• Title/Summary/Keyword: poly(vinyl alcohol) solution

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Preparation of PVA gel beads by Immobilization of HTTA and TOPO on PVA as Solid Phase Extractant and Removal Characteristics of Copper Ions from Aqueous Solution (고체상 추출제로서 폴리비닐알콜에 테노일트리플루오로아세톤과 트리옥틸포스핀 옥사이드를 고정화한 폴리비닐알콜 겔비드의 제조와 수중의 구리이온 제거 특성)

  • You, Hae-Na;Lee, Min-Gyu
    • Clean Technology
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    • v.20 no.3
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    • pp.251-255
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    • 2014
  • PVA gel beads were made by immobilization of thenoyltrifluoroacetone (HTTA) and trioctylphoshineoxide (TOPO) with poly vinyl alcohol (PVA). The prepared PVA gel beads were used for the removal of $Cu^{2+}$ from aqueous solution. The removal characteristics of $Cu^{2+}$ by PVA gel beads was found to follow the pseudo-second-order kinetic equation. The maximum removal capacity calculated from Langmuir isotherm equation was 9.59 mg/g. The optimal pH was in the range of 3.5~6. Even when the PVA gel beads were reused 5 times, the leakage of extractant and the damage of PVA gel beads was not observed.

Preparation of High Molecular Weight Atactic Poly(vinyl alcohol) Hydrogel by Electron Beam Irradiation Technique (전자빔 조사를 이용한 고분자량 혼성배열 폴리(비닐 알코올) 수화젤의 제조)

  • Kim, Kyung-Sik;Lee, Young-Jae;Lyoo, Won-Seok;Noh, Seok-Kyun
    • Polymer(Korea)
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    • v.32 no.6
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    • pp.587-592
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    • 2008
  • High molecular weight poly(vinyl alcohol) (PVA) hydrogel to be expected as a candidate material for the wound-dressing was successfully prepared by electron beam (EB) irradiation. To produce PVA hydrogels with various gel fractions, degrees of swelling in water, gel strengths, and elongations, two different number-average degrees of polymerization [($P_n$)s] of PVA were adapted such as 1700 and 4000, and the PVA solution concentration and irradiation dose of EB were controlled to range of 5 $\sim$ 20% and 30 $\sim$ 100 kGy, respectively. The gel fraction and strength of PV A hydrogel were increased with increasing molecular weight of PVA, solution concentration, and irradiation dose of EB. On the contrary, the degree of swelling and elongation of PVA hydrogel were decreased. The thermal property and crystallinity related to degree of crosslinking of PVA hydrogel were examined by the analyses of differential scanning calorimetry and X-ray diffraction.

Gas Permeation Properties of Polymeric Membranes for Biosensor Prepared from Poly(vinyl chloride) Derivatives (Poly(vinyl chloride) 유도체로부터 제조된 바이오센서용 고분자막의 기체 투과특성)

  • Lim, Chun-Won;Kim, Wan-Young;Lee, Youn-Sik;Yoon, Jeong-Won;Jeong, Yong-Seob
    • Applied Chemistry for Engineering
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    • v.10 no.3
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    • pp.362-366
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    • 1999
  • Membranes for biosensor were prepared from poly(vinyl chloride) (PVC)l derivatives using the solution casting method, and their gas permeabilities were studied. The polymer membranes dried slowly in air showed higher permeability coefficients than those dried in vacuum. The permeabilily coefficients of carboxylated poly(vinyl chloride) (CPVC) membranes for $O_2$ and $CO_2$ decreased as the pressure of the feed gas increased. The addition of dioctylphthalate (DOP) enhanced the permeation rates for $O_2$ and $CO_2$. For example, the permeability coefficients of CPVC membranes containing 30 wt. % DOP for $O_2$ and $CO_2$ at 100 psig were 2.03 and 0.96 Barrer, respectively, which were about 4~5 times higher than those of the membranes without DOP. Poly(vinyl chloride-co-vinyl acetate-co-vinyl alcohol) (Syn-PVCAcAl) obtained by hydrolysis of poly(vinyl chloride-co-vinyl acetate (PVCA) showed a higher permeability coefficient for $CO_2$ in the presence of DOP than that for commercial PVCAcAl, but did not show any significant difference in permeability for $O_2$.

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Properties and Structure of Poly(vinyl Alcohol) Film Containing Electrolytes

  • Iwaseya, Masato;Yamaura, Kazuo;Dai, Lixing
    • Proceedings of the Korean Fiber Society Conference
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    • 2003.10a
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    • pp.99-99
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    • 2003
  • We have investigated the properties of poly (vinyl alcohol)-film obtained by casting from the solution PVA/electrolytes (NaCl, KCl, MgCl$_2$, CaCl$_2$)/water systems at room temperature. The removed electrolytes films have got high crystallinity as well as high draw ratio. The removed electrolytes films had layer-structure while a film without electrolytes didn't have it. A relation between draw ratio and thickness or number of layers, were recognized.

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Poly(vinyl alcohol) based Solid Polymer Electrolyte with Fast Cationic Transport Process

  • Jo, Yun-Kyung;Lee, Yu-Jin;Jo, Nam-Ju
    • Proceedings of the Polymer Society of Korea Conference
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    • 2006.10a
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    • pp.187-187
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    • 2006
  • A new type solid polymer electrolyte (SPE) composed of poly (vinyl alcohol) (PVA) and lithium trifluoromethanesulfonate ($LiCF_{3}SO_{3}$) was prepared by means of the solution cast technique to observe that Li ion can move by ion hopping decoupled from polymer segmental motion inside of the 'fast cationic transport process'. The highest ion conductivity of the SPEs obtained from ac impedance measurements was $1.42{\times}10^{-3}S/cm$ at room temperature for SPE with 80wt% of salt concentration. Using LSV, we found that the SPEs had good electrochemical stabilities and using FT-IR and AFM, we found the formation of network-like structure.

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Effect of Stereoregularity on the Properties of Syndiotacticity-Rich Ultrahigh Molecular Weight Poly(vinyl alcohol)/Dimethylsu1foxide/Water Gel

  • Park, Jin-Hyun;Lyoo, Won-Seok;Ko, Sohk-Won
    • Proceedings of the Korean Fiber Society Conference
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    • 1998.10a
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    • pp.13-16
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    • 1998
  • Poly(vinyl alcohol) (PVA) gels are easily formed via physical pathway. Most PVA solutions including PVA/water solution are well known to form thermally reversible gels at low temperature but these gels showed poor mechanical properties. In order to overcome this weak point, transparent crosslinked PVA hydrogels were prepared by electron beam irradiation or by chemical process with crosslinking agents or additives. (omitted)

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Effect of Inorganic Nanomater ials on the Morphology and Thermal Proper ties of PVA Nanocomposite Nanowebs

  • Choi, Jae-Young;Yeum, Jeong-Hyun
    • Textile Coloration and Finishing
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    • v.23 no.2
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    • pp.83-89
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    • 2011
  • Poly(vinyl alcohol) (PVA), PVA/Montmorillonite (MMT), PVA/Silver (Ag), and PVA/MMT/Ag nanocomposite nanowebs were prepared by electrospinning technique in aqueous solution. In order to investigate the effect of inorganic materials on the morphology and thermal properties of PVA based nanocomposite nanowebs, experiments were performed with 5 wt.% of MMT and Ag. Field emission type scanning electron microscopy, transmission electron microscopy (TEM), reflection type X-ray diffraction (XRD), and thermal gravimetric analyzer were utilized to characterize nanocomposite nanowebs. TEM and XRD results show MMT and Ag were well dispersed in PVA nanowebs. Those inorganic nanoparticles enhanced thermal property of the nanocomposite nanowebs.

Sputtering of Silk Fabric Using Poly(vinyl alcohol) Binder (폴리비닐알코올 호제를 이용한 실크직물의 Sputtering)

  • Choi, Jae-Woo;Koo, Kang;Son, Hong-Rak;Lyoo, Won-Seok
    • Textile Coloration and Finishing
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    • v.13 no.1
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    • pp.32-37
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    • 2001
  • Silk fabric was sputter-treated with Au, Cu, SUS, and Ti using poly(vinyl alcohol) (PVA) as a binder, and its changes in color, antielectrostatic property, airpermearbility, and rubbing fastness were investigated. Sputter-treated silk fabric had a natural color of metal target, which was deepened by treatment of PVA solution. The rubbing fastness of thin metal layer formed by sputtering was improved by PVA treatment. Au had highest rubbing fastness among the metal targets. In addition, PVA treatment posterior to sputtering resulted In higher rubbing fastness than the other treatment method. However, a reverse trend was found in antielectrostatic property. Air permeability of the sputter-treated silk fabric was improved by PVA treatment, which was highest when sputtering was conducted prior to PVA treatment.

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Pervaporation Separation of Water-Acetic Acid Mixtures Through Poly(vinyl alcohol) Membranes Crosslinked with Glutaraldehyde

  • Yeom, Choong-Kyun;Lee, Kew-Ho
    • Proceedings of the Membrane Society of Korea Conference
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    • 1994.10a
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    • pp.32-33
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    • 1994
  • Poly(vinyl alcohol)(PVA) membranes crosslinked with Glutaraldehyde (GA) were prepared for the separation of acetic acid-water mixtures. For the preparation of the crosslinked membranes, dry PVA films were immersed for 2 days at 40$\circ$C in reaction solutions which contain different content of GA solution(25% GA in water), aceton and a catalyst, HCl. IR spectroscopy was employed to characterize the crosslinking reaction between hydroxyl groups in PVA and aldehyde groups in GA. Swelling measurements of the crosslinked membranes were carried out in both water and acetic acid to investigate the crosslinking density and swelling behaviour of the membranes.

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Shear-induced color transition of PDA (polydiacetylene) liposome in polymeric solutions

  • Lee, Sung-Sik;Chae, Eun-Hyuk;Ahn, Dong-June;Ahn, Kyung-Hyun;Yeo, Jong-Kee
    • Korea-Australia Rheology Journal
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    • v.19 no.1
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    • pp.43-47
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    • 2007
  • The polydiacethylene (PDA) is known to change its color by mechanical shear. The shear-induced color transition has been reported with elastomer or film type of PDA. In this paper, we newly investigated the transition with liposome type of PDAs in polymeric solutions. The liposomes were dispersed in Poly(vinyl alcohol) 2% + Sodium borate 1%, Poly(vinyl alcohol) 15% and Hyaluronic acid 1% (PVA/B, PVA, HA). The shear stress was continuously imposed to each solution by stress control type rheometer with coni-cylinder fixture. The degree of color transition was quantified with the characteristic absorbance peak at 540 nm (blue) and 640 nm (red). As a result, PDA liposome in PVA/B solution changed the color from blue to red upon increasing the magnitude of shear (from 0 to 100 Pa) and the duration of shear-imposed time (from 0 to 5400 sec). Meanwhile, PDA liposome in HA or PVA solution did not noticeably change the color, even though the low shear viscosities of the solutions were kept almost constant. This color transition of PDA liposome is expected to measure the magnitude of shear, and to distinguish different responses of polymeric solutions to the applied shear.