA), isoprene and glycidyl methacrylate (GMA) which has epoxy ring to react with carboxyl group of asphaltene were used to synthesize polymer modifiers. Modifiers with various composition were tested miscibility with asphalt. Modifiers which showed good miscibility with asphalt were investigated by DSC for $T_g$. Existence of epoxy rings and their reaction with asphaltene wore investigated by FTIR. Molecular structures of synthesized modifiers were confirmed by $^1H-NMR$. The synthesized modifiers which showed good miscibility had their $Tg's$ in the range of $37.5{\sim}56.5^{\circ}C$ and had isoprene contents of 30 wt%. They showed good miscibility in the 1 and 2 wt% concentrations, but not in the 3 wt% concentration.

Properties and Biodegradability of Polylactide for Paper Coating Application - $Poly(_{L} -lactide)\;and\;Poly(_{D}-lactide)$ Blend -

  • Lim Hyun A;Kang Jin Ha
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.36 no.5 s.108
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    • pp.53-61
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    • 2004
  • [ $Poly(_{D}-ldactide)\;(_{D}-PLA)$ ] was synthesized to have low molecular weight for miscible blends with a high molecular $poly(_{L}-lactide)\;(_{L} -PLA)$. The blends were prepared by dissolving the two components of $_{L}-PLA\;and\;_{D}-PLA\;(w/w)$ in chloroform (l00/0, 90/10, 70/30, 50/50, 30/70, 0/100). The miscibility of these miscible blends was characterized by gel-permeation chromatography (GPC), differential scanning calorimetry (DSC), and the selective degradability by enzymes (proteinase K, subtilisin and $\alpha$-chymotrypsin). The coating efficiency of PLA blends onto paper was determined and the degrading activity cellulases by on these blends. The miscibility, coating efficiency and enzymatic degradability of these blends were decreased according to increasing of $_{D}-PLA$ blending part. Such results were attributed to the extent of coating application of PLA, with better miscibility (compatibility), coating efficiency and degradability due to a higher $_{L}-PLA$ content.

Solid-state NMR Studies of Miscibility and Morphology in Blends of Bisphenol-A type Polycarbonate and Poly (ester-ether) Elastomer

  • Kim, Yongae
    • Journal of the Korean Magnetic Resonance Society
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    • v.5 no.1
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    • pp.19-28
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    • 2001
  • Miscibility and morphology in blends of bisphenol-A type polycarbonate and poly (ester-ether) elastomer with different compositions are studied by solid-state NMR spectroscopy. $^{13}$ C Solid-state NMR of CP/MAS/TOSS/DD, CP/MAS/DD, inversion recovery CP/MAS/DD, and 2D rotor driven spin diffusion techniques are used to identify the miscibility, morphology, and transesterification in blends. The blends of PC /BT elastomer with 15% to 42% of soft segment seem to be single phase miscible mixing and those of PC/PBT and PC/PBT elastomer with 62% of soft segment are cocontinuous two phase immiscible mixing. No significant transesterification reactions are observed in blends with different compositions.

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Effect of Acrylonitrile Content on the Glass Transition Temperature and Melt Index of PVC/SAN Blends

  • Liu Wang;Kim Hwan-Chul;Pak Pyong-Ki;Kim Jong-Chun
    • Fibers and Polymers
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    • v.7 no.1
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    • pp.36-41
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    • 2006
  • PVC and SAN are often mixed to compensate for the disadvantages of each polymer. Miscibility and thermal stability of PVC/SAN blend were investigated in this study by blending SAN polymer having 20, 24, 28, 32 % of acrylonitrile contents. Two polymers were mixed using a melt blending method with a single screw extruder. DSC thermogram was used to evaluate miscibility of the two polymers. SAN having 24 % of acrylonitrile showed the best miscibility with PVC. In order to evaluate degradation behavior, blended polymer was heat treated in DSC furnace and glass transition temperature was measured consecutively. Glass transition temperature increased continuously with annealing time due to degradation and cross-linking of polymer chains. Melt index of blended polymer was always higher than that of PVC.

Miscibility of Polysulfone/Poly(1-vinylpyrrolidone-co-styrene) Blends and Their Application to the Ultrafiltration Membrane

  • Kim, Joo-Heun;Yoo, Jung-Eun;Kim, Chang-Keun
    • Macromolecular Research
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    • v.10 no.4
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    • pp.209-214
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    • 2002
  • Miscibility of polysulfone (PSf) with various hydrophilic copolymers was explored. Among these blends, PSf gives homogeneous mixtures with poly(1-vinylpyrrolidone-co-styrene) copolymers [P(VP-S)] when these copolymers contained VP from 68 to 88 wt%. Microporous membranes for the ultrafiltration process were prepared from PSf blends with P(VP-S) copolymers. The membranes prepared from the PSf/(VP-S) blends exhibited higher water flux than the membranes prepared from PSf irrespective of the VP content. The solute rejection examined with the membranes fabricated from the miscible blends was similar to that of PSf membrane. However, the solute rejection examined with the membranes fabricated from the immiscible blends was lower than that of PSf membranes.

Miscibility in Binary Blends of Poly(vinyl phenol) and Poly(n-alkylene 2,6-naphthalates)

  • Lee, Joon-Youl;Han, Ji-Young
    • Macromolecular Research
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    • v.12 no.1
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    • pp.94-99
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    • 2004
  • We have performed Fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC) studies on blends of poly(vinyl phenol) (PVPh) with poly(n-alkylene 2,6-naphthalates) containing alkylene units of different lengths. The results indicate that each poly(ethylene 2,6-naphthalate) (PEN) and poly(trimethylene 2,6-naphthalate) (PTN) blend with PVPh is immiscible or partially miscible, but blends of poly(butylene 2,6-naphthalate) (PBN) with PVPh are miscible over the whole range of compositions in the amorphous state. FTIR spectroscopic analysis confirmed that significant degree of intermolecular hydrogen bonding occurs between the PBN ester carbonyl groups and the PVPh hydroxyl groups. The large difference in the degree of mixing in these blend systems is described in terms of the effect that chain mobility has on the accessibility of the ester carbonyl functional groups toward the hydroxyl groups of PVPh, which in turn impacts the miscibility of these blends.

Miscibility and Phase Separation Behavior of P(VDF-co-HFP) and Poly(vinyl methyl ketone) Blends (P(VDF-co-HFP)와 poly(vinyl methyl ketone) 블렌드물의 혼화성 및 상분리 거동)

  • 김영호;홍성돈;김갑진
    • Proceedings of the Korean Fiber Society Conference
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    • 2003.04a
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    • pp.319-320
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    • 2003
  • 압전성과 초전성을 나타내는 고분자인 poly(vinylidene fluoride)(PVDF)는 poly(methyl methacrylate), poly(vinyl acetate), 및 Poly(vinyl methyl ketone)(PVMK) 등과 블렌딩하면 혼화성(miscibility)이 있다. 이들 블렌드물들을 용융온도 이상으로 승온시키면 낮은 온도에서는 균일상으로 존재하지만, 온도가 계속 증가하면 상분리되어 LCST(lower critical solution temperature)를 나타낸다[1]. 이러한 승온에 의한 상분리 거동에서 외부전장을 가하면 전기활성 고분자인 PVDF에 영향을 주어 상분리 거동이 변화될 것으로 예산된다. (중략)

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