• Current Research on Agriculture and Life Sciences
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• v.8
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• pp.29-34
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• 1990

This study was conducted to examine the influence of heat treatment on the $NH_4{^+}$ adsorption by zeolite and to determine the $NH_4{^+}$ loss from $NH_4-$ zeolite during the incubation. The dominant clay minerals of zeolite were clinoptiloiite and mordenite. $NH_4{^+}$ adsorption by zeolite was equilibrated at a 4hrs-shaking. The content of exchangeable $K^+$ of zeolite was increased with increase in the temperature of heat treatment but the amount of $NH_4{^+}$ adsorbed by zeolite was decreased. The amount of $NH_4{^+}$ in the soil treated with ammonium sulfate was decreased during incubation under the submerged condition but the amount of $NH_4{^+}$ adsorbed by zeolite was not decreased in the same course of incubation. It was estimated that $NH_4{^+}$ adsorbed by zeolite was resistant to $NH_4{^+}$-N loss by various reactions.

• Journal of the Korean Chemical Society
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• v.32 no.3
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• pp.171-178
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• 1988

The potential energy of adsorbate molecules in the main channel of $K^+$ ion exchanged zeolite L(K-L) was calculated. In K-L which adsorbs three molecules per unit cell, the interaction energies of $H_2O,\;NH_3,\;CH_3NH_2,\;(CH_3)_2NH,\;and\;(CH_3)_3N$ molecules with zeolite lattice are 61.11, 62.31, 65.68, 74.65, and 79.88kJ/mol, respectively. These values are less by 3.7∼12.6kJ/mol than $K^+$ ion affinities with adsorbing molecules. These results may be due to the facts that the electrostatic energies are reduced by the negative charge of the lattice oxygens. The distribution of adsorption sites of $NH_3$ and $CH_3NH_2$ in K-L was investigated by a technique of temperature programmed desorption. The experimental value of desorption energies of $NH_3$ and $CH_3NH_2$ on K-L are in good agreement with the theoritical values. It is concluded that the desorption of $NH_3$ and $CH_3NH_2$ on K-L is the first-order desorption with free readsorption.

• Journal of Bio-Environment Control
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• v.10 no.1
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• pp.50-54
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• 2001

Effect of NO$_3$:NH$_4$ratio and pH of nutrient solution on nitrate content of leaves was investigated for leaf lettuce(Lactuca sativa L.) grown by a deep flow technique. Ratios(in me.L$^{-1}$ ) of NO$_3$:NH$_4$tested were 12:1, 10:3 and 8:5. The treatment of 8:5 NO$_3$:NH$_4$ratio had two solutions, one with uncontrolled pH and the other with automatically controlled pH. Solution pH continuously increased in 12:1 NO$_3$:NH$_4$treatment. Solution pH decreased gradually more as NH$_4$ratio increased. Treatment of 8:5 NO$_3$:NH$_4$with automatic pH control satisfactorily maintained the solution pH in the range of pH 5.5-6.0. Nitrate content in leaves was the greatest in treatment of 12:1 NO$_3$:NH$_4$ and the least in treatment of 8:5 NO$_3$:NH$_4$with automatic pH control. Fresh weight decreased in treatments of 10:3 and 8:5 NO$_3$:NH$_4$, whereas it increased in treatments of 12:1 and 8:5 NO$_3$:NH$_4$with pH control. It was concluded that the growth and leaf nitrate content were the greatest in high NH$_4$treatment with automatic pH control.

• Applied Chemistry for Engineering
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• v.30 no.1
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• pp.122-131
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• 2019

In order to reuse and concentrate the sewage, a forward osmosis using fertilizer as draw solution was applied. Sewage-1, which is the supernatant after settling for 30 minutes for the primary settling basin influent, and Sewage-2, which is the supernatant after settling for 30 minutes for the effluent, and Sewage-3, which is the filtrate filtered through a $1{\mu}m$ cartridge filter for the effluent were tested. Eight draw solutions of $NH_4H_2PO_4$, KCl, $KNO_3$, $NH_4Cl$, $(NH_4)_2HPO_4$, $NH_4NO_3$, $NH_4HCO_3$, and $KHCO_3$ were used in consideration of osmotic pressure, solubility and pH. In the case of Sewage-3, the permeate flux was almost similar to that of the discharge water of the sewage treatment plant, and was larger than that of Sewage-1 and Sewage-2. $NH_4H_2PO_4$ was the smallest, and $NH_4NO_3$ was the largest in the specific reverse solute flux. $NH_4H_2PO_4$ was found to be most useful for the reuse and concentration of sewage because it contains nitrogen and phosphorus, which are the major components of fertilizer, as well as low specific reverse solute flux. When $NH_4H_2PO_4$ was used as the draw solution, the concentration factor after 24 hours for Sewage-3 was 1.72.

• Journal of Korean Society for Atmospheric Environment
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• v.33 no.6
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• pp.605-615
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• 2017

Efficient simultaneous reduction conditions for $NO_x$ and $NH_3$-slip was investigated in SCR (Selective Catalytic Reduction) process with load variation by applying dual catalysts (SCR catalyst, $NH_3$ decomposition catalyst) system. $N_2O$ formation characteristics were analyzed to look into possible undesirable reaction pathways. In the experiments of catalyst characteristics, various operational variables were tested for the combined catalytic system, such as $NH_3/NO_x$ ratio, temperature, oxygen concentration and $H_2O$. The reaction characteristics of $NO_x$, $NH_3$ and $N_2O$ were analyzed and optimal conditions could be evaluated for the combustion facility with varied load. In terms of $NO_x/NH_3$ simultaneous reduction and $N_2O$ formation suppression, optimal condition was considered NSR 1.2 and temperature $300^{\circ}C$. At this operational condition, $NO_x$ conversion was 98%, $NH_3$ reduction efficiency was 95%, generated $N_2O$ concentration 9.5 ppm with inlet $NO_x$ concentration of 100 ppm. In $NH_3-SCR$ process with $NH_3$ decomposition catalyst, $NO_x$ and $NH_3$ can be considered to be reduced simultaneously at limited conditions. The results of this study may be utilized as basic data at facilities requiring simultaneous $NO_x$ and $NH_3$ reduction for facilities with load variation.

• Korean Journal of Agricultural Science
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• v.46 no.4
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• pp.907-914
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• 2019

Ammonia (NH₃) that reacts with nitric or sulfuric acid in the air is the major culprit contributing to the formation of fine particulate matter (PM_2.5). NH₃ volatilization mainly originates from nitrogen fertilizer and livestock manure applied to arable soil. Cation exchange capacity (CEC) of peat moss (PM) and zeolite (ZL) is high enough to adsorb ammonium (NH₄⁺) in soil. Therefore, they might inhibit volatilization of NH₃. The objective of this study was to compare the effect of PM and ZL on NH₃ volatilization from upland soil. For this, a laboratory experiment was carried out, and NH₃ volatilization from the soil was monitored for 12 days. PM and ZL were added at the rate of 0, 1, 2, and 4% (wt wt^-1) with 354 N g m^-2 of urea. Cumulative NH₃-N volatilization decreased with increasing addition rate of both materials. Mean value of cumulative NH₃-N volatilization across application rate with PM was lower than that with ZL. CEC increased with increasing addition rate of both materials. While the soil pH increased with ZL, it decreased with PM. Increase in CEC resulted in NH₄⁺ adsorption on the negative charge of the external surface of both materials. In addition, decrease in soil pH hinders the conversion of NH₄⁺ to NH₃. Based on the above results, the addition of PM or ZL could be an optimum management to reduce NH₃ volatilization from the soil. However, PM was more effective in decreasing NH₃ volatilization than ZL due to the combined effect of CEC and pH.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2008.11a
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• pp.517-521
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• 2008

Struvite의 최적 생성조건은 NH$_4$-N의 초기농도에 관계없이 모두 NH$_4^+$, PO$_4^{3-}$ 및 Mg$^{2+}$가 등몰비이고 pH 10.5이었다. Struvite 침전반응에서 NH$_4$-N 및 PO$_4$-P 제거율에 미치는 struvite seeding 효과는 습윤상태의 struvite를 seeding할 경우 그 효과가 거의 없었으나 건조된 struvite를 seeding할 경우 NH$_4$-N의 제거율은 증가되지만 PO$_4$-P의 제거율은 감소되는 경향을 나타냈다. 이는 건조과정에서 struvite의 NH$_4$-N가 휘산되어 소실되었기 때문이다. Mg와 P원으로서 struvite의 재이용을 위한 적정 건조온도는 100$^{\circ}C$ 이하였으며 그 이상 온도에서는 struvite가 $NH_4MgPO_4\cdot6H_2O$형에서 MgPO$_4$형으로 상전이점에 따라 struvite seeding에 의한 NE$_4$-N의 제거율이 현저히 감소되었다. 건조된 struvite는 초기 NH$_4$-N의 몰농도 대비 50%를 seeding할 경우 60% 이상의 NH$_4$-N를 제거하였으며, seeding량을 150%로 증가시킬 경우 90% 이상의 NH$_4$-N 제거율을 얻을 수 있었다. 그러나 struvite를 반복 재사용할 경우 재사용 횟수에 비례하여 NH$_4$-N의 제거율은 감소하는 경향을 보여 재사용 횟수가 제한적임을 알 수 있었다.

• Journal of Applied Biological Chemistry
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• v.42 no.1
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• pp.25-28
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• 1999

For investigating the effectiveness of Korean natural zeolite for removal of $NH_4{^+}$ in waste waters containing $NH_4{^+}$ and $Cu^{2+}$, the adsorption of $NH_4{^+}$ and $Cu^{2+}$ by three Korean natural zeolite samples, which contained mordenite and/or clinoptilolite, was measured by adding solutions containing $NH_4{^+}$ and $Cu^{2+}$ or both at a concentration range from 1 to 7 mmol(+)/L of each cation. In the solutions, the zeolite samples adsorbed more amounts of $NH_4{^+}$ than $Cu^{2+}$. By seven successive equilibrations, Korean natural zeolites adsorbed $NH_4{^+}$ corresponding to 23~33% of those cation exchange capacity from the solution containing both $NH_4{^+}$ and $Cu^{2+}$ at 3 mmol(+)/L of each cation. Whereas, the corresponding adsorption of $Cu^{2+}$ was 17-27% of the CEC. Korean natural zeolite exhibited selectivity for $NH_4{^+}$ but not for $Cu^{2+}$. Nevertheless, it using as a soil amendment after removing of $NH_4{^+}$ in waste waters should be carefully controlled on the application rate.

• Proceedings of the KSME Conference
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• 2008.11b
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• pp.3096-3101
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• 2008

Selective Catalytic Reduction (SCR) technology is well-known to be effective for the reduction of NOx emission. So car manufacturers has adopted Ures-SCR system to be satisfied with emission regulation. This paper discusses the effective of $NH_3/NOx$ ratio and SCR catalyst temperature in the $NH_3$-SCR reactor on DeNOx performance. So it is shown the characteristic of NOx conversion and ammonia slip using the $NH_3$ instead of Urea-Solution. From the result of this study, it is found to optimize $NH_3/NOx$ ratio to have the best case of high NOx conversion and low ammonia slip at variable SCR catalyst temperatures. Lastly, it is also found the characteristics of NOx conversion and ammonia slip with compared with Urea.

• Journal of the Korean Magnetic Resonance Society
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• v.21 no.2
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• pp.67-71
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• 2017

At high temperature, the roles of $NH_4$ and $H_2O$ in $(NH_4)_2Fe(SO_4)_2{\cdot}6H_2O$ and $(NH_4)_2Zn(SO_4)_2{\cdot}6H_2O$ single crystals were investigated using a pulse NMR spectrometer. Temperature was shown to have a significant influence, causing changes in the deformation of $NH_4$ and $H_2O$. From the $^1H$ NMR and $^{14}N$ NMR spectrum, the forms of environment surrounding $^{14}N$ in $NH_4$ groups is more important than the loss of $H_2O$ groups. NMR studies indicate that $NH_4{^+}$ ions in Tutton salts play an important role in the changes of the crystal structure at high temperatures.