• Title/Summary/Keyword: ionic calcium

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Effects of Dissolved Humic Acid on Complexation and Activate Carbon Adsorption of PCB (Humic Acid가 PCB의 착화합과 활성탄 흡착특성에 미치는 영향)

  • Kim, Sung-Hyun;Beak, Il-Hyun
    • Applied Chemistry for Engineering
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    • v.4 no.4
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    • pp.746-752
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    • 1993
  • Quantitative measurements have been made by using equilibrium dialysis techniques on the extent of complexation between PCB and dissoved humic acid(HA). This research investigates the effectiveness of activated carbon adsorption for the removal of PCB from organic free water and humid acid background solution by using bench-scale equilibrium and rate tests. It was found that the extent of complexation depended on the pH, calcium concentration, ionic strength, and the concentration of humic acid. When HA was present, activated carbon capacity was greatly reduced due to complexation and competitive adsorption effects and the adsorption characteristics became complicated by the presence of various species such as the unassociated HA, PCB, and PCB-HA complexes.

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Characteristics of $PM_{2.5}$ Particles Measured in the Background Sites of Korea (우리나라 청정 지역에서 측정한 $PM_{2.5}$ 입자의 특성)

  • 이종훈;김용표;문길주;김희강;정용승;이종범
    • Journal of Korean Society for Atmospheric Environment
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    • v.13 no.6
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    • pp.439-450
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    • 1997
  • Atmospheric fine particles $(PM_{2.5})$ were collected at the background sites, Kangwha, Taean, and Kosan and characterized to understand their behaviors at the sites. Daily samples of $PM_{2.5}$ mass were measured and ionic species, carbonaceous species, and gaseous species were analyzed. Four-day backward trajectory analysis was also carried out. The mean concentrations of anthropogenic species were highest at Kangwha among three sites, while contributions from sea salts wree highest at Taean during the measurement period due to higher wind speed at Taean. Major chemical components in fine particles were sulfate, organic carbon, nitrate, and ammoniu. Most of the non-sea-salt (nss) sulfates in $PM_{2.5}$ might be present as ammonium sulfates at these sites. Most air parcels arriving at Kangwha and Taean were from northern China. Therefore, both sites were thought to be affected by the same air parcel. At Kosan, during the measurement period, air parcels were from either northern China or sourthern China. The nss sulfate concentration in the air parcels from southern China was higher, while the nss calcium, nitrate, and ammonium concentrations were higher when the air parcels were from northern China.

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Advanced Membrane Systems for Seawater Desalination. Kinetics of Salts Crystallization from RO Brines Promoted by Polymeric Membranes

  • Curcio, Efrem;Obaidani, Sulaiman Al;Macedonio, Francesca;Profio, Gianluca Di;Gualtieri, Silvia;Drioli, Enrico
    • Membrane Journal
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    • v.17 no.2
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    • pp.93-98
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    • 2007
  • The reliability of innovative membrane contactors technology (i.e. Gas/Liquid Membrane Contactors, Membrane Distillation/Crystallization) is today increasing for seawater desalination processes, where traditional pressure-driven membrane separation units are routinely operated. Furthermore, conventional membrane operations can be integrated with membrane contactors in order to promote possible improvements in process efficiency, operational stability, environmental impact, water quality and cost. Seawater is the most abundant aqueous solution on the earth: the amount of dissolved salts covers about 3% of its composition, and six elements (Na, Mg, Ca, K, Cl, S) account for more than 90% of ionic species. Recent investigations on Membrane Distillation-Crystallization have shown the possibility to achieve significant overall water recovery factors, to limit the brine disposal problem, and to recover valuable salts (i.e. calcium sulphate, sodium chloride, magnesium sulphate) by combining this technology with conventional RO trains. In this work, the kinetics of $CaSO_4{\cdot}2H_2O,\;NaCl\;and\;MgSO_4{\cdot}7H_2O$ crystallization is experimentally investigated in order to improve the design of the membrane-based crystallization unit.

Cation Nonstoichiometry in CaTi$O_3$ (CaTi$O_3$에서 양이온 비화학양론)

  • Han, Yeong-Ho
    • Korean Journal of Materials Research
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    • v.2 no.3
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    • pp.207-212
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    • 1992
  • The defect structure of calcium titanates with CaO excess or $TiO_2$ excess was studied by measuring electrical conductivities as a funcition of oxygen partial pressure at $85O^{\circ}C$ to $1050^{\circ}C$. Execess CaO may divide itself equally between A and B sites, resulting in $Ca_{Ti}$" and Vo", while excess $TiO_2$ form $V_{Ca}$" and Vo". The equilibrium electrical conductivity data indicate that the solubilities of CaO and $TiO_2$ in $CaTiO_3$ are 5000ppm and 2000ppm, respectively. Oxygen vacancies contributed to the ionic conduction which flatten the conductivity minima and did not make any defect association with oppositely charged defects.ely charged defects.

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Complexes of Alkaline Earth Metals with Organic Acids (알칼리토류 금속의 유기산 착물)

  • Choi, Sang Up;Kang, Hi Chun
    • Journal of the Korean Chemical Society
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    • v.16 no.6
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    • pp.354-360
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    • 1972
  • Formation of the complexes of barium, strontium and calcium ions with dibasic organic acid ions in dilute solution was studied at room temperature, utilizing the equilibrium exchange technique which involved the uses of radioactive alkaline earth metal ions and cation excbange resin. The organic acids used in this study were succinic and tartaric acids, and the solvents used were water, 20 % acetone-water and 20 % ethanol-water. The pH of the solutions was controlled to 7.2∼7.4, and the ionic strength of the solutions was kept at approximately 0.1. The experimental results indicated that the alkaline earths formed one-to-one complexes in solution with the dibasic acids examined, and that the relative stabilities of the complexes increased in the order: $Ba^{++}; succinic

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Characteristics of Aerosol Composition at Jeju City, Korea

  • Hu, Chul-Goo;Lee, Ki-Ho;Oh, Tae-Gwon;Kang, Chun-Hee;Yang, Soon-Mi
    • Journal of Environmental Science International
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    • v.12 no.5
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    • pp.541-549
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    • 2003
  • Aerosol measurement were carried out to investigate the characteristics of its chemical composition directly affected by the local emissions of Jeju City, Jeju Island by using an eight-stage cascade impactor from Dec. 1999 to Aug. 2000. The ambient aerosol concentrations measured at Jeju City were generally very low but the fine particle concentrations were to be higher than the US standard of PM2.5. The majority of sulfate were non sea salt and contained in the fine particles. In the fine particles, the concentrations of Na$\^$+/, K$\^$+/, Mg$\^$2+/, Ca$\^$2+/, Cl$\^$-/ and NO$\sub$3$\^$-/ had a tendency to increase during the springtime rather than the other seasons. However, the springtime sulfate and ammonium concentrations in the fine particles were slightly lower than those during the other seasons. On the other hand, associated with the coarse particles, the concentrations of ionic species except potassium and ammonium were elevated during the springtime. The calcium concentrations in the coarse particles were increased up to 8 times relative to the other seasons.

Effect of Fluorides on Mullitization of $SiO_2-Al_2O_3$ System; Korean Kaolin (플루오르화물이 $SiO_2-Al_2O_3$계 원료의 물라이트화에 미치는 영향)

  • 최상욱;이철규
    • Journal of the Korean Ceramic Society
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    • v.17 no.2
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    • pp.61-68
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    • 1980
  • The effect of the addition of various fluoreides on the mullitization of Korean crude kaolin was studied by X-ray powder diffraction and scanning electron microscopic methods. Kaolin without any addition of fluoreides began to be transformed into the mullite at 1, 10$0^{\circ}C$. Mullite peaks were discernible in the X-ray diffraction patterns of the specimens which contained fluorides equivalent to about 2 wt % fluorine, and which were sintered at 1, 05$0^{\circ}C$. The higher the concentration of fluorine in kaolin, the lower was the initiatinig temperature of mullitization. Experiments , for example, showed that mullite could be formed at 95$0^{\circ}C$ from kaolin mixed with 3.4% fluorine. Of the fluoride, addtives, sodiumsiliconfluoride $(Na_2SiF_6)$ was must effective in mullite formation of kaolin. In order of accelerating mullitization, the fluorides except $Na_2SiF_6$ could be placed in following sequence ; (1) sodium (NaF) (2) aluminium$(AlF_3)$ (3)potassium(KF) (4) ammonium$(NH_4F)$ (5) magnesium$(MgF_2)$ (6) calcium$(CaF_2)$. It was considered that the intrinsic characteristics of fluorides, such as size of ionic radiu, charge , bond strength between cation and anion, and electronegativity of cation affected millitization of halloysite, a main constituent mineral of kaolin.

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Systematic study on calcium-dissolved organic matter interaction in a forward osmosis membrane-filtration system (정삼투 멤브레인 공정에서 칼슘이온과 용존 유기물 상호작용에 의한 플럭스 변화 연구)

  • Heo, Jiyong;Han, Jonghun;Kim, Yejin;Her, Namguk
    • Journal of Korean Society of Water and Wastewater
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    • v.30 no.6
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    • pp.737-744
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    • 2016
  • The investigation of effects on fouling propensity with various viscosity of feed solutions would be better understanding for forward osmosis (FO) performance since the fouling propensity was directly influenced with solution viscosity. Therefore, this study was focused on the FO fouling with model foultants (humic acid, alginate) by altering solution viscosity with change of ionic strength (I.S) and $Ca^{2+}$ concentrations. In the comparison between humic acid and alginate, as expected, the alginate generally caused more severe fouling (almost 35.8 % of flux reduction) based on the solution characteristics (high viscosity) and fouling patterns (coil and gel layer). However, interesting point to note is that the fouling propensity of alginate was more severe even though it was applied with low viscosity of feed conditions (I.S = 20 mM, $Ca^{2+}=1mM$). This might be due to that crossed linked gel layer of alginate on the FO membrane surface could be best formed in the condition of $Ca^{2+}$ presence and higher I.S, and that is more dominant to fouling propensity than the low viscosity of feed solutions.

Regulatory Role of Zinc in Immune Cell Signaling

  • Kim, Bonah;Lee, Won-Woo
    • Molecules and Cells
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    • v.44 no.5
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    • pp.335-341
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    • 2021
  • Zinc is an essential micronutrient with crucial roles in multiple facets of biological processes. Dysregulated zinc homeostasis impairs overall immune function and resultantly increases susceptibility to infection. Clinically, zinc supplementation is practiced for treatment of several infectious diseases, such as diarrhea and malaria. Recent focus on zinc as a beneficial element for immune system support has resulted in investigation of the immunomodulatory roles of zinc in a variety of immune cells. Besides its classical role as a cofactor that regulates the structural function of thousands of proteins, accumulating evidence suggests that zinc also acts, in a manner similar to calcium, as an ionic regulator of immune responses via participation as an intracellular messenger in signaling pathways. In this review, we focus on the role of zinc as a signaling molecule in major pathways such as those downstream of Toll-like receptors-, T cell receptor-, and cytokine-mediated signal transduction that regulate the activity and function of monocytes/macrophages and T cells, principal players in the innate and adaptive immune systems.

Variations of Calcium, Bicarbonate, and Cation in the Lacustrine Zone by Interannual Differences in Up-River Discharge

  • An, Kwang-Guk;Lee, Jae-Hoon;Han, Jeong-Ho
    • Korean Journal of Ecology and Environment
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    • v.43 no.4
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    • pp.471-476
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    • 2010
  • Monthly up-river discharge in the riverine zone analysis resulted in large interannual variations and differences in calcium ($Ca^{2+}$), bicarbonate ($HCO_3^-$), and cations in the lacustrine zone (Lz) of Daecheong Reservoir during the wet year (Wy, 1993) vs. dry year (Dy, 1994). Total up-river discharge in the Wy was four times that of the Dy, and the up-river discharge in July~August of the Wy was eight times greater than that of same period of Dy. Annual water retention time in the Lz showed large difference between the two years. Water residence time (WRT) was minimum when the up-river discharge peaked, whereas the WRT was maximum when the up-river discharge was at minimal condition. This peak discharge from the up-river on early July reduced residence time in the Lz on mid-July~late July. Monthly pattern, based on data of May~November, was similar between the two years, but, but mean retention time in the Wy was 50 days shorter than in the Dy. Such hydrology, up-river discharge, and WRT reduced $Ca^{2+}$, $HCO_3^-$, and cations in the Lz. At low up-river discharge in Wy during April~May, the cation content of Ca+Mg+Na+K averaged 1.17meq $L^{-1}$ (range=1.09-1.26meq $L^{-1}$), but as the up-river discharge increased suddenly, the values decreased. Seasonal fluctuations of $Ca^{2+}$ showed exactly same pattern with bicarbonate ion of $HCO_3^-$. The minimum $Ca^{2+}$ (0.03meq $L^{-1}$) was occurred in the early August of wet year and coincided with the minimum $HCO_3^-$. These results suggest that the magnitude of variation in $Ca^{2+}$, bicarbonate, and cations in the lacustrine zone is directly determined by the peak magnitude of up-river discharge. The magnitude of up-river discharge determined water retention time and the magnitude of ionic dilution in the lacustrine zone, resulting in functional changes of the ecosystem.