• 전기화학회지
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• 제12권4호
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• pp.335-341
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• 2009

Organic-inorganic hybrid sol-gel matrices were used as hosts for chloro (5, 10, 15, 20-tetraphenylporphyrinato) cobalt (III) (Co[TPP]Cl), a known ionophore for nitrite. The sol-gel precursor was prepared by the reaction of (3-isocyanopropyl) triethoxysilane with 1,4-butanediol. An appropriate amount of the anion-exchanger, tridodecylmethylammonium chloride (TDMAC) and the plasticizer, tributylphosphate (DBP) were used as membrane additives. On mixing with an acidic catalyst, the sol-state precursors slowly gelled, yielding a membrane in which the active components, Co[TPP]Cl and TDMAC, were encapsulated. The performances of the sol-gel membrane-based electrodes were compared to those of Co[TPP]Cl-based poly(vinyl chloride) (PVC) membrane electrodes. Membranes with a molar ratio of Co[TPP]Cl: TDMAC (1 : 0.1) showed reasonable response slopes toward nitrite. The response slopes were typically 53 mV/decade between $10^{-5.4}$ and $10^{-1.0}\;M$. Selectivities toward nitrite over hydrophilic and small anions such as chloride were somewhat inferior to those observed with PVC-based membranes, but selectivities over lipophilic anions were quite similar. Reduced asymmetry potentials due to protein adsorption were found to occur with the sol-gel matrix relative to PVC-based films when the sensors were employed as a detector in flow-through configuration.

• 공업화학
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• 제28권6호
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• pp.655-662
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• 2017

CdS 및 CdZnS 황화물계 광촉매를 단순 침전법으로 제조하고, 가시광선 조사하에서의 로다민 B 분해반응에 대한 광촉매로서의 활성을 조사하였다. 이때 KCl, NaCl, $K_3PO_4$, $Na_3PO_4$ 등의 4가지 무기염 첨가가 반응에 미치는 영향을 조사하였으며, 특히 광촉매 반응 과정에서의 $K^+$, $Na^+$, $Cl^-$ 그리고 $PO_4{^{3-}}$ 이온의 역할에 중점을 두고 연구를 진행하였다. 첨가되는 무기염들은 전체 광촉매 반응에 큰 영향을 미칠 수 있다는 것을 알 수 있었다. 특히 무기염 중의 양이온에 비해 음이온이 반응속도에 상대적으로 큰 영향을 미치는 것으로 나타났다. 본 연구의 반응조건하에서 $PO_4{^{3-}}$ 음이온은 광촉매 반응속도를 크게 감소시키지만 $Cl^-$ 이온은 오히려 반응속도를 증가시켰다. 따라서 광촉매 반응을 이용한 폐수처리에 있어서는 다른 첨가물질의 영향을 고려하는 것도 필요한 것으로 판단된다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제12권2호
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• pp.55-64
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• 2007

생활 폐기물 매립장 침출수에 의해 오염된 지하수에 포함되어 있는 유기산($C_1-C_6$ aliphatic carboxylic acids)들의 정량 분석을 위해서 짧은 분석시간 안에 무기 음이온 뿐만 아니라 유기산까지 정량이 가능한 ion-exchange chromatography를 이용하여 침출수에 용존되어 있는 유기산을 정성 정량하였고, 검출된 유기산의 특성을 평가하였다. 분석 과정에서 $Cl^$, $Br^-$ 등의 halide 이온들의 유기산에 대한 피크 간섭을 줄이기 위해서 이들을 제거하는 전처리를 시료 주입 전에 적용하였다. 음이온 분석과 동일한 분석조건에서 음이온의 간섭을 최소화 하면서 정량이 가능한 유기산들을 선별하였고, 이들 유기산 중에서 음이온의 간섭을 받지 않는 fomate, acetate, propionate, pyruvate, succinate, oxalate에 대해서 정량 분석을 실시하였다. 본 실험에 사용된 유기산의 linear dynamic range는 0.5 mg/L에서부터 20 mg/L까지로 결정하였다. 이 분석법을 쓰레기 매립지 침출수와 주변 지하수에 대해 용존된 유기산과 무기 이온의 정량에 적용하여 높은 농도의 pyruvate와 낮은 수준의 formate와 acetate가 검출되었다. 지하수의 pyruvate 농도는 $Cl^-$, $HCO_3^-$ 농도와 높은 상관성을 보이고, 매립지에서 멀어질수록 농도가 감소하여, pyruvate는 매립지 침출수로부터 유래되었다고 추정되었다.

• 한국대기환경학회지
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• 제27권5호
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• pp.603-613
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• 2011

The collection of $PM_{10}$ and $PM_{2.5}$ samples was made at Gosan site of Jeju Island. Their ionic compositions of both inorganic and organic phases were then analyzed to examine their acidification and neutralization characteristics in atmospheric aerosols. The mass concentrations of $PM_{10}$ and $PM_{2.5}$ at Gosan site were $37.6{\pm}20.1$ and $22.9{\pm}14.3{\mu}g/m^3$, respectively, showing the content ratio of $PM_{2.5}$ to $PM_{10}$ as 61.0%. In the evaluation of ionic balance, the correlation coefficients (r) between the sums of cationic and anionic equivalent concentrations were excellent with 0.982 ($PM_{10}$) and 0.991 ($PM_{2.5}$). The concentration ratios of $PM_{2.5}/PM_{10}$ derived for nss-$SO_4^{2-}$, $NO_3^-$, and $NH_4^+$ were 0.94, 0.56, and 1.02, respectively, indicating the relative dominance of fine fractions. The acidifying capacity of inorganic anions ($SO_4^{2-}$ and $NO_3^-$) in $PM_{10}$ and $PM_{2.5}$ were 96.5% and 97.3%, while those of organic anions ($HCOO^-$ and $CH_3COO^-$) in each fraction were 2.9% and 2.0%, respectively. On the other hand, the neutralizing capacity of $PM_{10}$ and $PM_{2.5}$ by $NH_3$ were 72.8% and 82.3%, while their $CaCO_3$ counter parts were 22.5% and 13.3%, respectively.

• The Korean Journal of Physiology
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• 제20권2호
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• pp.225-235
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• 1986

가토 근위세뇨관에서 Percoll gradient에 의해 분리한 기저막소포(basolateral membrane vesicle)에서 PAH 이동에 미치는 여러 음이온들의 영향을 rapid filtration technique을 이용하여 관찰하였다. NA-dependent PAH 축적은 용액내 $SO_4$와 $SSO_3$에 의하여 유의하게 억제되었으나 $Cl,\;SCN,\;HPO_4,\;acetate$ 및 oxalate에 의해서는 영향을 받지 않았다. 용액내의 $SO_4$는 상경적으로 PHA 이동을 억제하였다. 소포내 음이온을 부하시킨 후 PAH 이동을 측정했을 때 $acetate,\;SO_4$ 및 PAH의 부하에 의해 PAH 이동은 유의하게 증가되었으며, 소포내 부하되는 $SO_4$농도가 증가함에 따라 PAH 축적은 증가되었다. $SO_4$에 의한 PAH의 trans-stimulation은 Na 농도 경사 존재시 더욱 증가되었으며 이들은 2 mM probenecid 및 1mM SITS에 의해 억제되었다. 이들 결과들은 신피질세뇨관 세포의 기저막에 PAH/음이온 교환에 의해 PAH가 이동되는 기전이 존재한다는 것을 가르킨다. 그러나 PAH 이동에 영향이 없는 음이온들은 PAH/음이온 교환에 기질로써 작용하지 않기 때문인지 아니면 이들 음이온들의 높은 투과성에 인해 나타난 결과인지는 더욱 추구해 보아야 확인될 것으로 생각된다.

• 한국환경보건학회지
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• 제32권4호
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• pp.359-372
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• 2006

In order to investigate the daily deposition characteristics of water-soluble inorganic components in airborne deposit on the Iksan, deposition samples were collected using a deposition gauge from October 16 to November 1, 2004. Deposition samples were collected using two different sampling gauges, a dry gauge and a wet gauge, respectively. To get wet the bottom of wet gauge during the sampling period, the volume of $30{\sim}50ml$ distilled ionized water was added in a wet gauge before the beginning of each deposition sampling. Deposition samples were collected twice a day and analyzed for inorganic water-soluble anions ($Cl^-,\;{NO_3}^-,\;{SO_4}^{2-}$) and cations (${NH_4}^+,\;Na^+,\;K^+,\;Mg^{2+},\;Ca^{2+}$) using ion chromatography. Qualify control and quality assurance of analytical data were checked by the data obtained from reinjection of standard solution, Dionex cross check standard solutions, and random several deposition samples, and measured data was estimated to be reliable. Considering the deposition sample volume, the sampling time, the surface area of sampling container, and the ion concentration measured, the daily deposition amounts for measured ions were calculated in $mg/m^2$. The total daily deposition amounts of all measured ions for dry and wet gauge were $7.5{\pm}2.8$ and $17.7{\pm}4.2mg/m^2$, respectively. A significant increase in deposition amount during rainfall days was observed for both wet gauge and dry gauge, having no difference of deposition amount between in wet gauge and in dry gauge. The mean deposition of all ions measured in this study were higher in wet gauge than in dry gauge because of the surface difference of the sampling container, especially for ${NH_4}^+\;and\;{SO_4}^{2-}$. The mean deposition amounts of ${NH_4}^+\;and\;{SO_4}^{2-}$ in wet gauge were found to be about 10 times and 3 times higher than those in dry gauge, while the rest of the chemical species were equal or a little higher in wet gauge than in dry gauge. Dominant species in dry gauge were ${NO_3}^-\;and\;Ca^{2+}$, accounting for 21% and 28% of the total ion deposition, whereas those in wet gauge were ${SO_4}^{2-}\;and\;{NH_4}^+$, accounting for 19% and 41% of the total ion deposition, respectively.

• 한국염색가공학회지
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• 제7권4호
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• pp.61-73
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• 1995

Inorganic salts have negative or positive effects on the rates of many chemical reactions and also the rates of acidic and alkaline hydrolysis of carboxylic esters. The direction of salt effects on the hydrolysis of ester depends on the charge of esters. It is expected that the rate of the alkaline hydrolysis of Poly(ethylene terephthalte)(PET), polymeric solid carboxytic polyester with carboxyl end group at the polymer end, is also influenced by inorganic salts. In the present work, to clarify the effect of divalent cations on the alkaline hydrolysis of PET, many salts with divalent cations like $MgCl_{2},CaCl_{2},SrCl_{2},BaCl_{2},$ were added to the aqueous alkaline solutions. Then PET was hydrolyzed with aqueous NaOH solution having many salts under various conditions. Some conclusions obtained from the experimental results were summarized as follows. Many salts with various divalent cations increased or decreased the reaction rate of alkaline hydrolysis of PET depending on their electrophilicity, hydration property, ability of ion pair formation, solubility, and the degree of interactions between divalent cations and anions, etc. The hydrolysis was interrupted in the order of $Ca^{+2} and was generally accelerated in the order of $Ba^{+2}. It was inferred from the increase in ΔS$^*$and the decrease in the ΔG$^*$that the divalent cations $Sr^{+2}$ and $Ba^{+2}$attracted by PET increased the collision frequency between carbonyl carbon and $OH^{-}$ion and then accelerated the reaction rate. $Mg^{+2}$and $Ca^{+2}$decreased the reaction rate because of their strong interaction with $OH^{-}$.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1738-1742
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• 2005

In this study a novel triiodide ion-selective electrode based on a charge transfer complex of iodine and Bis(2-hydroxyacetophenone)butane-2,3-dihydrazone (ICT), as a membrane carrier was prepared. The electrode has a linear dynamic range between 1.0 ${\times}$ $10^{-2}$ and 5.0 ${\times}$ $10^{-7}$ M, with a Nernstian slope of 58. 99 ${\pm}$ 0.3 mV $decade^{-1}$ and detection limit of 3.0 ${\times}$ $10 ^{-7}$ M. The potentiometric response of the proposed sensor is independent of the pH of the solution in the pH range of 3.0-10.0. The electrode possesses the advantages of short conditioning time, fast response time, and especially, very good selectivity over a large number of common organic and inorganic anions. The electrode can be used for at least 6 months without any considerable divergences in the potentials. It was used as an indicator electrode in potentiometric titration of triiodide ion with thiosulfate.

• Bulletin of the Korean Chemical Society
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• 제25권2호
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• pp.172-176
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• 2004

A highly selective membrane electrode based on1,3,5-triphenylpyrylium perchlorate (TPPP) is presented. The proposed electrode shows very good selectivity for sulfate ions over a wide variety of common inorganic and organic anions. The sensor displays a nice Nernstian slope of -29.7 mV per decade. The working concentration ranges of the electrode is 1.0{\times}10^{-1}-6.3{\times}10^{-6} $M with a detection limit of $4.0{\times}10^{-6}$ M (480 ng per mL). The response time of the sensor in whole concentration ranges is very short (< 6 s). The response of the sensor is independent on the pH range of 2.5-9.5. The best performance was obtained with a membrane composition of 32% PVC, 59% benzyl acetate, 5% TPPP and 4% hexadecyltrimethylammonium bromide. It was successfully used as an indicator electrode for titration of sulfate ions with barium ions. The electrode was also applied for determination of salbutamol sulfate and paramomycine sulfate.

• Asian Journal of Atmospheric Environment
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• 제6권1호
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• pp.23-32
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• 2012

The ionic composition of $PM_{2.5}$ samples was investigated by their datasets of cationic ($Na^+$, $NH_4^+$, $K^+$, $Mg^{2+}$, and $Ca^{2+}$) and anionic components ($Cl^-$, $NO_3^-$, and $SO_4^{2-}$) along with relevant environmental parameters collected from an urban monitoring site in Korea at hourly intervals in 2010. The mean (and SD) annual concentration of $PM_{2.5}$ was computed as 25.3 ${\mu}g\;m^{-3}$ with the wintertime maximum. In addition, sum concentrations (neq $m^{-3}$) of five cationic species (291) were slightly lower than 3 anionic species (308). Most cations exhibited the highest seasonal values in spring, while anions showed more diversified seasonal patterns. According to PCA, five major source categories were apparent with the relative dominance of secondary inorganic aerosols (SIA). The results of our study suggest consistently that the distribution of ionic constituents in an urban area is affected by the combined effects of both natural and anthropogenic processes.