• Membrane Journal
• /
• v.18 no.3
• /
• pp.250-255
• /
• 2008

Zeolite A have been known to be chemically, mechanically and thermally quite stable. The ion-exchanged membranes were tested for the removal of water from ethanol/water mixtures by pervaporation. Since it is quite difficult to prepare the potassium form of zeolite A by a direct synthesis, it was obtained by the ion-exchange method from NaA zeolite. The effects of concentration of ethanol at the feed side and the temperature were studied on the permeation flux and the separation factor of water. After $Na^+$ ion was exchanged to $K^+$ ion, it was found that the total flux decreased and the separation factor increased.

• Journal of the Korean Chemical Society
• /
• v.36 no.3
• /
• pp.351-359
• /
• 1992

Interaction of xenon with alkaline-earth cations in Y zeolite supercage was studied by xenon adsorption and $^{129}Xe$ NMR experiments. The CaY and the BaY samples were prepared by exchanging $Ca^{2+}$ and $Ba^{2+}$ into a high-purity NaY zeolite. Xenon adsorption isotherms of these samples were obtained by using a conventional volummetric gas adsorption apparatus in the range of 260 to 320 K and the chemical shift in the $^{129}Xe$ NMR spectrum of the adsorbed xenon was measured at 296 K. The chemical shift against pressure was quantitatively explained assuming that the xenon gas exchanged very rapidly between various adsorption sites consisting of zeolite-framework surface and alkaline-earth ion. From this analysis, it was found that the alkaline-earth ion adsorbed xenon more strongly than $Na^+$ ion and zeolite-framework surface. Baring on the difference of the adsorption strength, the number of the alkaline-earth cations present in the zeolite supercage could be estimated by analyzing the adsorption isotherm.

• Journal of Environmental Health Sciences
• /
• v.33 no.4
• /
• pp.317-324
• /
• 2007

The sewage treatment sludge disposal has become a serious environmental problem because of restricted direct land-filling and oceandumping in spite of their large amounts discharged. So the recycling of sewage treatment sludge is very useful alternative for waste management. Here, we studied the feasibility of zeolite synthesis in open system from the sewage treatment sludge incinerator fly ash by means of hydrothermal synthesis. We considered the concentration of NaOH, reaction time, reaction temperature and reaction step as synthesis variables. The phase of zeolite products was identified by X-ray diffractometer(XRD) and ammonium ion exchange test was performed for the raw fly ash and two zeolite products(Z-3 and Z-5). In leaching test of the raw fly ash, hazard metal is detected very low level compared with regulatory leaching test standard. But in total recoverable test, the total contents of the fly ash were very high in terms of the standard for waste-derived fertilizer. Through hydrothermal reaction, small amount of zeolite P was synthesied in 1 N of NaOH solution and relatively large amount of hydroxysodalite was synthesied in 3 N and 5 N of NaOH solution with similar peak intensity. Addition of an aging step in the synthesis didn't increase the amount of zeolite phase. Maximum $NE_4^+-N$ exchange capacity is 1.49 mg $NH_4^+-N/g$ in Z-3 and 1.38 mg $NH_4^+-N/g$ in Z-5. Most of the ammonium ion is exchanged in 30 minutes and disorption did not occur until 5 hours.

• Economic and Environmental Geology
• /
• v.34 no.2
• /
• pp.167-173
• /
• 2001

Through alkaline hydrothermal activation processes, Na-A type zeolite was synthesized as a single phase with funnel-glass waste from a television tube factory. The autoclaving was performed in a closed teflon vessel in the range of 80~95$^{\circ}$C. The silica-rich solution as a starting material was hydrothermally synthesized with quartz in IN NaOH by heating 350uC under the pressure of 1,500 atm. $NaAlO_2$ was made from NaOH and Al(OHh by heating 95$^{\circ}$C for 2-3 hours and the molar ratios of it were $Na_2O/Al_2O_3$ = 1.4 and $H_2O/Na_2O$=8. The equi-dimensional A type zeolite (1-2 11) was formed by the simple mixing of the silica-rich solution, glass waste and $NaAlO_23$ for 1-3 hours-heating at $80^{\circ}C$. The characterization of the reaction product shows Na-A as a single phase. The synthesized zeolite has cuba-dodecahedral form and $Ca^{2+}$ ion exchange capacity of the Na-A was in the range of 215-220 mequiva1entilOO g.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2001.04a
• /
• pp.7-10
• /
• 2001

Adsorption of the pesticides (phosphamidon, fenitrothion, triadimefon and diniconazole) in natural zeolite (CL $I_{N}$) and several synthetic zeolites was incestigated. The pesticides were not adsorbed on zeolites (Na-Pl, SOD, ANA, JBW and CAN) synthesized from Jeju scoria. The distribution coefficient ( $K_{D}$) and the Freundlich constant ( $K_{F}$) decreased in the following sequences. FC $C_{W}$ (waste catalytic cracking catalyst)>FA $U_{F}$ (FAU Synthesized from coal fly ash)>(FAU+Na-Pl)$_{SF}$ (the mixture of FAU and Na-Pl synthesized from the ratio of Jeju scoria 6 to coal fly ash 4 by weight)>CL $I_{N}$ among the zeolites; diniconazole>fenitrothion> triadimefon>phosphamidon. As the temperature was increased, the amount of pesticide adsorbed per unit mass of zeolite increased for FC $C_{W}$, FA $U_{F}$ and (FAU+Na-Pl)$_{SF}$ but it decreased for CL $I_{N}$, for all the pesticides used in this study. It was independent of pH for phosphamidon, fenitrothion and triadimefon, but decresed as pH was increased for all the zeolites used in this study.y.udy.y.y.y.y.y.y.

• Korean Journal of Soil Science and Fertilizer
• /
• v.29 no.2
• /
• pp.130-136
• /
• 1996

This study was carried out easily to determine the refreshing time of natural Zeolite used for the clearing of Livestock waste water and to investigate the relationship between EC of solution and adsorption amount on Zeolite. During the adsorption reaction, EC of supernatant solution decreased till the equilibrium was reached and kept a constant level after it. EC was greatly decreased with the concentration of solution and the magnitude of adsorbent. Decrease in EC of suspension was found to be lesser in addition of Na-Zeolite than Ca-Zeolite. EC change of Livestock waste water was shown to be similar tendency to that of the simulated waste water. On the cumulative adsorption isotherm, the EC of suspension increased until the EC value of the initial solution as the increase in treatment times. Therefore, it is apparent that the exchange point of natural zeolite should be in the vicinity of the EC value of initial waste water.

• Journal of Korean Society of Environmental Engineers
• /
• v.37 no.3
• /
• pp.145-151
• /
• 2015

In order to remove Sr ions and Cs ions from aqueous solution, PS-zeolite beads were prepared by immobilizing zeolite with polysulfone (PS). The prepared PS-zeolite beads were characterized by SEM, XRD, FT-IR, and TGA. The optimum condition to prepare PS-zeolite beads was 1.25 g of PS content and 2 g of zeolite A. The removal efficiencies of Sr and Cs ions by the PS-zeolite beads increased as the solution pH increases and nearly reached a plateau at pH 4. The PS-zeolite beads prepared in this study showed a remarkably high selectivity for Sr ion and Cs ion under the coexistence of ions such as $Na^+$, $K^+$, $Mg^{2+}$, and $Ca^{2+}$. Zeolite particles detached from the PS-zeolite beads were not observed on this experiments, and also the PS-zeolite beads maintained the morphological structure on a SEM image. The removal efficiencies of Sr ions and Cs ions by PS-zeolite beads were maintained over 90% even after five adsorption-desorption cycles. These results implied that the prepared PS-zeolite beads could be an available adsorbent for the adsorption of Sr and Cs ions. These results suggest that the PS-zeolite can potentially be used as an adsorbent in radioactive ions removal for the treatment of industrial wastewater.

• Korean Journal of Environmental Agriculture
• /
• v.10 no.1
• /
• pp.11-19
• /
• 1991

This study was carried out to develop the low-priced adsorbent by synthesizing the zeolite of high CEC with the natural zeolite and examining the ability of this zeolite to adsorb heavy metals. The dominant clay minerals were clinoptilolite and mordenite in natural zeolite, while phillipsite in the synthesized zeolite. Adsorption reaction of Cu and Zn on clays were reached to equilibrium after 1 hr. The amount of adsorption was increased as the concentrations of heavy metals or the initial pH of suspension was increased. The synthesized zeolite adsorbed heavy metals about twice as much as the natural zeolite. The adsorption of heavy metals on the synthesized zeolite was less affected by the initial pH of suspension than that on natural zeolite. At cumulative adsorption, the synthesized zeolite adsorbed much more heavy metals at early three treatments than the natural zeolite did. The amount of desorption by chloride salts was increased as the concentration of chloride salts was increased. The ability of salt to desorb was in the order of NaCl>$CaC1_2$>$AlC1_3$. It is estimated that the ability of the synthesized zeolite to remove heavy metals was better than that of the natural zeolite.

• Journal of Environmental Science International
• /
• v.10 no.6
• /
• pp.451-459
• /
• 2001

Adsorption characteristics of triadimefon and diniconazole(pesticide) by natural zeolite($CLI_N$) and several synthetic zeolites were Investigated. The synthetic zeolites used En this study were as follows: Faujasite synthesized from coal fly ash($FAU_F$); Zeolite synthesized from the mixture of FAU and Na-Pl synthesized from the ratio of Cheju scoria 6 to coal fly ash 4 by weight($(FAU + Na-Pl)_{SF}$); waste fluid catalytic cracking catalyst($FCC_W$). The distribution coefficient, $K_D$ and Freundlich constant, $K_F$ decreased in the fellowing sequence : $FCC_W ＞ FAU_F ＞ (FAU + Na-Pl)_{SF} ＞CLI_N$ among the zeolites. The distribution coefficient and the adsorption capacity of $(FAU + Na-Pl)_{SF}$ for pesticides were 4.4 and 2.6 times higher for triamefon, and 2.0 and 2.4 times higher for diniconazole than those of $CLI_N$, respectively.

• Economic and Environmental Geology
• /
• v.32 no.6
• /
• pp.575-584
• /
• 1999

Through alkaline hydrothermal activation processes, zeolite minerals were synthesized from fly ashes produced at Youngwol and Boryoung power plants. The syntheses were performed in a closed teflon vessel with a teflon-coated magnetic bar for continuous stirring during the reaction periods. The experiments were caeeied out at three different reaction temperatures ($100^{\circ}C$,$200^{\circ}C$, and $250^{\circ}C$), with varying NaOH concentations (0.5~8N) and reaction time (24 to 288 hours). Mineralogical characterization of the reaction products indicated that Na-p1, analcime, and hydroxysodalite were dominant zeolites formed from the both fly ashes at the given experimental conditions, The highest amount of zoelites produced from the Youngwol and Boryoung fly ash were:60 and 45wt%for Na-P1, 70 and 45wt% for analicime, 50 and 40wt% for hydroxysodalite, respectively. A small amount of zeolite A was present in NaP-dominant dample is about 250 meq/100g. This suggests the possibility of its utilization as an ion-absorbent.