• 한국환경과학회지
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• 제23권7호
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• pp.1289-1297
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• 2014

In this study, PVC-LMO beads were prepared by immobilizing lithium manganese oxide (LMO) with poly vinyl chloride (PVC) diluted in dioxane solvent. XRD and SEM analysis confirmed that LMO was immobilized well in PVC-LMO beads. The diameter of PVC-LMO beads prepared by dioxane solvent was about 2 mm. The adsorption experiments of lithium ions by PVC-LMO beads were conducted batchwise. The optimum pH was pH 10. The adsorption characteristics of lithium ions by PVC-LMO beads was well described by the pseudo-second-order kinetic model. The maximum adsorption capacity obtained from Langmuir model was 24.25 mg/g. The thermodynamic parameters such as ${\Delta}H^{\circ}$, ${\Delta}S^{\circ}$ and ${\Delta}G^{\circ}$ were evaluated. The calculated ${\Delta}G^{\circ}$ was between -6.16 and -4.14 kJ/mol (below zero), indicating the spontaneous nature of $Li^+$ adsorption on PVC-LMO beads. Also, the results showed that PVC-LMO beads prepared in this study could be used for the removal of lithium ions from seawater containing coexisting ions such as $Na^+$, $K^+$, $Mg^{2+}$ and $Ca^{2+}$.

• 공업화학
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• 제16권4호
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• pp.513-518
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• 2005

혼합비율 및 반응온도의 변화에 따른 ZnO가 첨가된 PVC와 PS의 혼합 열분해 특성에 관한 연구를 TG와 GC-MS를 이용하여 수행하였다. 본 연구로부터 혼합물에 있어서 PS의 양이 증가할수록 액상 생성물은 증가하였으며 기상 생성물은 감소함을 알 수 있었다. 또한 ZnO의 첨가량이 증가할수록 기상 생성물과 염화수소의 발생량은 감소하였으며 염화수소의 발생 억제 및 액상 생성물의 최대수율을 얻기 위한 최적의 반응온도는 $500^{\circ}C$임을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제26권1호
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• pp.51-56
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• 2005

A PVC membrane electrode for lead ion based on 1-phenyl-2-(2-quinolyl)-1,2-dioxo-2-(4-bromo) phenylhydrazone (PQDBP) as ionophore was demonstrated. The optimum composition of the membrane was 30 wt% poly(vinyl chloride), 60 wt% dibutyl phthalate as a plasticizer, 4 wt% ionophore and 6 wt% sodium tetraphenylborate as additive. The electrode exhibits a Nernstian response (28.7 mV decade$^{-1}$) for Pb$^{2+}$ over a wide concentration range (1.0 ${\times}$ 10$^{-1}$ to 1 ${\times}$ 10$^{-6}$ M) with a detection limit of 6.0 ${\times}$ 10$^{-7}$ M. This sensor has a short response time and can be used for at least 2 months without any divergence in potentials. The proposed electrode could be used in a pH range of 3.0-6.0 and revealed good selectivities for Pb$^{+2}$ over a wide variety of other metal ions. It was successfully applied as an indicator electrode for the potentiometric titration of lead ion with potassium chromate and for the direct determination of lead in mine.

• Bulletin of the Korean Chemical Society
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• 제24권10호
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• pp.1485-1489
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• 2003

The gelation for di-(2-ethylhexyl) phthalate (DEHP)-plasticized poly(vinyl chloride) was studied by measuring time-resolved small-angle X-ray scattering (SAXS) and a flow of the solutions in test tube. It was found that for the gelation there were three regimes. At Regime I, the solution rapidly changed to a gel, and the SAXS intensity showed a peak and the peak intensity increased, keeping the peak angle constant. Applying the SAXS intensity to the kinetic analysis of the liquid-liquid phase separation, it was revealed that the spinodal decomposition proceeded to develop a periodic length of 29.9 nanometer in size, a hydrogen-bonding-type association in polymer rich phase followed, and then it induced fast gelation rate. At Regime II, the gelation slowly occurred and the SAXS intensity was not observed, suggesting that a homogeneous gel network was formed by a hydrogen-bonding. At regime III, the solution was a homogeneous sol.

• 보존과학연구
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• 통권14호
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• pp.35-44
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• 1993

The way of prevention for the continuous corrosion progress in iron antiquities after excavation and conservation treatment have been studied. The corrosion occuring have been found the oxidation of ferrous ions in the presence of chloride. The consideration to control the activity of chloride is important of controling relative humidity for the stable environment of the storage. One of the method that keeps archeological iron antiquities recommend the storage of special vinyl film(poly-vinyl alcohol film) with silica gel to control the relative humidity. Although this method is not permanent, it's very well efficiency of economy and convenience at present.

• Fibers and Polymers
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• 제3권1호
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• pp.14-17
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• 2002

Development of a novel fixed site carrier membrane (FCM), supported by PET fabric for metal ion separation is reported. The membranes were prepared by dipping PET fabric into the methylene chloride solution of Poly(5-vinyl-m-phe-nylene-m'-phenylene-32-crown-10) (P(VCE)), a polymeric metal ion carrier. It was found that the flux of mono-valent metal ion transported across the membrane is signif=cantly differed from each other and the flux decreases in the order $Cs^+$>$Rb^+$>$K^+$>$Na^+$>$Li^+$ irrespective to the anion except perchlorate anion. It was explained in terms of the stability of the complex, formed by crown ether unit of the P(VCE) and the various metal ions, meanwhile, the lower rate of transport in the presence of perchlorate anion was ascribed to its low hydrophilicity.

• 한국염색가공학회지
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• 제3권2호
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• pp.43-48
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• 1991

Cellulose acetate (CA) and poly-4-vinyl pyridine (PVP) in various weight proportions were mixed in a mixed solvent of trifluoroacetic acid: methylene chloride/6:4 (v:v). CA was miscible with PVP in that solvent system. CA/PVP/solvent show liquid crystal in a certain range of concentration and the nature of that liquid crystal was cholesteric. Films of the liquid crystal composite cast from the liquid crystal solutions of CA/PVP were tested in a viewpoint of biomembrane. Results show that considering permselectivity CA/PVP membrane is better than that of CA and CA/PVP membrane is closer to cell membrane.

• 멤브레인
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• 제20권2호
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• pp.169-172
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• 2010

Poly(vinyl chloride)-g-poly(styrene sulfonic acid) (PVC-g-PSSA) 가지형 공중합체를 합성한 후, 이를 이용하여 $80^{\circ}C$에서 열적으로 환원하여 은 나노입자를 제조하였다. 반응 시간을 바꿈에 따라 다양한 구조의 은 나노입자를 제조하는데 성공하였다. 1시간 정도의 짧은 반응 시간에서는 가지형 공중합체의 미세 상분리 구조를 크게 변화시키지 않고 5 nm 크기의 작은 은 나노입자가 생성되었다. 5시간 정도의 중간 반응 시간에서는 30 내지 50 nm 정도의 크기를 갖는 은 나노입자가 생성되었다. 18시간 정도의 긴 반응 시간에서는, 은입자가 뭉친 허리케인 모양의 은 집합체가 관찰되었다.

• 폴리머
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• 제35권6호
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• pp.615-618
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• 2011

탄소나노튜브(CNT)는 뛰어난 전기적, 물리적인 특성으로 인해 차세대 소재로서 관심을 끌어 왔다. 그러나 탄소나노튜브들 사이에는 본질적으로 강한 소수성 상호작용이 내재하여 불규칙한 결합체를 생성하기 때문에 다양한 분야로의 응용이 어려웠다. 본 연구에서는 양친성 가지형 공중합체, poly(vinyl chloride)-graft-poly(oxyethylene methacrylate), PVC-g-POEM를 합성하였고 극성 용매에서 단일벽 탄소나노튜브를 분산시킬 수 있는 용이한 방법을 제시하였다. PVC-g-POEM는 원자전달 라디칼중합(ATRP)으로 중합되었고 gel permeation chromatography(GPC)와 $^1H$ NMR spectroscopy를 통해 성공적인 합성되었음을 확인하였다. 단일벽 탄소나노튜브는 분산제인 PVC-g-POEM와의 친화력으로 인해 극성 용매 dimethylsiloxane(DMSO)에서 균일하게 분산되었으며 transmission electron microscopy(TEM) 분석으로 단일벽 탄소나노튜브와 PVC-g-POEM의 상호작용으로 생성된 나노복합체의 분산 형태를 관찰하였다. 또한 용매증발 과정을 거쳐 우수한 균질성을 보이는 free-standing 나노복합체 막을 제조하였다.

• Bulletin of the Korean Chemical Society
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• 제31권10호
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• pp.2918-2922
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• 2010

We demonstrate a facile route to synthesize silver chloride nanocubes and derivative nanomaterials. For the synthesis of silver chloride nanocubes, silver nitrate and hydrochloric acid were used as precursors in ethylene glycol, and poly (vinyl pyrrolidone) as a surfactant. Molar ratio of the two precursors greatly influenced the morphology and composition of the final products. As-synthesized silver chloride nanocubes showed size-dependent optical properties in the visible region of light, which is likely due to a small amount of silver clusters formed on the surface of silver chloride nanocubes. Moreover, we show for the first time that simple reduction of silver chloride nanocubes with different reducing reagents leads to the formation of delicate nanostructures such as cube-shaped silver-nanoparticle aggregates, and silver chloride nanocubes with truncated corners and with silver-nanograin decorated corners. Additionally, we quantitatively investigated for the first time the evolution of silver chloride nanocubes to silver chloride nanocubes decorated with silver nanoparticles upon exposure to e-beam. Our novel and facile synthesis of silver chloride related nanoparticles with delicately controlled morphologies could be an important basis for fabricating efficient photocatalysts and antibacterial materials.