• Title/Summary/Keyword: Na-P zeolite

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A Study of the Utilization of Feldspathic Sand as a Fortified Functional Filtering Material for Water Purification (고 기능성 수질 정화 여과재로서의 장석질 모래 활용연구)

  • 고상모;송민섭;홍석정
    • Journal of the Mineralogical Society of Korea
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    • v.16 no.4
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    • pp.283-293
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    • 2003
  • Domestic water treatment plants operate the rapid and slow filtering system using the filtering sands. Most of them are composed of beach sands, which have less sorption capacity of heavy metals as well as organic contaminants. Therefore, the development of fortified functional filtering materials with high removal capacity of organic and inorganic contaminants is needed to prevent the unexpected load of contaminated source water. This study aims to test the hydrochemical change and the removing capacity of heavy metals such as Cd, Cu, and Pb on the Jumunjin sand, feldspathic sand(weathering product of Jecheon granite), feldspathic mixing sand I(feldspathic sand mixed with 10 wt% zeolite), and feldspathic mixing sand II (feldspathic sand mixed with 20 wt% zeolite). Feldspathic mixing sand I and II showed the eruption of higher amounts of cations and anions compared with the Jumunjin sand and feldspathic sand. They also showed higher eruption of Si, Ca, $SO_4$ ions than that of Al, $NO_3$, Fe, K, Mg, and P. Feldspathic mixing sand II caused higher eruption of some cations of Na, Ca, Al than feldspathic mixing sud I, which is the result controlled by the dissolution of zeolite. Jumunjin sand and feldspathic sand showed very weak sorption of Cd, Cu and Pb. In contrast to this, feldspathic mixing sand I and II showed the high sorption and removal capacity of the increasing order of Cd, Cu and Pb. Feldspathic mixing sand II including 20% zeolite showed a fortified removal capacity of some heavy metals. Therefore, feldspathic mixing sand mixed with some contents of zeolite could be used as the fortified filtering materials for the water filtering and purification in the domestic water treatment plants.

Adsorption Properties of U, Th, Ce and Eu by Myogi Bentonite Occurring in Japan (일본 묘기광산 벤토나이트의 물리화학적 성질 및 U, Th, Ce 및 Eu 흡착특성)

  • Song Min-Sub;Koh Sang-Mo;Kim Won-Sa
    • Journal of the Mineralogical Society of Korea
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    • v.18 no.3 s.45
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    • pp.183-194
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    • 2005
  • The mineralogical, physicochemical and thermal properties of the Myogi bentonite occurring in Japan were measured. A adsorption properties of U, Th, Ce and Eu ions on the Myogi bentonite were also investigated in different solution concentrations and pH conditions. The Myogi bentonite showed a strong alkaline character (pH 10.4), very high swelling, viscosity property and CEC, and a slow flocculation behavior due to the strong hydrophilic property. By the thermal analysis, the dehydroxylation of crystal water in bulk and clay fractions of the Myogi bentonite occur at $591^{\circ}C$ and $658^{\circ}C$, respectively, The adsorption experiments of ions such as U, Th, Ce and Eu were conducted for 0.2 g bentonites with 20mL solutions of various concentrations and different pH conditions with pH 3, 5, 7, 9, and 11. As a result, the Myogi bentonite showed excellent adsorption capacities for Ce, Th and Eu ions, whereas U ion showed very low adsorption capacity. Generally, Ce, Th and Eu ions showed the similar adsorption properties for the different concentrated solutions and pH conditions. These adsorption properties seem to be affected by the formation of various forms of chemical species and precipitation as well as ionic exchange reaction and surface adsorptions on smectite. Some associated zeolite minerals perhaps have some effects on the adsorption of U, Th, Ce and Eu on Myogi bentonite.

Synthesis of Single Crystalline Analcime and Its Single-crystal Structure, |Na0.94(H2O)|[Si2.06Al0.94O6]-ANA: Determination of Cation Sites, Water Positions, and Si/Al Ratios (결정성 아날심(|Na0.94(H2O)|[Si2.06Al0.94O6]-ANA)의 합성 및 단결정구조: 양이온 및 물 분자의 위치, Si/Al 비의 결정)

  • Seo, Sung-Man;Suh, Jeong-Min;Ko, Seong-Oon;Lim, Woo-Taik
    • Journal of the Korean Chemical Society
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    • v.55 no.4
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    • pp.570-574
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    • 2011
  • Large colorless single crystals of analcime with diameters up to 0.20 mm have been synthesized from gels with the composition of $3.00SiO_2$ : $1.50NaAlO_2$ : 8.02NaOH : $454H_2O$ : 5.00TEA. The fully $Na^+$-exchanged analcime have been prepared with aqueous 0.1 M NaCl (pH adjusted from 6 to 11 by dropwise addition of NaOH). The single-crystal structure of hydrated $|Na_{0.94}(H_2O)|[Si_{2.06}Al_{0.94}O_6]$-ANA per unit cell, a=13.703(3) ${\AA}$, has been determined by single-crystal X-ray diffraction technique in the orthorhombic space group Ibca at 294 K. The structure was refined using all intenties to the final error indices (using only the 1,446 reflections for which $F_o$ > $4{\sigma}(F_o))R_1/wR_2$ = 0.054/0.143. About 15 $Na^+$ ions are located at three nonequivalent positions and octahedrally coordinated. The chemical composition is $Na_{0.94}(H_2O)Si_{2.06}Al_{0.94}O_6$. The Si/Al ratio of synthetic analcime is 2.19 determined by the occupations of cations, 14.79, in the single-crystal determination work.

Evaluating Heavy Metal Stabilization Efficiency of Chemical Amendment in Agricultural Field: Field Experiment (안정화제 처리에 따른 중금속 오염 농경지 복원의 효율성 평가: 현장실증시험)

  • Oh, Se-Jin;Kim, Sung-Chul;Yoon, Hyun-Soo;Kim, Ha-Na;Kim, Tae-Hwan;Yeon, Kyu-Hun;Lee, Jin-Soo;Hong, Sung-Jo;Yang, Jae-E.
    • Korean Journal of Soil Science and Fertilizer
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    • v.44 no.6
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    • pp.1052-1062
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    • 2011
  • Residual of heavy metals originated from abandoned metal mines in agricultural field can cause adverse effect on ecosystem and eventually on human health. For this reason, remediation of heavy metal contaminated agriculture field is a critical issue. In this study, five different amendments, agriculture lime, dolomite, steel slag, zeolite, and compost, were evaluated for stabilization efficiency of heavy metals in agricultural field. Applied mixing ratio of amendments was varied (2% or 6%) depending on properties of amendments. Result showed that soil pH was increased compared to control (6.1-6.7) after mixing with amendments and ordered as dolomite (7.2~8.3) > steel slag (6.7~8.1) > agriculture lime (6.6~7.4) > zeolite (6.2~6.9) > compost (6.1~7.1). Among other amendments, agriculture lime, steel slag, and dolomite showed the highest stabilization efficiency of heavy metals in soil. For Cd, stabilization efficiency was 49~72%, 51~83%, and 0~36% for agriculture lime, steel slag, and dolomite respectively. In case of Pb, 43~64, 37~73%, and 51~73% of stabilization efficiency was observed for agriculture lime, steel slag, and dolomite respectively. However, minimal effect of heavy metal stabilization was observed for zeolite and compost. Based on result of this study, amendments that can increase the soil pH were the most efficient to stabilize heavy metal residuals and can be adapted for remediation purpose in agricultural field.

Adsorption and Activity Changes of Nitrofen by Clay Minerals (점토광물(粘土鑛物)에 의한 Nitrofen의 흡착(吸着) 및 활성(活性) 변화(變化))

  • Kim, Dong-Cheol;Choi, Jyung
    • Korean Journal of Environmental Agriculture
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    • v.5 no.1
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    • pp.67-72
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    • 1986
  • The nitrofen adsorption on several clay minerals was determined by sludge method to know the effect of clay minerals on the nitrofen activity. The bioassay was conducted with wheat seedlings to study the influence of the adsorbed nitrofen on the nitrofen activity. It is apparant that a four hours shaking was enough to reach the equilibrium concentration. The more the amount of sample, the more nitrofen was adsorbed by clay minerals, whereas the more nitrofen adsorption per unit gram of sample was observed at a 200 mg addition than a 400 mg in the same nitrofen solution. A little amount of nitrofen was adsorbed on Ca-zeolite or Ca-kaolinte, and much more nitrofen was adsorbed on Na-montmorillonite than the other clay minerals in the experiment. Little effect of pH on the adsorption would be attributed to physical adsorption between nitrofen molecule and clay surface. Na-and Ca-montmorillonite were the most effective in reducing the phytotoxicity of nitrofen to the growth of wheat seedlings among clay minerals which nitrofen was added to the growth media.

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Treatment of $NH_3-N$ in Drinking Water Using Ion Exchange (이온교환을 이용한 음용수의 $NH_3-N$ 처리)

  • Chae, Yong-Gon
    • Journal of environmental and Sanitary engineering
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    • v.23 no.1
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    • pp.67-72
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    • 2008
  • Ion exchange performance to remove Ammonium in water was studied using commercially available strong acidic cationic exchange resin of $Na^+$ type in the batch and continuous column reactors. The performance was tested using the effluent concentration histories for continuous column or equilibrium concentrations for batch reactor as a function of time until resins were exhausted or reached ionic equilibrium between resin and solution. The results shoed that cationic exchange resin used in this study was more effective than activated carbon or zeolite for ammonium removal. Ammonium removal with the ion exchange resin temperature to be high qualitative recording minuteness but increases about seasonal change of temperature was judged with the public law where the adaptability is excellent. When the pH comes to be high at 11 degree, the ammonium was not effectively removed.

The Gas Permeation Properties of Polyimide/Zeolite Membrane (폴리이미드/제올라이트 막의 기체투과 특성)

  • 최익창;김건중;남세종
    • Proceedings of the Membrane Society of Korea Conference
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    • 1998.04a
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    • pp.46-48
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    • 1998
  • 1. 서론 : 최근에 기체분리막의 재료로 많이 연구가 되고 있는 폴리이미드는 열, 화학적으로 안정하며 기계적 강도가 우수한 고분자재료이다. 그동안 본 연구실에서는 폴리이미드를 직접 합성하여 플라즈마처리, UV 처리등과 같은 고분자막수식에 의한 방법과, 무기재료와 폴리이미드를 이용하는 복합막 제조 등으로 폴리이미드의 투과특성을 향상시키는 연구를 진행해 왔다. 본 실험에서는 고분자재료로 폴리이미드 계열 중 가장 산소투과계수가 높은 6FDA-p-TeMPD 폴리이미드와 산소투과계수는 작고 선택도가 높은 6FDA-m-TeMPD 폴리이미드를 사용하였고, 무기재료는 surface pore size가 7.3${\AA}$, super cage가 13${\AA}$인 다공성 물질로 흡착력이 뛰어난 NaX형 제올라이트를 사용하였다. (생략)

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Sorption of Radioactive Cobalt and Ruthenium on Soil Minerals (방사성 코발트 및 루테늄의 토양 흡착)

  • Lee, Byung-Hun;Hands, J.D.
    • Journal of Radiation Protection and Research
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    • v.15 no.2
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    • pp.7-16
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    • 1990
  • The sorption of radioactive cobalt and ruthenium on alumina, silica gel, zeolite 3A, kaolin and Na-bentonite has been studied as a function of pH. nuclide concentration and ionic strength. Retardation factor for cobalt and ruthenium on soil minerals was determined through porosity measurement. Hydrolysed species, cobalt and ruthenium interact with solid surfaces by physical adsorption processes. Freundlich sorption isotherms for cobalt and ruthenium are effectively linear. The sorption decreases with increasing ionic strength for cobalt and ruthenium. The effect of increasing porosity on the retardation factor countered the effect of a significant increase in the distribution coefficient.

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Synthesis of Borosilicate Zeotypes by Steam-assisted Conversion Method (수증기 쪼임법에 의한 제올라이트형 보로실리케이트 제조방법)

  • Mansour, R.;Lafjah, M.;Djafri, F.;Bengueddach, A.
    • Journal of the Korean Chemical Society
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    • v.51 no.2
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    • pp.178-185
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    • 2007
  • Intermediate pentasil borosilicate zeolite-like materials have been crystallized by a novel method named steam-assisted conversion, which involves vapor-phase transport of water. Indeed, amorphous powders obtained by drying Na2O.SiO2.B2O3.TBA2O gels of various compositions using different boron sources are transformed into crystalline borosilicate zeolite belonging to pentasil family structure by contact with vapors of water under hydrothermal conditions. Using a variant of this method, a new material which has an intermediate structure of MFI/MEL in the ratio 90:10 was crystallized. The results show that steam and sufficiently high pH in the reacting hydrous solid are necessary for the crystallization to proceed. Characterization of the products shows some specific structural aspects which may have its unique catalytic properties. X-ray diffraction patterns of these microporous crystalline borosilicates are subjected to investigation, then, it is shown that the product structure has good crystallinity and is interpreted in terms of regular stacking of pentasil layers correlated by inversion centers (MFI structure) but interrupted by faults consisting of mirror-related layers (MEL structure). The products are also characterized by nitrogen adsorption at 77 K that shows higher microporous volume (0.160 cc/g) than that of pure MFI phase (0.119 cc/g). The obtained materials revealed high surface area (~600 m2/g). The infrared spectrum reveals the presence of an absorption band at 900.75 cm-1 indicating the incorporation of boron in tetrahedral sites in the silicate matrix of the crystalline phase.

Screening of Adsorbent to Reduce Salt Concentration in the Plastic Film House Soil under Continuous Vegetable Cultivation (시설채소재배지의 토양특성과 흡착제 종류별 염류경감 효과)

  • Ok, Yong-Sik;Yoo, Kyung-Yoal;Kim, Yoo-Bum;Chung, Doug-Young;Park, Yong-Ha;Yang, Jae-E.
    • Korean Journal of Environmental Agriculture
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    • v.24 no.3
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    • pp.253-260
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    • 2005
  • Salt accumulation in the plastic film house soils under continuous cultivation condition causes problems such as salt damages to plants, nitrate accumulation in vegetables, groundwater contamination, etc. due to excess application of fertilizers. Objective of this research was to find an optimum adsorbent to reduce salt concentration in the soil solution of plastic film house soils, where crop injuries have been observed due to the salt accumulation. The soils were significantly high in available P $(1,431{\sim}6,516mg\;kg^{-1}),\;NO_3-N\;(117.60{\sim}395.73mg\;kg^{-1})$, exchangeable Ca $(4.06{\sim}11.07\;cmol_c\;kg^{-1})$ and Mg $(2.59{\sim}18.76\;cmol_c\;kg^{-1})$, as compared to those of the average upland soils in Korea. Soils were treated with each of adsorbent such as ion-exchange resin, zeolite, rice bran, etc. at 2% level and prepared into saturated-paste samples. After equilibrium, soil solution was vacuum-extracted from the soil and measured for changes of the pH, EC, and concentrations of $Ca^{2+},\;Mg^{2+},\;K^+,\;Na^+,\;{NH_4}^+,\;{PO_4}^{3-}\;and\;{NO_3}^-$. Rice bran effectively removed ${PO_4}^{3-}\;and\;{NO_3}^-$ in the soil solution up to 100%. Efficiency was decreased in the orders of rice bran > ion-exchange resin > zeolite. Removal efficiencies of zeolite and ion-exchange resin for $Ca^{2+}$ were ranged from 1 to 65% and from 7 to 61%, respectively. Ion-exchange resin was also effective for removing $Mg^{2+},\;K^+,\;Na^+,\;and\;{NH_4}^+$. Overall results demonstrated that rice bran and ion-exchange resin could be applicable for salt accumulated soil to remove the respective anion and cation.