• Title/Summary/Keyword: Ca-ion concentration

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The Spreading Characteristics of the (Polymer/18-Crown-6) Composite Solution for Water Cast-Membranes ((Polymer/18-Crown-6)복합박막 제조용액의 수면전개 특성)

  • 남석태;최호상;최성부;김병식
    • Membrane Journal
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    • v.6 no.4
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    • pp.265-272
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    • 1996
  • The (polymer/carrier) composite membranes for separating the metallic ion have been prepared by the water cast-method. The morphology of these membranes was affected by the physical properties of the spreading solution. The surface tension of the (polymer/18-crown-6) composite solution was decreased with increasing the concentration of 18-crown-6 compound and the surface tension of polymer solution decreased the following order PVC>PS>CA. The viscosity of CA solution decreased with increasing the contents of the 18-crown-6 compound, but PVC and PS solutions showed no significance changes according as the concentration of 18-crown-6 compound. In the composite solutions, the spreading ability was improved by' the cyclic 18-crown-6 molecules which acted as an electric buffer and diminished the intermolecular force between the polymer chains. The (polymer/18-crown-6) composite membrane was more uniform than that of the mono polymer membrane on the coagulation state of polymer, and the top and bottom sides of membrane showed also the more smooth structure according as the concentration increment of 18-crown-6 molecule.

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Properties of Low-Molecular Alginate by Ultrasound

  • Kim Sang-Moo;Park Seong-Min;Lee Keun-Tae;Bae Tae-Jin
    • Fisheries and Aquatic Sciences
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    • v.2 no.2
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    • pp.149-154
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    • 1999
  • Response Surface Methodology was applied for optimizing the processing parameters of ultrasound treatment in order to produce low-molecular alginate. The use of ultrasound significantly reduced viscosity of alginate solutions. Suggested parameters of ultrasound treatment for maximum reduction of alginate molecular weight were: specific intensity, 115.81 $W/cm^2$ at 20kHz frequency; treatment time, 35.55 min; temperature, $20.08^{\circ}C$; alginate concentration, $2.5\%$. Low-molecular alginate obtained by ultrasound had two peaks on Sepharose CL-6B gel filtration. The viscosities of control, fraction I, and fraction II at $0.1\%$ concentration and $25^{\circ}C$ were 3.07, 1.23, and 0.82cps, respectively. Molecular weights of control, fraction I, and fraction II alginates were 336,500, 70,400, and 52,800 daltons, and their solubilities were 3, 6, and $14\%$, respectively. The lower molecular weight of alginate, the lower the alcohol precipitation and the higher $Ca^{2+}$ ion binding capacities. Heavy metal ion binding capacities of alginates were high in the following order of Pb, Cd, Zn, and Co.

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Lipophilic Crown-4 Derivatives as Lithium Ionophores for Lithium Ion Selective Liquid Membrane Electrodes

  • Jae Sang Kim;Sung Ouk Jung;Shim Sung Lee;Si-Joong Kim
    • Bulletin of the Korean Chemical Society
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    • v.14 no.1
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    • pp.123-127
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    • 1993
  • New lipophilic Crown-4 compounds of 16-membered rings containing furan (neutral carrier,I), tetrahydrofuran (neutral carrier,II) and lithium complex of the latter (neutral carrier,III) have been synthesized and tested as the active sensors for lithium ion in poly(vinyl chloride) (PVC) membrane electrode, in the presence and absence of an anion excluder, tetrakis(4-chloro-phenyl)borate (KTClPB), 2-nitrophenyl phenyl ether (NPPE), tris(2-ethylhexyl)phosphate (TEHP), o-nitrophenyl octyl ether (NPOE), dioctyl adipate (DOA), bis(2-ethylhexyl)adipate (BEHA), di-n-octylphenyl phosphonate (DOPP) were used as plasticizing solvent mediators. The electrode response function had a nearly Nernstian slope of 54-61 mV per decade (25$^{\circ}$C) within the concentration range of $10^{-1}-10^{-4}$ M LiCl and the detection limits for all electrodes were ca. $5{\times}10^{-4}$ M. The response time of the electrode was faster at the higher lithium concentration and the response of the electrode was stable for longer than 6 months. The sensor membranes exhibit improved response times and increased lifetimes as compared to the system described earlier.

Nutrient Dynamics in the Throughfall, Stemflow and Soil Solution of Korean Pine, Japanese Larch and Hardwood Stands at Kwangju-Gun, Kyonggi-Do (경기도(京畿道) 광주(廣州) 지방(地方) 잣나무림(林), 낙엽송림(落葉松林), 활엽수림(闊葉樹林)에서 수관통과우(樹冠通過雨), 수간류(樹幹流), 토양수내(土壤水內) 양료동태(養料動態))

  • Park, Yeong Dae;Lee, Don Koo;Kim, Dong Yeob
    • Journal of Korean Society of Forest Science
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    • v.88 no.4
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    • pp.541-554
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    • 1999
  • The objectives of this study were to examine the amount of nutrient input by throughfall and stemflow, and the nutrient dynamics by throughfall, stemflow and soil solution among Piuns koraiensis, Larix leptolepis and hardwood forests including oaks at Kwangju-Gun, Kyonggi-Do. A total amount of rainfall during the study period was 1410.1mm. Of the total rainfall, 85% was from throughfall at the L. leptolepis stand, 84.5% at the thinned P. koraiensis stand, 83.2% at the unthinned P. koraiensu stand and 81.2% at the hardwood stand, showing greater throughfall at the conifer stand than at the hardwood stand. Stemflow showed 2.7% of rainfall at the hardwood stand, 1.3% at the unthinned P. koraiensis stand, 1.2% at the thinned P. koraiensis stand and 0.8% at the L. leptolepis stand, showing greater stemflow at the hardwood stand than at the conifer stand. Ion concentration of stemflow was greater than those of rainfall and throughfall. The conifer stand showed higher ion concentration than the hardwood stand both for cation and anion. The ion concentrations of throughfall and stemflow were higher in the descending order : $NH{_4}^+$-N > $K^+$ > $K^+$ > $Na^+$ > $Mg^{2+}$ for cations and $SO{_4}^{2-}$ > $NO{_3}^-$-N > $Cl^-$-N for anions. After the precipitation passed through the canopy, $K^+$ increased most at the hardwood stand, whereas $NH{_4}^+$-N did most at the P. koraiensis and L. leptolepis stands. The ion concentration of soil solution was higher in the descending order : $Ca^{2+}$ > $Mg^{2+}$ > $Na^+$ for cations and $NO{_3}^-$-N > $Cl^-$ > $SO{_4}^{2-}$ for anions. $NH{_4}^+$-N and $K^+$ seemed to be supplied primarily from atmospheric deposition while $Ca^{2+}$, $Mg^{2+}$ and $Na^+$ from weathering.

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Production of High purity $Mn_3O_4$Powder by Precipitation of Calcium fluoride in the Manganese Leaching Solution (망간침출액에서 불화칼슘화에 의한 高純度 망간酸化物의 製造)

  • 한기천;이계승;최재석;신강호;조동성
    • Resources Recycling
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    • v.11 no.1
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    • pp.3-8
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    • 2002
  • In order to make the high purity Mn$_3$O$_4$powder for the raw material of soft ferrite, Mn is extracted from the dust and the extracted solution is refined. The dust is generated in producing a medium-low carbon ferromanganese and contains 90% Mn$_3$O$_4$. Mn$_3$O$_4$in the dust was reduced into MnO by roasting with charcoal. Injection of the 180g/L of the reduced dust into 4N HCI solution increased pH of the leaching solution higher than 5 and then a ferric hydroxide was precipitated. Because the ferric hydroxide co-precipitates with Si ion etc, Fe and Si ion was removed from the solution and the about 10% Mn solution was obtained. The solution was diluted with water to Mn-15000 ppm and $NH_4$F was injected into the diluted solution at $70^{\circ}C$ to the F-3000 ppm. As a result, Ca ion is precipitated as $CaF_2$and the residual concentration of Ca was 14 ppm. Injection of the equivalent (NH$1.5M_4$)$_2$$CO_3$solution as 2 L/min at $25^{\circ}C$ into the above solution precipitated a fine and high purity $MnCO_3$powder. The deposition was filtrated and roasted at $1000^{\circ}C$ for 2 hours. As a result, $MnCO_3$powder is converted into $Mn_3$$O_4$powder and it had $8.2\mu$m of median size. The final production is above 99% $Mn_3$$O_4$powder and it satisfied the requirement of high purity $Mn_3$$O_4$powder for a raw material of soft ferrite.

The Study on the Ion Water Characteristics of Raw Water in the Domestic Natural Mineral Water (국내 유통 중인 먹는샘물 원수의 이온류 수질 특성에 관한 연구)

  • Lee, Leenae;Ahn, Kyunghee;Min, Byungdae;Yang, Mihee;Choi, Incheol;Chung, Hyenmi;Park, Juhyun
    • Journal of Korean Society on Water Environment
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    • v.32 no.5
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    • pp.442-449
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    • 2016
  • The goal of this study is to provide basic data to establish a foundation for the provision of safe drinkable water. The raw water of natural mineral water was analyzed to determine the quantities of anions (F-, Cl-, NO3-N-, and SO42- ) and cations (Ca2+, K+, Mg2+, and Na+) during the former and latter half of 2016. Analysis of the current quality of the raw water of natural mineral water among domestic manufacturers showed average anions contents of 0.46mg/L of fluorine, 8mg/L of chlorine ion, 1.5mg/L of nitrate nitrogen, and 12mg/L of sulfate ion. While the fluorine content was greater than the water quality criterion of 2.0mg/L at four points, the fluorine level was overall stable. The average cations contents included 21.3mg/L of calcium, 1.0mg/L of potassium, 3.4mg/L of magnesium, and 9.6mg/L of sodium. The chemical characteristics were compared among the major ions, and the results are presented in a piper diagram. The content ratio of cations was in the order of Ca2+> Na+>Mg2+>K+, whereas that of anions was in the order of SO42->Cl->NO3-N->F-. While the cations were slightly scattered, the anions were generally concentrated except for at a few points. The Ca-Na-HCO3 type was dominant overall in water sources from diorite, gneiss, and granite, while the Na-Mg-Ca-HCO3-Cl type was dominant in basalt sources. Mineral water manufacturers source their water under various conditions, including in-hole casing, excavation depth, and contact state of bedrock; even within the same rocky area, some differences in the water quality type can occur. When the depth of the water source was taken into account, the mean anions contents of F-, Cl-, NO3-N-, and SO42- were similar, with no significant differences according to depth. Of the cations, K+ and Na+ showed no significant differences across all the tubular wells, whereas Ca2+ and Mg2+ decreased in content with depth.

A Study on the Characteristics of Calcium Ion Separation by Adding Acidic/Basic Reagents (산/염기성 물질 주입에 따른 칼슘이온 분리 특성 연구)

  • Lee, Ye Hwan;Kim, Jeongeun;Kim, Sung Su
    • Applied Chemistry for Engineering
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    • v.31 no.1
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    • pp.103-107
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    • 2020
  • The purpose of this study is to resource calcium ions contained in most industrial by-products, and confirm the characteristics of calcium ions by extraction and separation conditions. Calcium oxide was used as a calcium extraction source, and hydrochloric acid as an extraction solvent, and the extraction amount according to the concentration of the extraction solvent and the pH dependent characteristics of the extract were analyzed. As the extractant concentration increased, the extracted amount increased while the pH for the extraction was kept constant. In order to separate extracted calcium ions, an acid-basic solution was injected and the formation of precipitates and also the form of precipitates were analyzed. When the sulfuric acid and sodium hydroxide solution of acid and basic substances were injected into the calcium extract, precipitates were formed and separated into CaSO4 and Ca(OH)2 forms.

Two Flavonoid-Based Compounds from Murraya paniculata as Novel Human Carbonic Anhydrase Isozyme II Inhibitors Detected by a Resazurin Yeast-Based Assay

  • Sangkaew, Anyaporn;Samritsakulchai, Nawara;Sanachai, Kamonpan;Rungrotmongkol, Thanyada;Chavasiri, Warinthorn;Yompakdee, Chulee
    • Journal of Microbiology and Biotechnology
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    • v.30 no.4
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    • pp.552-560
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    • 2020
  • Human carbonic anhydrase (CA) isozyme II has been used as protein target for disorder treatment including glaucoma. Current clinically used sulfonamide-based CA inhibitors can induce side effects, and so alternatives are required. This study aimed to investigate a natural CA inhibitor from Murraya paniculata. The previously developed yeast-based assay was used to screen 14 compounds isolated from M. paniculata and identified by NMR analysis for anti-human CA isozyme II (hCAII) activity. Cytotoxicity of the compounds was also tested using the same yeast-based assay but in a different cultivation condition. Two flavonoid candidate compounds, 5, 6, 7, 8, 3', 4', 5'-heptamethoxyflavone (4) and 3, 5, 7, 8, 3', 4', 5'-heptamethoxyflavone (9), showed potent inhibitory activity against hCAII with a minimal effective concentration of 10.8 and 21.5 μM, respectively, while they both exhibited no cytotoxic effect, even at the highest concentration tested (170 μM). The results from an in vitro esterase assay of the two candidates confirmed their hCAII inhibitory activity with IC50 values of 24.0 and 34.3 μM, respectively. To investigate the potential inhibition mechanism of compound 4, in silico molecular docking was performed using the FlexX and SwissDock software. This revealed that compound 4 coordinated with the Zn2+ ion in the hCAII active site through its methoxy oxygen at a distance of 1.60 Å (FlexX) or 2.29 Å (SwissDock). The interaction energy of compound 4 with hCAII was -13.36 kcal/mol. Thus, compound 4 is a potent novel flavonoid-based hCAII inhibitor and may be useful for further anti-CAII design and development.

Studies on the Production of Enzymes by Thermophilic Actinomycetes (PART II) Some Properties of $\alpha$-Amylase from Thermophilic Actinomycetes (고온성 방선균에 의한 순소생산에 관한 연구 (제2보) $\alpha$-Amylase의 효소학적 성질)

  • Yang, Han-Chul;Park, Yong-Jin;Cho, Hong-Yeon
    • Microbiology and Biotechnology Letters
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    • v.4 no.3
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    • pp.91-97
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    • 1976
  • During the course of studies on the production and utilization of thermostable ${\alpha}$-amylase from a thormophilic actinomycete species isolated from soil, partial characterization of the ${\alpha}$-amylase has been (arried out. The optimum pH for the dextrinogenic activity of the enzyme was found to be 6.5 and the maximum reaction rate was achieved at a temperature range of 55$^{\circ}$ to 65$^{\circ}C$. Calcium ion was recognized to have a slight effect in activating the enzyme, while heavy metal salts especially ferrous and cupric ions showed a remarkable inhibition effect. The enzyme was best protected iron thermal denaturation at pH 8.0 with tris-HCI buffer;inactivation was rapid at higher or lower pH values. Furthermore, its thermal stability was greatly increased by calcium ion, particulary at the final concentration of 1${\times}$10$\^$-2/ mole in the reaction mixture. The Km value for the ${\alpha}$-amylase was calculated to be 2.17${\times}$10$\^$-4/g per $m\ell$ and the energy of activation for the dextrinogenic reaction to be 12,000${\pm}$580 ㎈ per mole.

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Control of the CaCO3 Saturation Index Parameters for Protecting the Corrosion of Waterworks Pipe (상수도관 부식방지를 위한 탄산칼슘 포화지수(LI) 인자 제어에 관한 연구)

  • Park, Young-Bok;Kong, Sung-Ho
    • Applied Chemistry for Engineering
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    • v.16 no.3
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    • pp.372-378
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    • 2005
  • Calcium Carbonate Saturation Index (LI: Langelier Index), an indicator of $CaCO_3(s)$ saturation, indicates corrosiveness of drinking water and it has been used to monitor drinking water conditions in USA, E.U, and Japan. The objective of this research was to measure LI parameters including water temperature, pH, total alkalinity, calcium ion concentration, and electric conductivity, and to evaluate possibility of using LI in domestic system. Results showed that water temperature varied from 2.0 to $26^{\circ}C$ during 15 months, indicating an average annual temperature of $23.9^{\circ}C$. Total alkalinity was from 20 to 45 mg/L. The concentration difference between total alkalinity and $HCO_3{^-}$ value was hardly observed; the concentration of total alkalinity can be replaced by that of $HCO_3{^-}$. Tap water had a medium corrosiveness since LI values were from 2.0 to 0.5. To reduce the corrosiveness and to increase LI values of drinking water, the results of this study showed that chemicals such as $Ca(OH)_2$, $CaCO_3$, NaOH, or $NaHCO_3$ should be added to water treatment plants.