• Title/Summary/Keyword: Natural zeolites

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Removal of $Cs^+$ and $Sr^{2+}$ Ions by Natural Zeolites (천연 제올라이트를 이용한 $Cs^+$$Sr^{2+}$ 이온의 제거)

  • 김덕수;박재우
    • Journal of Environmental Science International
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    • v.2 no.4
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    • pp.347-356
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    • 1993
  • The three natural zeolites collected in Yungil-gun, Kyungsangbuk-do, Korea, were analyzed by means of chemical wet methods and X-ray diffraction. The results indicated that the primary species of those zeolites were clinoptilolite mixed with heulandite, feldspar, montmorillonite, and quartz. These zeolites were chemically treated with NaOH, $\textrm{Ca(OH)}_2$, and HCl solution and their differences were also studied with X-ray diffraction method. The capabilities of removing $Cs^+$ and Sr^{2+}$ ions with chemically untreated zeolites, chemically treated zeolites, and also with synthetic zeolites were compared. The effect of other cations in removing Sr^{2+}$ ions was also studied. The experimental results showed that$Cs^+$ and Sr^{2+}$ ions could be removed up to 98% and 95% respectively out of 5 ppm with chemically untrearted natural zeolites. The treatment of 0.02N-$\textrm{Ca(OH)}_2$ and that of 2N-NaOH were most effective In removing $Cs^+$ and Sr^{2+}$ ions, respectively. It was found that the mountaintop of Sangjung 1-dong natural zeolite treated with 2N-NaOH was most efficient in removing Sr^{2+}$ ions mixed with other cations, compared with any other chemically treated and untreated natural zeolites in this work.

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Comparions of Removal Performances of Divalent Heavy Metals by Natural and Pretreated Zeolites (천연 및 전처리 제올라이트에 의한 2가 중금속 이온 제거능의 비교.검토)

  • 감상규;김덕수;이민규
    • Journal of Environmental Science International
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    • v.8 no.3
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    • pp.399-409
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    • 1999
  • The three domestic natural zeolites(Yong dong-ri (Y), Daesin-ri (D), Seogdong-ri (S)) harvested in Kyeongju-shi and Pohang-shi, Kyungsangbug-Do, were pretreatd with each of the NaOH, $Ca(OH)_2$ and NaOH following HCl solutions, and the removal performances of divalent haevy metals(Cu, Mn, Pb, and Sr) for natural and pretreated zeolites were investigated and compared in the single and mixed solutions. The natural zeolite-heavy metal system attained the final equilibrium plateau within 20 min, irrespective of initial heavy metal concentration. The heavy metal uptakes increased with increasing initial heavy metal concentration and pH. The heavy metal uptakes for natural zeolites decreased in the following sequences : D>Y>S among the natural zeolites; Pb>Cu>Sr>Mn among the heavy metals. The pretreated zeolites showed higher heavy metal removal performances than natural zeolites and decreased in the order of NaOH, NaOH following HCl, $Ca(OH)_2$ treatment among the pretreatment methods. The heavy metal ion exchange capacity by natural and pretreated zeolites was described either by Freundlich equation or Langmuir equation, but it followed the former better than the latter. The heavy metal uptakes for natural zeolites decreased in the mixed solution, in comparing with those in the single solution and especially, the manganese uptake decreased greatly in the mixed solution. The pretreated zeolites showed the improved removal performances of heavy metals in the mixed solution than in the single solution and the heavy metal uptakes by those in the mixed solution showed the same trends in the single solution among the chemical treatment methods and heavy metals.

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Nitrogen Removal using Zeolite at On-site Wastewater Treatment System (소규모 오수처리 시스템에서의 제올라이트에 의한 질소 제거)

  • 방천희;권순국
    • Magazine of the Korean Society of Agricultural Engineers
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    • v.44 no.2
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    • pp.161-173
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    • 2002
  • Recently, absorbent biofilters, which are inexpensive and easy to manacle, have been supplied to the rural areas, but have limitations in removing the nutrients effectively. Accordingly, as an alternative plan. natural zeolites were arranged in front or at the rear of the absorbent biofilters, and their removal efficiency for nitrogen and, ultimately, their applicability to the on-site wastewater treatment system were studied. Furthermore, the same experiments were carried out on artificial zeolites, made from coal ashes at National Honam Agricultural Experiment Station, to compare natural zeolites with artificial ones. Treated wastewater through the Absorbent Biofilter showed 22.6% nitrogen removal efficiency, while 64.6% was attained when natural Zeolites were placed in front of the absorbent biofilters (Zeolite-Aerobic process). As an addition, phosphorus was also efficiently removed. On the other hand, Aerobic-Zeolite process, which arranged natural zeolites at the rear of the biofilters, did not have significantly higher nitrogen removal as compared to the treatment using only the absorbent biofilters. Furthermore, upon regeneration of the natural zeolite, the ion exchange rate was fecund to increase over 10% as compared to before regeneration. Our results show that natural zeolites, applied to the on-site wastewater treatment system through the Zeolite-Aerobic process, not only increase the removal efficiency of nutrients, but, by choosing the appropriate regeneration time, can also be cast-effective. Artificial zeolites, on the other hand, though more efficient in removing nutrients, cannot be regenerated and, therefore, are not cost-effective.

Metal-Modified Natural Zeolite for Bacterial Media (미생물 담체 성능 향상을 위한 금속 치환)

  • Kim, Jae-Keun;Min, Jee-Eun;Park, Jae-Woo
    • 한국방재학회:학술대회논문집
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    • 2008.02a
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    • pp.811-813
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    • 2008
  • To see the effect of magnesium on adhesion to natural zeolites, a series of batch tests were performed in this research. Mixed bacteria were sampled from the digestion tank at a local sewage treatment plant in Seoul. Magnesium-zeolites were synthesized by mixing natural zeolites with 0.096 M, 0.24 M, and 0.48 M of MgCl2 solution. For comparison, manganese and trivalent ferric zeolites were also prepared. Two grams of 0.2 mm $\sim$ 0.3 mm sized zeolites(non-treated, Mg, Mn and Fe(III) treated zeolites) and 20 mL of water were mixed in a Corex 25 mL tube. Five milliliters of culture solution including bacteria was added to the tube. The tubes were equilibrated in a shaking incubator at mesophilic temperature $(30{\pm}2^{\circ}C)$. The bacterial concentrations were measured with a Microluminometer (New Horizons 3550i) and total organic carbon (TOC) spectrophotometer (Multi NC-3100).

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Reduction of cement consumption by producing smart green concretes with natural zeolites

  • Trung, Nguyen Thoi;Alemi, Nima;Haido, James H.;Shariati, Mahdi;Baradaran, Seyedata;Yousif, Salim T.
    • Smart Structures and Systems
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    • v.24 no.3
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    • pp.415-425
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    • 2019
  • This study was carried out to evaluate the natural zeolite in producing green concrete as an effort to prevent global warming and environmental impact problems of cement industries. To achieve this target, two types of natural zeolites applied to study physical, chemical and compressive strength of concrete containing different percentages of zeolites. The results in comparison with control samples indicate that compressive strength of zeolites mixes increases with the 15% replacement of zeolite instead of cement in all types of samples. In the water-cement ratio of 0.6, results showed an increase in the compressive strength of all percentages of replacement. This results indicate that using natural zeolites could be produced a green concrete by a huge reduction and saving in the consumption of cement.

Removal Characteristics of Strontium and Cesium tons by Zeolite Synthesized from Fly Ash (석탄회로 합성한 제올라이트에 의한 Sr(II) 및 Cs(I) 이온의 제거 특성)

  • 감상규;이동환;문명준;이민규
    • Journal of Environmental Science International
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    • v.12 no.10
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    • pp.1061-1069
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    • 2003
  • The adsorption behaviors of strontium and cesium ions on fly ash, natural zeolites, and zeolites synthesized from fly ash were investigated. The zeolites synthesized from fly ash had greater adsorption capabilities for strontium and cesium ions than the original fly ash and natural zeolites. The maximum adsorption capacity of synthetic zeolite for strontium and cesium ions was 100 and 154 mg/g, respectively, It was found that the Freundlich isotherm model could fit the adsorption isotherm. The distribution coefficients (K$\_$d/) for strontium and cesium ions were also calculated from the adsorption isotherm data, The distribution coefficients decreased with increasing equilibrium concentration of strontium and cesium ions in solution. By studying the removal of cesium and strontium ions in the presence of calcium, magnesium, sodium, potassium, sulfate, nitrate, nitrite, and EDTA (in the range of 0.01 - 5 mM) it was found that these coexistence ions competed for the same adsorption sites with strontium and cesium ions.

Adsorption Characteristics of Pesticides in Zeolites

  • Chang-Han Lee;Kil-Seong Kim;Sang-Kyu Kam
    • Journal of Environmental Science International
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    • v.31 no.12
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    • pp.1103-1115
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    • 2022
  • The adsorption characteristics of four pesticides (phosphamidon, fenitrothion, triadimefon, and diniconazole) on natural clinoptilolite (CLIN) and three synthetic zeolites were investigated. The synthetic zeolites included faujasite (FAUF) synthesized from coal fly ash; the mixture of FAU and Na-P1 (FAU + Na-P1)SF synthesized using Jeju scoria and coal fly ash at the ratio of 1.5 by weight; and waste fluid catalytic cracking catalyst (FCCW). The distribution coefficient, KD and the Freundlich constant, KF decreased in the following sequence: FCCW > FAUF > (FAU + Na-P1)SF > CLIN among the zeolites and diniconazole>fenitrothion> triadimefon> phosphamidon among the pesticides. The pesticide adsorptivity increased with increasing temperature for FAUF, (FAU+Na-P1)SF and FCCW, however, it decreased for CLIN, regardless of the type of pesticide. The adsorptivity of pesticides was independent of pH for phosphamidon, fenitrothion and triadimefon, whereas it decreased with increasing pH for diniconazole, regardless of zeolite type.

Natural Zeolities (제오라이트 광물(鑛物))

  • Sang, Ki Nam
    • Economic and Environmental Geology
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    • v.9 no.3
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    • pp.165-168
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    • 1976
  • Zeolites are aluminosilicates with a three dimensional framework structure enclosing pores occupied by cation and water molecules, both of which have considerable freedom of movement within certain limits. The ability of zeolites to exchange cation is one of the mere useful of their characteristics. The ion exchange condition of zeolites strongly affects absorption as well as other properties. The application, techniques of identification and evaluation of clinoptilolite, chabazite, mordenite and phillipsite are reviewed.

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The Effect of Na+-Ca2+ Ion-exchange for Heulandite on the Thermal Stability (Na+-Ca2+ 양이온 교환이 Heulandite의 열적 안정성에 미치는 영향)

  • Kim, Wha-Jung;Lee, Jae-Ik
    • Applied Chemistry for Engineering
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    • v.4 no.3
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    • pp.488-496
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    • 1993
  • Natural zeolites have recently been the subject of intensive research due to their versatilities in possible industrial applications. Among several different types of domestic natural zeolites, clinoptilolite, is one of the highly prospective domestic natural zeolites. However, it is always possible for heulandite, the isostructure of clinoptilolite, to coexist with clinoptilolite. Unfortunately, heulandite is thermally very unstable restricting its application to industrial process. In this paper, the effects of ion exchanges and heat-treatments on the thermal stability for domestic natural zeolite, heulandite are described. Two different ion-exchanging experiments were carried out followed by heat-treatments at different temperatures. X-ray, IR and AA spectroscopic analyses showed the enhancements in thermal stabilities of heulandite by $Na^+$ cation exchanges.

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Liquid Phase Adsorption Properties of Organo Surfur Compounds on Cation Exchanged Natural Zeolites (陽이온 交換한 天然 제올라이트에 依한 有機黃化合物의 液相吸着 特性)

  • Kim, Jong-Taik;Heo, Nam-Ho
    • Journal of the Korean Chemical Society
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    • v.28 no.3
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    • pp.194-202
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    • 1984
  • The adsorption properties of organo sulfur compounds on cation exchanged natural zeolites from n-heptane were investigated. The equilibrium adsorbed amounts were dependent upon the exchanged cation and the nature of organo sulfur compounds such as length, volume, electronical structure. The increasing orders of equilibrium adsorbed amounts were thiophene derivatives, disulfide, sulfide mercaptane and thiophene, benzothiaphene, dibenzothiophene. And $Co^{+2}$-zeolite was the most prominent adsorbant. Rate determining step of the adsorption at initial stage was intraparticle diffusion into the transitional pores of zeolite. These adsorption rates were dependent upon the bulkiness of adsorbate. Finally, preadsorbed water didn't affect these adsorption until the cation exchanged natural zeolite contained 2.26${\times}10^{-3}$ mol/g of water. It indicated that water preferentially occupied the micro pores of the cation exchanged natural zeolites.

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