Earticle

복합 라이너 시스템에서 차수막으로서 PVC 지오멤브레인을 사용하기 위해서는 PVC 지오멤브레인의 침출수내의 화학성분에 대한 화학적 적합성이 중요한 요소이다. 본 논문에서는 0.76mm 두께의 PVC 지오멤브레인이 갖는 합성 일반도시 폐기물 침출수와의 적합성을 실내실험을 통해 살펴보았다. $23^{\circ}C$와 $50^{\circ}C$ 두 가지 경우에 대해 각각 30일, 60일, 90일, 120일 동안 합성 침출수에 PVC 지오멤브레인을 노출시켜 외적형태와 물리적, 역학적 성질의 변화를 측정하였다. 비록 약간의 실험오차와 멤브레인 자체의 불균일성이 존재하지만, 합성된 침출수는 실험에 사용된 PVC 지오멤브레인의 물리적, 역학적 성질을 크게 변화시키지 않았다.

The resistance of flexible PVC geomembranes to leachate chemicals is an important factor when PVC geomembranes are being considered as a barrier layer in a composite liner system. This paper describes laboratory test results that evaluate the chemical compatibility of a 0.76 mm (30 mil) thick flexible PVC geomembrane exposed to a synthetic municipal solid waste (MSW) leachate. Changes in dimensional, physical, and mechanical properties were measured after exposure to the synthetic MSW leachate at $23^{\circ}C$ and $50^{\circ}C$ for 30, 60, 90, and 120 days. Although some variability of the test results is observed due to experimental factors and product variability, the synthetic MSW leachate did not significantly degrade the physical or mechanical properties of the flexible PVC geomembrane. As a result, this paper will conclude the PVC geomembranes are not adversely affected by the synthetic MSW leachate.

본 연구에서는 임피던스 스펙트럼 분석법을 사용하여 중성운반체로 dibenzo-18-crown-6 (D18Cr6)와 valinomycin (Val)을 이용하여 $K^+$이온선택성 PVC막 전극의 막과 용액계면에서의 임피던스 특성을 검토하였다. PVC막에 대한 운반체의 종류와 함량, 가소제, 막두께, 기본전해질의 혼입(doping)여부 및 이온의 농도변화 등을 교류임피던스 분석법을 이용하여 측정하였고, 그 결과를 전극특성과 비교 검토하고 PVC막 전극에서의 전달특성을 규명하였다. 교류 임피던스의 특성을 측정하여 중성운반체로 D18Cr6와 Val을 포함하고 있는 PVC막 전극의 등가회로는 막의 벌크저항과 전기이중층 용량을 포함하는 기하학적용량을 병렬로 하고, 용액저항과 직렬로 구성되는 임피던스의 등가회로임을 확인할 수 있었다. 그러나 저농도 및 저주파수 영역에서 약간의 전하전이저항과 Warburg저항이 나타나 중첩되는 것을 알 수 있었다. $K^+$이온선택성 전극에서 운반체로서 D18Cr6가 Val중 D18Cr6가 기존의 Val보다 전극특성 및 임피던스 특성이 좋았으며 특히 D18Cr6에 기본전해질로 potassium tetraphenylborate (TPB)를 첨가한 경우 이상적인 전극을 제조할 수 있었다. 운반체의 최적 함량은 D18Cr6와 Val의 경우 3.23wt%부근이었고, 가소제는 DBP가 가장 적절하였다. 막두께가 얇아질수록 임피던스 특성이 좋아졌으나, 막두께가 최적 막두께 이하로 얇아지면 전극특성이 나빠짐을 알 수 있었다. D18Cr6의 경우 $K^+$이온에 대한 혼합용액법에 의한 선택계수 서열은 다음과 같았다. $NH_4{^+}>Ca^{2+}>Mg^{2+}>Na^+$.

With impedance spectrum measurements, impedance was studied in the interface between sample solutions for $K^+-ion$ selective PVC membrane electrode containing neutral carriers [dibenzo-18-crown-6 (D18Cr6) and valinomycine (Val)]. Response characteristics of electrode were examined by measuring AC impedance spectra that were resulted from the chemical structure and the content of carrier, variation of plasticizer, membrane thickness, doping of base electrolytes, and concentration variation of sample solution. Transport characteristics of PVC membrane electrode were also studied. It was found that the equivalent circuit for the membrane in $K^+$ solution could be expressed by a series combination of solution resistance and a parallel circuit consisting of the bulk resistance and geometric capacitance of the membrane system. But the charge transfer resistance and Warburg resistance were overlapped a little in the low concentration and low frequency ranges. The carrier, D18Cr6 was best for electrode and impedance characteristics, and ideal electrode characteristics were appeared especially in case of doping of the base electrolyte[potassium tetraphenylborate(TPB)]. The optimum carrier content was about 3.23 wt% in case of D18Cr6 and Val. DBP was best as a plasticizer. As membrane thickness decreased the impedance characteristics was improved, but electrode characteristics were lowered for membrane thickness below the optimum. In the case of D18Cr6, the selectivity coefficients by the mixed solution method for the $K^+$ ion were the order of $NH_4{^+}>Ca^{2+}>Mg^{2+}>Na^+$.

10, 20, 30, and 40% of polyvinyl chloride (PVC) were added to nitrile butadiene rubber (NBR) to modify the latter. The NBR/PVC composites containing pure NBR were synthesized to investigate properties, such as crosslinking density, hardness, tensile strength, abrasion resistance, heat resistance, solvent resistance, and filler dispersion. The experimental result revealed a decrease in crosslinking density and heat resistance with increase in the PVC content. In contrast, addition of PVC to NBR resulted in enhancement of hardness, tensile strength, solvent resistance, and filler dispersion.

The effect of addition of gypsum on the rheology, physico-mechanical properties, thermal properties and morphology development of polymer composites based on polyvinyl chloride (PVC) and waste-gypsum with and without methylene-butadiene-styrene (MBS) has been studied. It was shown that the replacement of gypsum for methylene-butadiene-styrene (MBS) component in PVC/gypsum polymer composites enhanced the tensile strength and stiffness of composites, but gradually decreased its impact strength. The observation of morphology, the results of the physico-mechanical properties and thermal properties proved simultaneously that PVC/gypsum composite with the waste-gypsum content of 22.56 wt% reached the optimum results among five kinds of PVC/gypsum polymer composite materials investigated.

본 실험은 염소계유해유기화합물을 처리하는 목적으로 종래의 초임계수산화법의 결점을 완전히 해결하기 위해서 도달한 것이 질산나트륨을 산화제로서 사용하는 개량된 초임계수 산화법(다단계산화법)이다. 이와 같이 본 연구팀이 개발한 개량된산화법(다단계산화법)은 매우 간단하며 저렴한 염소계유기물 분해처리시스템을 구축하는 것이 가능하다.

Voltammetric characterization of hydrophilic anion transfer processes across a 66 microhole array interface between the water and polyvinylchloride-2-nitrophenyloctylether gel layer is demonstrated. Since the transfer of hydrophilic anions including $Br^-$, $NO_3{^-}$, $I^-$, $SCN^-$ and $ClO_4{^-}$ across the liquid/gel interface usually sets the potential window within a negative potential region, a highly hydrophobic organic electrolyte, tetraoctylammonium tetrakis(pentafluorophenyl)borate, providing a wider potential window was incorporated into the gel phase. The transfer reaction of perchlorate anions across the microhole-water/gel interface was first studied using cyclic voltammetry and differential pulse voltammetry. The full voltammetric response of perchlorate anion transfer was then used as a reference for evaluating the half-wave transfer potentials, the formal transfer potentials and the formal Gibbs transfer energies of more hydrophilic anions such as $Br^-$, $NO_3{^-}$, $I^-$, and $SCN^-$. The current response associated with the perchlorate anion transfer across the micro-water/gel interface versus the perchlorate concentration was also demonstrated for sensing applications.

PET or PVC wig fibers are usually colored by the dope dyeing method in which the pigment or color master batch is mixed before the spinning process. However, the colored fibers need to be dyed again to obtain a two-tone color along the longitudinal fiber direction. In this study, PET and PVC fibers were dyed by the carrier dyeing method using a disperse dye, and the dyeing behavior was investigated. The fiber was dyed at various carrier and dye concentrations. The dye uptake increased with increasing carrier concentration or dye concentration. The saturation of the dye uptake was observed in each case. No change of the glass transition temperature $(T_g)$ was observed in the 1st run of the DSC thermogram, however, a decrease in the value of $T_g$ was observed in the 2nd run performed after the 1st run sample was quenched and re-measured. The reduction in the value of $T_g$ implies that the carrier acted as a plasticizer in the fiber and enhanced the segmental mobility of the polymer chains. The dyeing temperature and carrier concentration were varied and the diffusion coefficients of the dye and activation energy were measured. The activation energy was increased at a higher carrier concentration, because the carrier acted as a plasticizer and lowered the energy barrier to the penetration of the dye molecule into the polymer chains.

The objective of this study was to determine if MWF(metalworking fluids) mass sampled on PVC filter lose during flowing airstream and desiccating and to present direction to correct the underestimated MWF mass. Flowing airstream caused MWF sampled on PVC filter to be breakthrough and lost. Loss of MWF on PVC filter increased in proportion to time of flowing airstream. Meanwhile, loss of MWF was observed during desiccating without flowing airstream. Vapor pressure of MWF is so low that it would not normally be thought to evaporate. However, MWF mist sampled on PVC filter has so great a surface area that loss by flowing airstream and evaporation can be appreciable. Loss between fresh and used MWF was also different. Those study results mean that NIOSH method(#0500 method) to take airborne MWF mist with PVC filter is not valid. Media to sample airborne MWF accurately still have not been introduced. It seems to be needed to estimate how much MWF on PVC filter may be lost during sampling. Regression model between sampling time including 1 day desiccating and total loss of MWF was "Total loss(%)=18.4%+0.06 sampling time(p=0.000, r2=49.6%)". This model help correct MWF lost when one measures airborne MWF using NIOSH # 0500 method.

The sulfonated poly(styrene-divinylbenzene-acrylonitrile) (ST-DVB-AN) composite polymer electrolyte membrane based on the original PVC film was successfully synthesized to improve oxidative stability using semi-interpenetrated polymer network (semi-IPN). Weight gain ratio after copolymerization was enhanced by the DVB and AN contents, and the sulfonated membranes were characterized in terms of proton conductivity (k), ion exchange capacity (IEC), and water uptake ($W_U$). The effect of DVB content and AN addition were thoroughly investigated by comparing the resulted properties including oxidative stability. The obtained ST-DVB-AN composited semi-IPN membranes showed relatively high proton conductivity and IEC compared with Nafion117, and greatly improved oxidative stability of the synthesized membrane was obtained. This study demonstrated that a semi-interpenetrated sulfonated ST-DVB-AN composited membrane reinforced by PVC polymer network is a promising candidate as an inexpensive polymer electrolyte membrane for fuel cell applications.

The biogas holder is composed of an outer membrane and an inner membrane which are subject to outdoor exposure and gas exposure respectively. The influence of weathering conditions on the photo-degradation of a biogas holder was investigated. Tests were performed under three different methods - outdoor exposure tests (Seosan, Arizona), accelerated tests (Xenon-are lamp) with the outer-membrane of biogas. Moreover, the changes in the aging process were monitored using color difference, gloss, the contact angle and an optical microscope. Changes in physical properties, such as decrease reduction in gloss, decrease in the contact angle, increase in color difference were observed in the aging process. The comparison between membrane 3B, 4B and membrane 5B under xenon-arc were discussed. Membrane 5B was very sensitive to ultraviolet (UV) ray. There were many difficulties in the outdoor exposure test due to acid rain, dust, and stain resistance.

A La (III) ion-selective membrane sensor has been fabricated from poly vinyl chloride (PVC) matrix membrane, containing 3-hydroxy-N'-(pyridin-2-ylmethylene)-2-naphthohydrazide (HPMN) as a neutral carrier, potassium tetrakis (p-chlorophenyl) borate (KTpClPB) as an anionic excluder and ortho-nitrophenyloctyl ether (NPOE) as a plasticizing solvent mediator. The effects of membrane composition and pH as well as the influence of the anionic additive on the response properties were investigated. The sensor with 30% PVC, 62% solvent mediator, 6% ionophore and 2% anionic additive, shows the best potentiometric response characteristics. It displays a Nernstian behavior (19.2 mV per decade) across the range of $1.0{\times}10^{-2}-1.0{\times}10^{-7}$ M. The detection limit of the electrode is $7.0{\times}10^{-8}$ M ($\sim$10 ng/mL) and the response time is 15 s from $1.0{\times}10^{-2}$ up to $1.0{\times}10^{-4} $M and 30 s in the range of $1.0 {\times}10^{-5}-1.0{\times}10^{-7}$ M. The sensor can be used in the pH values of 3.0-9.0 for about seven weeks. The membrane sensor was used as an indicator electrode in the potentiometric titration of lanthanum ions with EDTA. It was successfully applied to the lanthanum determination in some mouth wash preparations.

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.

황화이온검출기로서 2가지 형태의 연속 flow-through 전극계의 분석적 감응성질을 조사하고, 최적조건에서 그들의 감응특성을 직접 비교하였다. 두 검출계에 있어서 측정한 봉우리전위를 황화이온농도의 대수값과 관련지웠으며, 적어도 시간당 20개의 시료를 정량할 수 있었다. pH전극법에서는 투석기를 지나 흘러가는 recipient stream의 pH를 측정하였다. 장치는 연속흐름형의 기체투석기가 관형 polymer 막전극과 연결되도록 설계되어 있다. 이 방법의 최적실험조건은 recipient $5.0 {\times} 10^{-5} M NaOH ＋ 5.0 {\times} 10^{-3} M$ NaCl과 diluent 0.10M $H_2SO_4$이며, recipient stream, diluent stream 및 시료의 유속은 모두 1.0ml/min이다. 황화이온 전극법에서는 시판하는 황화이온선택성 전극을 flow-through cell 속의 황화이온을 검출하는 데에 썼다. 이 방법의 최적실험조건인 황화이온 산화방지 완충제(1.0M NaOH 용액에 3.5g 아스코르브산과 7.6g $Na_2EDTA$를 용해)와 시료의 유속은 각각 1.4 ml/min와 1.0 ml/min이다.

The analytical response properties of two types of continuous flow-through electrode system as fulfide ion detectors are examined and directly compared their reponse characteristics under the optimal conditions. In both detection systems, observed peak potentials are logarithmically related to the sulfide ion concentration and at least twenty samples per hour can be determined. In the pH electrode method, the pH of the flowing recipient stream leaving the dialyzer was monitored. The designed system involves the use of continuous flow gas dialyzer in conjunction with the tubular polymer membrane electrode. In this method, optimal experimental conditions are recipient of mixture of $5.0 {\times} 10^{-5} M NaOH ＋ 5.0 {\times} 10^{-3} M$ NaCl and diluent of 0.10 M $H_2SO_4$, and all flow rates of recipient stream, diluent stream, and sample are 1.0 ml/min. In the sulfide ion electrode method, a commercially available sulfide ion-selective electrode was used to detect sulfide ion in the flow-through cell. The optimal flow rates of sulfide anti-oxidant buffer (3.5 g ascorbic acid and 7.6 g $Na_2EDTA$ dissolved in 1.0 M NaOH solution 1 l) and sample were 1.4 ml/min and 1.0 ml/min, respectively.

새로운 管形 PVC膜 질산이온 選擇性 電極을 제작하여 그 性能을 조사하였다. 電極膜의 組成을 5${\%}$ aliquat-NO$_3$ 용액+ 32${\%}$ poly(vinyl chloride) + 63${\%}$ dibutyl sebecate로 하였을 때 전극의 感應特性이 최적이었으며, 이 때의 감응기울기는 58.5 ${\pm}$ 0.1 mV/decade, 檢出限界는 0.02mM, 感應時間 (t$_{99}$)은 25초이었다. 이 전극을 써서 아질산이온을 連續${\cdot}$自動化法으로 정량하였다. Recipient 용액은 pH 7.6의 10$^{-2}$ M 燐酸鹽 緩衝溶液을 쓰고, 여기에 酸化劑로서 過酸化水素를 0.3${\%}$가 되도록 포함시켰다. 전극계의 最適條件에서 아질산이온 標集溶液 8.0 ${\times}$ 10$^{-5}$ M ∼ 5.0 ${\times}$ 10$^{-2}$ M의 범위에서 직선적인 감응을 나타내었으며, 이 때의 감응기울기는 56.8 ${\pm}$ 0.2 mV/decade이었다.

A new tubular poly(vinyl chloride) membrane type of nitrate selective electrode was prepared and its characteristics were evaluated. The response slope, detection limit, and response time (t$_{99}$) under the optimum membrane composition (5${\%}$ aliquat-NO$_3$ solution + 32${\%}$ poly(vinyl chloride) + 63${\%}$ dibutyl sebecate) of the electrode were 58.5 ${\pm}$ 0.1 mV/decade, 2.0 ${\times}$ 10$^{-5}$ M, and 25 seconds, respectively. The nitrite ion was determined by the continuous-automated method using the new electrode. 10$^{-2}$ M phosphate buffer solution (pH 7.6) was used as a recipient solution. And also hydrogen peroxide (0.3${\%}$) was added to the recipient as an oxidant. The linear response range and response range and response slope for the standard nitrite solution under the optimum condition of this electrode system were 8.0 ${\times}$ 10$^{-5}$ M ∼ 5.0 ${\times}$ 10$^{-2}$ M and 56.8 ${\pm}$ 0.2 mV/decade, respectively.