• 농업과학연구
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• 제46권4호
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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.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 추계학술발표회
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• pp.99-102
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• 2001

The soil-to-air fluxes of three PAHs(Phenanthrene, Pyrene, Benzo(a)pyrene) from a laboratory contaminated forest soil were investigated in experimental microcosms. The effects of soil temperature(45$^{\circ}C$, $25^{\circ}C$, 5$^{\circ}C$) and relative humidity(0%, 100%) were investigated according to existence of the humic layer(O layer) over the mineral layer(A layer). Volatilization flux experiments were carried out for a period of 96 hrs. The resulting PAHs volatilization fluxes from the different conditions were quantified and compared. In the mineral layer, highest volatilization flux among the individual PAHs was Phenanthrene >Pyrene> Benzo(a)pyrene on the conditions of 45 $^{\circ}C$, RH=100%. In the humic layer over the mineral layer, maximum volatilization flux was Phenanthrene on the condition of 45$^{\circ}C$, RH=0%. Results from flux experiments showed that volatilization fluxes of PAHs were dependent on soil temperature. Existance of humic layer over the mineral layer delayed transportation to the air of especially heaveir molecular PAHs. But, if humic layer is contained water sufficiently, it is possible that volatilization fluxes are enhanced by water convective flux according to variation of soil temperature and air relative humidity.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.266-269
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• 2000

To understand the gaseous behaviour of volatile organic compounds in the unsaturated zone, their volatilization coefficient k$_{Lg}$ is evaluated. An experiment is conducted to examine the dependence of k$_{Lg}$ on the concentration of the dissolution, presence of unsaturated zone and depth of the unsaturated zone. The results show that the volatilization coefficient is not dependent on the concentration under the constant temperature and pressure. It is also find that k$_{Lg}$ depends on the presence of the unsaturated zone rather than its depth.depth.

• 한국환경농학회지
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• 제28권3호
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• pp.233-237
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• 2009

It has widely been observed that the effect of elevating atmospheric $CO_2$ concentrations on rice productivity depends largely on soil N availabilities. However, the responses of ammonia volatilization from flooded paddy soil that is an important pathway of N loss and thus affecting fertilizer N availability to concomitant increases in atmospheric $CO_2$ and temperature has rarely been studied. In this paper, we first report the interactive effect of elevated $CO_2$ and temperature on ammonia volatilization from rice paddy soils applied with urea. Urea labeled with $^{15}N$ was used to quantitatively estimate the contribution of applied urea-N to total ammonia volatilization. This study was conducted using Temperature Gradient Chambers (TGCs) with two $CO_2$ levels [ambient $CO_2$ (AC), 383 ppmv and elevated $CO_2$ (EC), 645 ppmv] as whole-plot treatment (main treatment) and two temperature levels [ambient temperature (AT), $25.7^{\circ}C$ and elevated temperature (ET), $27.8^{\circ}C$] as split-plot treatments (sub-treatment) with triplicates. Elevated temperature increased ammonia volatilization probably due to a shift of chemical equilibrium toward $NH_3$ production via enhanced hydrolysis of urea to $NH_3$ of which rate is dependent on temperature. Meanwhile, elevated $CO_2$ decreased ammonia volatilization and that could be attributed to increased rhizosphere biomass that assimilates $NH_4^+$ otherwise being lost via volatilization. Such opposite effects of elevated temperature and $CO_2$ resulted in the accumulated amount of ammonia volatilization in the order of ACET>ACAT>ECET>ECAT. The pattern of ammonia volatilization from applied urea-$^{15}N$ as affected by treatments was very similar to that of total ammonia volatilization. Our results suggest that elevated $CO_2$ has the potential to decrease ammonia volatilization from paddy soils applied with urea, but the effect could partially be offset when air temperature rises concomitantly.

• The Korean Journal of Ceramics
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• 제6권4호
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• pp.343-347
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• 2000

The alkali volatilization of TV screen glass melts with various $K_2$O/R$_2$O mole fraction was investigated by dependence of weight loss on time. The melt conductivity was also determined to evaluate relative alkali diffusion in melts. Based on the results of time dependence and compositional dependence of volatilization combining the results of conductivity, the rate determining process of the volatilization was suggested. From the viewpoint of the production and the application of TV glass it was also discussed a correlation between the dependence of properties on $K_2$O/R$_2$O and the present commercial composition.

• 한국토양비료학회지
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• 제13권1호
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• pp.7-11
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• 1980

질소비료(窒素肥料)의 시용량(施用量)에 따른 암모니아의 휘산량(揮散量)을 밝히기 위하여 토양 25g에 요소태질소(尿素態窒素)를 3.75mg, 7.5mg, 11.25mg 씩 가(加)하여 7 주간(週間) $35{\sim}40^{\circ}C$로 보온 처리한 결과(結果)는 다음과 같다. 요소(尿素)의 시용량(施用量)이 증가함에 따라 암모니아의 휘산량(揮散量)이 증가하였는데 그 증가는 암모니아의 생성증가에 따른 토양반응의 상승(上昇)과 밀접(密接)한 관계가 있다. 2. 석회(石灰)의 과용(過用)은 요소(尿素)의 가수분해(加水分解)와 토양질소의 유효화를 휘제(揮制)하여 암모니아의 휘산량(揮散量)을 줄였다. 이 경향(傾向)은 토양의 pH가 8.0 이상(以上)이 되면 더욱 심(甚)해졌다.

• 한국환경과학회지
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• 제18권12호
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• pp.1325-1330
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• 2009

The fumigant 1,3-dichloropropene (1,3-D) was recently proposed as a direct replacement for methyl bromide ($CH_3Br$) in soil fumigation. This study was conducted to better understand behavior phase partitioning, diffusion and volatilization of 1,3-D as affected by isomer. The Henry's law constant(KH) of cis-1,3-D and trans-1,3-D was 0.058 and 0.037 at $20^{\circ}C$, respectively. $K_H$ of cis form of 1,3-D was higher than that of trans form of 1,3-D. To compare with volatilization of 1,3-D isomer, soil column [70 cm (length)${\times}$12 cm (i.d.)] included a shank injection at 30 cm with 300 kg $ha^{-1}$. Maximum cis-1,3-D and trans-1,3-D concentration reached 57 mg $L^{-1}$ and 39 mg $L^{-1}$ at 30 cm depth at 1h after application. Cumulatively, after 10 days, 51.8% and 43.57% of applied cis-1,3-D and trans-1,3-D was emitted via volatilization, respectively. The total losses of cis-1,3-D were significantly greater than that of trans-1,3-D. Finally, cis-1,3-D and trans-1,3-D, such as isomer are dominant of 1,3-D fates in soil.

• 아시안잔디학회지
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• 제6권1호
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• pp.23-28
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• 1992

Urea, the major N source of world agriculture involves a serious urea-N loss through NH$_3$volatilization. Approaches to decrease N loss include using urease inhibitors in view of the environmental protection and the increase of urea-N efficiency. The purpose of laboratory researches was toassess the potential value of urease inhibitors to increase urea-N efficiency in soil and Kentucky blue-grass(Poa Pratensis L.) turf. The activity of urease inhibitors Phenyiphosphorodiamjdate(ppD) and N-(n-butyl) thiophosphoric triamjde(NBPT) measured to break-down ammonia volatilization. The soil and turf used in this project were from the fairway in one of the Korean gof course. The researches were carried out for two weeks to measure the urease activities on urea hydrolysis under four temperatures (10~ 40$^{\circ}C$) and for one week on turfgrass using forced-draft system. Results indicated that Urea-N involves considerable loss through gaseous NH$_3$ by urease activities in plant-soil systems. Urease inhibitors PPD and NBPT have potential value for increasing N use efficiency by reduing NH$_3$ volatilization. NBPT deserves futher evaluation as fertilizer amendment than PPD use of urea in turf industries.

• 한국토양비료학회지
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• 제46권6호
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• pp.610-614
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• 2013

Massive intercalation of urea into montmorillonite (MUCH) was recently proposed to enhance urea use efficiency through smart suppression of emission of $NH_3$ and NOx. This study was to synthesize citrate-incorporated MUCH (Cit-MUCH) which can enhance suppression of $NH_3$ volatilization. The XRD pattern of Cit-MUCH was very similar to that of MUCH to indicate successful incorporation of citric acid into MUCH. Incorporation of citric acid was confirmed by the existence of $COO^-$ symmetric stretching vibration. During the initial 4 days after application, $NH_3$ volatilization from both bare and perilla-planted soils was much more suppressed by application of Cit-MUCH than MUCH. A peak volatilization rate decreased from 28.3 N mg $m^{-2}\;h^{-1}$ of MUCH-broadcasted soil to 22.2 N mg $m^{-2}\;h^{-1}$ of Cit-MUCH-broadcast soil. $NH_3$ volatilization was less in planted soil than bare soil for 72 hrs after application. These results showed that incorporation of citric acid led to increase in suppression of ammonia volatilization from urea-applied soils.

• 한국토양비료학회지
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• 제38권6호
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• pp.321-327
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• 2005

LCU와 요소를 담수토양의 전층에 혼합처리한 후 $30^{\circ}C$의 항온 시험 결과, LCU와 요소 시용구에서 모두 표면수의 $NH_4-N$ 농도와 pH가 증가함에 따라 암모니아 휘산량은 지수함수적으로 증가하였다. 그러나 LCU 시용구에서는 표면수의 $NH_4-N$ 농도가 $10mg\;L^{-1}$ 이하이었고 휘산량도 $0.5kg\;N\;ha^{-1}$이었다. 반면에 요소 시용구에서는 $NH_4-N$ 농도가 $40mg\;L^{-1}$까지 증가하였고, 암모나아 휘산량도 $1.6kg\;N\;ha^{-1}$까지 증가하여 암모니아 휘산량은 $NH_4-N$ 농도와 상관이 높았다. 표면수의 pH와 암모니아 휘산량과의 상관관계를 보면 LCU와 요소 시용구에서 모두 표면수의 pH가 7.0-8.0일 때는 암모니아 휘산량이 $0.2kg\;N\;ha^{-1}$ 이하로 뚜렷한 증가가 없었으나 pH가 8.0 이상일 때에는 pH가 증가할수록 암모니아 휘산량이 급격히 증가하였다. 토양 $NH_4-N$ 농도는 이앙 후 20일경에 가장 높았는데 LCU 100% 처리구에서 $38mg\;kg^{-1}$, 요소 시용구에서 $36mg\;kg^{-1}$, LCU 80% 처리구에서 $28mg\;kg^{-1}$ 순으로 높았다. 벼 이앙재배에서 완효성질소비료인 LCU를 표준 시비량의 80%과 100% 수준으로 시용하여 관행 요소 시용에 대한 암모니아 휘산에 의한 손실 절감 효과를 검토하였다. 표면수의 $NH_4-N$ 농도는 요소시용구에서는 추비 후 $NH_4-N$ 농도가 $8-10mg\;L^{-1}$로 크게 높아졌으나, LCU 처리구에서는 생육기간동안 $1mg\;L^{-1}$ 이하로 낮았다. 요소 시용구에서의 암모니아 휘산량은 추비 시용 후 급격히 증가하였고, 시비질소에 대한 총 휘산량은 $4.9-8.4kg\;N\;ha^{-1}$ 로서 연차간에 차이를 보였다. 한편 LCU 시용시 암모니아 휘산량은 LCU의 시비량에 관계없이 $1.2-1.8kg\;N\;ha^{-1}$ 였으며, 연차간에도 휘산량의 차이를 보이지 않았다. 따라서 벼 기계이앙재배시 요소에 비하여 완효성 질소비료인 LCU의 시용으로 암모니아 휘산은 75-79% 경감되었다.