• 제목/요약/키워드: divalent cations

검색결과 154건 처리시간 0.021초

점토광물(粘土鑛物)이 정수(淨水)에 미치는 영향(影響)에 관한 연구(硏究) (A Study on the Effect of clay Minerals on Clarification of Water)

  • 박병윤;최정
    • Current Research on Agriculture and Life Sciences
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    • 제6권
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    • pp.93-97
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    • 1988
  • 경수(硬水)나 오수(汚水)로부터 청정(淸淨)하고 안전(安全)한 음용수(飮用水)를 얻기 위한 기초자료(基礎資料)를 제공할 목적으로 한국산 점토광물(粘土鑛物)(Kaolinite, Montmorillonite)의 이화학적(理化學的) 특성(特性)과 이들에 의한 각종 양이온들의 경쟁흡착(競爭吸着)을 조사(調査)하였다. 양이온들간의 흡착력(吸着力)의 세기는 Kaolinite나 Montmorillonite의 두 점토광물(粘土鑛物) 공(共)히 $Ca^{{+}{+}}$ > $Mg^{{+}{+}}$ > $K^+$ > $Na^+$의 순(順)이었으며 Kerr의 공식에 의한 Montmorillonite에서의 양(陽)이온 선택성계수(選擇性系數)(K)는 $^KCa^{{+}{+}}/K$ > $^KMg^{{+}{+}}/K$, $^KCa^{{+}{+}}/Mg$ > $^KK^+/Mg$의 순(順)이었다. 한편 $Na^+$으로 포화(飽和)된 Montmorillonite의 경우 양(陽)이온의 흡착량(吸着量)이 가장 많았다. 따라서 경수(硬水)나 오수(汚水) 중의 각종 양(陽)이온들을 보다 효과적으로 제거(除去)하기 위해서는 Montmorillonite에 $Na^+$을 포화(飽和)시켜 사용하는 것이 바람직하다고 하겠다.

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Chemical Assessment of Heavy Metal Contamination in Soil

  • Yang, Jae-E.;Choi, Moon-Heon
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 1997년도 총회 및 춘계 학술발표회 논문집
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    • pp.8-11
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    • 1997
  • Current methods of evaluating soil contamination by heavy metals rely on analyzing samples for total contents of metals or quantities recovered in various chemical extracting solutions. Results from these approaches provide only an index for evaluation because these methodologies yield values not directly related to bioavailability of soil-borne metals. In addition, even though concentrations of metals may be less than those required to cause toxic effects to biota, they may cause substantial effects on soil chemical parameters that determine soil quality and sustainable productivity. The objective of this research was to characterize effects of Cu or Cd additions on soil solution chemistry of soil quality indices, such as pH, EC, nutrient cation distribution and quantity/intensity relations (buffer capacity). Metals were added at rates ranging from 0 to 400 mg/kg of soil. Soil solution was sequentially extracted from saturated pastes using vacuum. Concentrations of Cu or Cd remaining in soil solutions were very low as compared to those added to the soils, warranting that most of the added metals were recovered as nonavailable (strongly adsorbed) fractions. Adsorption of the added metals released cations into soil solution causing increases of soluble cation contents and thus ionic strength of soil solution. At metal additions of 200~400 mg/kg, EC of soil solution increased to as much as 2~4 dS/m; salinity levels considered high enough to cause detrimental effects on plant production. More divalent cations (Ca+Mg) than monovalent cations (K+Na) were exchanged by Cu or Cd adsorption. The loss of exchangeable nutrient cations decreased long-term nutrient supplying capacity or each soil. At 100 mg/kg or metal loading, the buffering capacity was decreased by 60%. pH of soil solution decreased linearly with increasing metal loading rates, with a decrement of up to 1.3 units at 400 mg Cu/kg addition. Influences of Cu on each of these soil quality parameters were consistently greater than those of Cd. These effects were of a detrimental nature and large enough in most cases to significantly impact soil productivity. It is clear that new protocols are needed for evaluating potential effects of heavy metal loading of soils.

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Theoretical Studies on Selectivity of Dibenzo-18-Crown-6-Ether for Alkaline Earth Divalent Cations

  • Heo, Ji-Young
    • Bulletin of the Korean Chemical Society
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    • 제33권8호
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    • pp.2669-2674
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    • 2012
  • Crown ether is one of well-known host molecules and able to selectively sequester metal cation. We employed M06-2X density functional theory with IEFPCM and SMD continuum solvation models to study selectivity of dibenzo-18-crown-6-ether (DB18C6) for alkaline earth dications, $Ba^{2+}$, $Sr^{2+}$, $Ca^{2+}$, and $Mg^{2+}$ in the gas phase and in aqueous solution. $Mg^{2+}$ showed predominantly strong binding affinity in the gas phase because of strong polarization of CO bonds by cation. In aqueous solution, binding free energy differences became smaller among these dications. However, $Mg^{2+}$ had the best binding, being incompatible with experimental observations in aqueous solution. The enthalpies of the dication exchange reaction between DB18C6 and water cluster molecules were computed as another estimation of selectivity in aqueous solution. These results also demonstrated that $Mg^{2+}$ bound to DB18C6 better than $Ba^{2+}$. We speculated that the species determining selectivity in water could be 2:1 complexes of two DB18C6s and one dication.

Purification and Characterization of Aspartase from Hafnia alvei

  • Yoon, Moon-Young;Park, Jae-Ho;Choi, Kyong-Jae;Kim, Joung-Mok;Kim, Yeon-Ok;Park, Jon-Bum;Kyong, Jin-Burm
    • BMB Reports
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    • 제31권4호
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    • pp.345-349
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    • 1998
  • Aspartase (EC 4.3.1.1) from Hafnia alvei was purified to homogeneity by a combination of DEAE-cellulose, Red A-agarose, and Sepharose 6B chromatography. The purified enzyme appeared homogeneous on denatured SDS-polyacrylamide gel electrophoresis. The purified enzyme was a tetrameric protein composed of identical subunits with a molecular weight of 55,000 daltons. The optimum pH for the enzymatic reaction was 8.5 and the optimum temperature for maximum activity was $45^{\circ}C$. The enzyme has an absolute requirement of divalent metal ions ($Mg^{2+}$, $Mn^{2+}$) at the alkaline pH. The enzyme, however, was inactivated in the presence of other divalent cations such as $Zn^{2+}$, $Ca^{2+}$. The helical content of the purified enzyme was estimated by CD spectropolarimetry to be 61%.

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금속이온으로 치환된 PVA/SSA 이온교환막의 메탄올 투과특성 연구 (Studies on the Methanol Permeability through PVA/SSA Ion Exchange Membranes Substituted with Various Metal Cations)

  • 이충섭;정선영;전지현;신현수;임지원
    • 멤브레인
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    • 제12권1호
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    • pp.51-53
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    • 2002
  • Poly(vinyl alcohol) (PVA)/sulfosuccinic acid $(SSA)-H^+$ 막은 1가 이온 $Li^+, Na^+,K^ + 2$가 이온 $Mg^{2+}, Ca^{2+},Ba^{2+}, 3$가 이온 $Al^{3+}$로 치환하였다. 또한 $Li^{+}$의 경우 치환도를 화하였다. 금속이온치환의 효과를 알아보기 위하여 Diffusion cell을 이용한 메탄올투과도를 측정하였다. 메탄올투과도를 1가 이온의 경우는 'Salting-out'효과뿐 아니라 electrostatic 가교와 금속 이온의 반응성에 의존한다고 사료되었다. 또한 $Li^+$이온이 경우 치환도에 비례하여 메탄올 투과도가 감소하였는데 이는 'Salting-out'효과에 기인한다고 사료되어진다.

Higher Expression of TRPM7 Channels in Murine Mature B Lymphocytes than Immature Cells

  • Kim, Jin-Kyoung;Ko, Jae-Hong;Nam, Joo-Hyun;Woo, Ji-Eun;Min, Kyeong-Min;Earm, Yung-E;Kim, Sung-Joon
    • The Korean Journal of Physiology and Pharmacology
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    • 제9권2호
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    • pp.69-75
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    • 2005
  • TRPM7, a cation channel protein permeable to various metal ions such as $Mg^{2+}$, is ubiquitously expressed in variety of cells including lymphocytes. The activity of TRPM7 is tightly regulated by intracellular $Mg^{2+}$, thus named $Mg^{2+}$-inhibited cation (MIC) current, and its expression is known to be critical for the viability and proliferation of B lymphocytes. In this study, the level of MIC current was compared between immature (WEHI-231) and mature (Bal-17) B lymphocytes. In both cell types, an intracellular dialysis with $Mg^{2+}$-free solution (140 mM CsCl) induced an outwardly-rectifying MIC current. The peak amplitude of MIC current and the permeability to divalent cation ($Mn^{2+}$) were several fold higher in Bal-17 than WEHI-231. Also, the level of mRNAs for TRPM7, a molecular correspondence of the MIC channel, was significantly higher in Bal-17 cells. The amplitude of MIC was further increased, and the relation between current and voltage became linear under divalent cation-free conditions, demonstrating typical properties of the TRPM7. The stimulation of B cell receptors (BCR) by ligation with antibodies did not change the amplitude of MIC current. Also, increase of extracellular $[Mg^{2+}]_c$ to enhance the $Mg^{2+}$ influx did not affect the BCR ligation-induced death of WEHI-231 cells. Although the level of TRPM7 was not directly related with the cell death of immature B cells, the remarkable difference of TRPM7 might indicate a fundamental change in the permeability to divalent cations during the development of B cells.

원수의 수질화학과 HA의 물리화학적 특성이 막 오염에 미치는 영향 (Effects of Surface Water Chemistry and Physicochemical Characteristics of Humic Acid on Fouling of Membrane)

  • 배진열;한인섭;박성호;신지원
    • 한국물환경학회지
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    • 제21권3호
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    • pp.242-247
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    • 2005
  • In this study, we investigated the removal efficiencies of pollutants and permeate fluxes depending on chemistry of feed water, various molecular weight cut-offs (MWCOs) and materials of membrane, operating pressure. We used seven MWCO membranes of YC0.5, YM1, YM3, YM10, YM30, YM100 and PM30, humic acid solution and surface water as feed water, and examined variation in permeate flux. Results of TOC removal experiment demonstrate that MWCO lower 1,000daltons could remove humic acid effectively. As increasing solution pH and decreasing divalent cations ($Ca^{2+}$) concentration, TOC removal increased. But $UV_{254}$ removal efficiency increased with higher divalent cation concentration and solution pH. Membrane fouling increased with increasing electrolyte (NaCl), divalent cation concentration and decreasing solution pH. In spite of initial permeate flux of the hydrophobic membrane (PM30) was higher than that of the hydrophilic membrane (YM30), flux decline of PM30 was significant during operation. At higher operating pressure, compactness of the cake layer on the membrane surface increased, resulting in gradual increase in hydraulic resistance.

Desalting of papermaking tobacco sheet extract using selective electrodialysis

  • Li, Chuanrun;Ge, Shaolin;Li, Wei;Zhang, Zhao;She, Shike;Huang, Lan;Wang, Yaoming
    • Membrane and Water Treatment
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    • 제8권4호
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    • pp.381-393
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    • 2017
  • The inorganic components in tobacco sheet extract have significant influence on the sensory taste of the cigars and the harmful component delivery in cigarette smoke. To identify the contributions of the divalent inorganic components on harmful components delivery in cigarette smoke, a self-made selective electrodialysis was assembled with monovalent ion-selective ion exchange membranes. The influences of current density and extract content on the desalination performance were investigated. Result indicates that the majorities chloride, nitrate, and sulfate ions were removed, comparing with 50-60% of potassium and only less than 10% of magnesium and calcium ions removed in the investigated current density. The permselectivity of the tested cations across the Selemion CSO cation exchange membranes follows the order: $K^+>Ca^{2+}>Mg^{2+}$. A current density of $15mA/cm^2$ is an optional choice by considering both the energy consumption and separation efficiency. When the extract contents are in the range of 7%-20%, the removal ratios the potassium ions are kept around 60%, while the removal ratios of the calcium and magnesium ions fluctuate in the range of 16-27% and 8-14%, respectively. The tobacco smoke experiments indicated that the divalent metal ions have dual roles for the harmful component delivery in cigarette smoke. The divalent potassium and calcium ions were unfavorable for the total particulate matter emission but beneficial to decrease the HCN delivery in the mainstream cigarette smoke. The selective electrodialysis is a robust technology to decrease the harmful component delivery in cigarette smoke.

Fluorescence Quenching of Norfloxacin by Divalent Transition Metal Cations

  • Park, Hyoung-Ryun;Seo, Jung-Ja;Shin, Sung-Chul;Lee, Hyeong-Su;Bark, Ki-Min
    • Bulletin of the Korean Chemical Society
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    • 제28권9호
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    • pp.1573-1578
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    • 2007
  • Fluorescence quenching of norfloxacin (NOR) by Cu2+, Ni2+, Co2+ and Mn2+ was studied in water. The change in the fluorescence intensity and lifetime was measured as a function of quencher concentration at various temperatures. According to the Stern-Volmer plots, the NOR was quenched both by collisions and complex formation with the same quencher. However, the static quenching had a more important effect on the emission. Large static and dynamic quenching constants support significant ion-dipole and orbital-orbital interactions between NOR and cations. The both quenching constants by Cu2+ were the largest among quenchers. Also, quenching mechanism of Cu2+ was somewhat different. The change in the absorption spectra due to the quencher provided information on static quenching. The fluorescence of NOR was relatively insensitive to both the dynamic and static quenching compared with other quinolone antibiotics. This property can be explained by the twisted intramolecular charge transfer.

Effect of Extracellular Cations on the Cehmotherapeutic Efficacy of Anticancer Drugs

  • Park, Sun-Mi;Han, Sang-Bae;Hong, Dong-Ho;Lee, Chang-Woo;Park, Se-Hyung;Jeon, Young-Jin;Kim, Hwan-Mook
    • Archives of Pharmacal Research
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    • 제23권1호
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    • pp.59-65
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    • 2000
  • Cancer development and the efficiency of chemotherapy relies on the patients calcium-related pathological status such as hyper- or hypocalcemica. In the present study, we investigated the effect of extracellular cations such as calcium and magnesium on the therapeutic efficacy of antitumor drugs. The analytic parameters used were cellular drug uptake/excretion and the chemosensitivity of the human breast cancer cell lines, MCF7 and MCF7/ADR. Both calcium and magnesium ions decreased the membrane permeability of cancer cells, which was determined bycell size analysis. These divalent ions also lowered the drug uptake and the cytoplasmic levels of rhodamine 123 and adriamycin, suggesting that they might interfere with the diffusion of these drugs by modifying the physical properties of the cytoplasmic membrane. The acute cytotoxicity of adriamycin after a short period of incubation correlated with changes in its cytoplasmic level. Our results indicate that these extracellular cations might play an important role in the therapeutic activities of anticancer drugs in cancer patients. These results also provide insight a new aspect of chemotherapy, because they suggest that the therapeutic dose of anti-cancer drugs should be modified in cancer-bearing patients presenting with abnormal blood calcium levels.

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