• Asian Journal of Atmospheric Environment
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• v.5 no.2
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• pp.97-104
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• 2011

Recent studies have indicated that the observed nitric acid ($HNO_3$) uptake rates ($R_{HNO_3}$) onto dust particles are much slower than $R_{HNO_3}$ used in the previous modeling studies. Three factors that possibly affect $R_{HNO_3}$ onto dust particles are discussed in this study: (1) the magnitude of reaction probability of $HNO_3$ (${\gamma}_{HNO_3}$), (2) aerosol surface areas, and (3) gas-phase $HNO_3$ mixing ratio. Through the discussion presented here, it is shown that the use of accurate ${\gamma}_{HNO_3}$ is of primary importance. We suggest that the use of ${\gamma}_{HNO_3}$ values between $\sim10^{-3}$ and $\sim10^{-5}$ produces more realistic results than the use of ${\gamma}_{HNO_3}$ values between $\sim10^{-1}$ and $\sim10^{-2}$ does, more accurately modeling the nitrate formation characteristics on/in dust particles. We also discuss two different types of aerosol surface area, active and geometric, since the use of different aerosol surface areas often leads to an erroneous result in $R_{HNO_3}$. In addition, the levels of the gas-phase $HNO_3$ are investigated with the example cases of TRACE-P DC-8 flights in East Asia. The $HNO_3$ levels were found to be relatively high, indicating that they can not limit nitrate formation in dust particles.

• Journal of Korean Society for Atmospheric Environment
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• v.9 no.2
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• pp.154-159
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• 1993

Theoretical prediction of the equilibrium of temperature and relative humidity dependance involving $HNO_{3(g)}-NH_{3(g)}$ and $NH_4NH_{3(s, aq)}$ was compared with atmospheric measurement of particulate nitrate$(NO_3^-)$, Ammonia-Nitric Acid partial pressure product $([$NH_{3(g)}][HNO_{3(g)}]ppb^2$) by a triple filter pack sampler from Oct 1991 to July 1992. The measured $HNO_3NH_3$ concentration product K was greater than equilibrium constant $K_p$ calculated from thermodynamic data of $NH_4NO_{3(s, aq)}-HNO_{3(g)}-NH_{3(g)}$ during fall, winter and spring. But K was lower than $K_p$ in summer. K was greater than $K_p$ as the result of supersaturation by air pollution, particularly anthropogenic $NH_3$.The reason of $K < K_p$ was due to removal of particulate nitrate$(NO_3^-)$ by rainout and washout. $NH_4NO_3$ which consists mainly of particulate nitrate is formed by reaction between $HNO_3$ and $NH_3$. As a result of the removal of particulate nitrate$(NO_3^-)$ by rainout and washout, concentrations of $HNO_3$ and $NH_3$ are decreased by equilibrium transfer(Le Chatelier's Law) in atmosphere.

• Journal of Korean Society for Atmospheric Environment
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• v.8 no.3
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• pp.198-203
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• 1992

Theoretical predictions of the atmospheric equilibrium involving $HNO_3, NH_3 and NH_4NO_3$ were compared with atmospheric measurements of particulate nitrate$(NO_3^-)$, $HNO_3$ and $NH_3$ concentration by triple filter pack sampler and Andersen air sampler in Seoul from 8th to 11th Oct 1991. The measured $HNO_3-NH_3$ concentration product K was higher than equilibrium costant Kc calculated from thermodynamic data of $HN_4NO_{3(s)} -HNO_{3(g)} -NH_{3(g)}$. The cause of K is greater than Kc was the result of air pollution, partcicularly anthropogenic $NH_3$.

• Applied Chemistry for Engineering
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• v.23 no.2
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• pp.148-152
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• 2012

Anatase and anatase/rutile $TiO_2$ samples were prepared at $HNO_3$/TTIP molar ratio of 0.1, 0.5, 1.0, and 1.5 to study the effects of the physical properties of $TiO_2$ on photocatalytic decomposition of methylene blue. The physical properties of the samples were measured with XRD, SEM, TEM, BET, FT-IR, and UV-vis spectroscopy. Anatase phase was observed at $HNO_3$/TTIP of 0.1 and anatase/rutile phases were observed at $HNO_3$/TTIP of 0.5~1.5. Rutile crystal phase, mesopore size between $TiO_2$ nanoparticles, and surface OH group on $TiO_2$ sample were gradually increased with increasing the molar ratio of $HNO_3$/TTIP and the residual methylene blue concentration before UV irradiation decreased from 78.0 to 53.3%. After UV irradiation, the residual methylene blue concentrations of the samples prepared at $HNO_3$/TTIP of 0.1, 0.5, 1.0, and 1.5 were 20, 14, 11, and 23%, respectively, and the sample prepared at $HNO_3$/TTIP of 1.0 showed the best photocatalytic ability.

• Proceedings of the Korea Society of Poultry Science Conference
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• 2001.11a
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• pp.102-103
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• 2001

Two experiments were conducted to investigate the effects of feather digests on the growth of broiler chicks and taurine content in the broiler meat. In Experiment 1, a total of 40 broiler chickens(Ross) were assigned to 4 dietary treatments: control(T1), regular feather meal(FM) diet(R-FM, T2), NaOH treated FM diet(NaOH-FM,T3), HNO3 treated FM diet(HNO3-FM,T4). In Experiment 2, a total of 70 broiler chickens were assigned to 7 dietary treatments: T1~T4(same as those of Exp. 1), modified HNO3 treated FM diet(M-HNO3-FM,T5), hair meal diet(HM,T6) and 0.22% cystine supplemented diet(CYS,T7). Feather meals and hair meal were supplemented at the 5% in the diet. In Experiment 1 and 2, weight gain of chicks fed R-FM and NaOH-FM tended to be higher than those of the control and HNO3-FM. In Experiment 2, weight gain of chicks fed CYS was highest followed by NaOH-FM, HM, M-HNO3-FM, HNO3-FM, control and R-FM. In Experiment 1, taurine content in breast muscle of chicks fed NaOH-FM was significantly higher(P<0.05) than that of control. In Experiment 2, taurine content in breast muscle of chicks fed NaOH-FM and CYS tended to be higher than that of other groups. Taurine content in leg muscle was significantly different among treatments as NaOH-FM and R-FM being highest followed by M-HNO3-FM, CYS, control, HNO3-FM and BM. Taurine content in the liver(Exp. 1 and 2) and heart(Exp. 2) were not significantly affected by treatments. These results indicated that 5% NaOH-FM in the diet was effective in increasing taurine content in breast and leg muscle of broiler chicks.

• Journal of Korean Society for Atmospheric Environment
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• v.8 no.1
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• pp.68-73
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• 1992

A study on the formation of particulate nitrate$(NO_3^-)$ and gaseous nitrate$(HNO_3)$ in the atmosphere was carried out in Seoul from Oct 8 to 11 1991. To collect $NO_3^-$ and $HNO_3$ in the ambient air, dual filter pack sampler (47mm$\phi$) was used. In the dual filter pack sampler, the first filter was Teflon filter (poresize 1$\mum$) for collection of $NO_3^-$ and the second filter was Nylon filter (poresize 0.45 $\mum$) for $HNO_3$. Particulate nitrate$(NO_3^-)$ and Sulfate ions were analysed by Ion chromatography. $HNO_3$ concentration was higher in the day time $(9.93\mug/m^3)$ than the night time$(3.50\mug/m^3)$, and Particulate nitrate$(NO_3^-)$ concentration was higher in the night time and early morning$(6.21\mug/m^3)$ than the day time$(4.31\mug/m^3)$. The conversion rate of $NO_x$ to total nitrate$(NO_3^-, HNO_3)$ was 7.57%/hr in the day time and 4.79%/hr in the night time, and total average conversion rate was 5.60%/hr.

• Analytical Science and Technology
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• v.18 no.2
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• pp.112-119
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• 2005

This study reports on the efficiency of cleaning enameled magnet wire using a sulfuric acid $H_2SO_4$ and removal of dissolved organic material using hydrogen peroxide $H_2O_2$ and nitric acid $HNO_3$ at $80^{\circ}C$. The method involves the addition of pure $H_2SO_4$ and $H_2O_2$ or $HNO_3$. Layers of enameled organic material were dissolved by 90% $H_2SO_4$ and the solution was maintained as 35% $H_2O_2$ or 60% $HNO_3$. $H_2O_2$ content in aqueous $H_2O_2$ was maintained as 8.8 : 1.0. An initial concentration of $H_2SO_4$ in dissolution conditions was accomplished within 15 min, with a stripping time of about 2 h. The concentrations of $H_2O_2$ and $HNO_3$ in the processing bath were relatively low, but sufficient enough to produce an effective amount of power in the bath for the removal of the enamel material. The cleaning effect of enameled organic material involves the dehydration by $H_2SO_4$ and the oxidation by $H_2O_2$ or $HNO_3$.

• Journal of Korean Society for Atmospheric Environment
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• v.15 no.3
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• pp.305-315
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• 1999

The annular denuder system(ADS) was used to determine characteristics of acidic air pollutants and $PM_{2.5}$ species in Seoul-metropolitan areas. All measurements were done simultaneously in downtown(Kwanghwamun, Mullae, Chamshil, Ssangmun dongs) and outskirts(Puch n, Kuri cities) during four seasons. The samples were analyzed using ion chromatography for gas-phase matters(HCl, $HNO_2$, $HNO_3$ and $SO^2$) and particulate phase matters($Cl^-$, $NO^{2-}$, $NO_3^-$, $SO_4^{2-}$, $Na^+$, $NH_4^-$ and $Ca^{2+}$) and was measured fine particles($PM_{2.5}$). The seasonal mean concentrations of HCl, HNO2, HNO3 and SO2 in downtown and outskirt areas were very similar. All chemical species monitored from this study showed seasonal variations. Nitric acid(HNO3) and Nitrous acid(HNO2) were showed higher concentrations during the summer. $PM_{2.5}$, $SO_4^{2-}$, $NH_4^-$, $NO_3^-$ and $Cl^-$ in the particulate phase matters were higher levels during the winter months. The concentrations of these components were 54.8, 3.82, 2.49, 1.80 and 1.02$\mu\textrm{g}$/㎥, respectively.

• Journal of Environmental Impact Assessment
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• v.29 no.3
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• pp.198-209
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• 2020

In this study, electrospun nanofibers made of PAN (polyacrylonitrile) were activated through a physical method to obtain an optimized pore structure. In particular, to enhance the surface alkalinity, the activated carbon fibers (ANFs) were impregnated with tetraethylenepentamine (TEPA) with the aid of HNO₃. Then, the low level (3,000 ppm) CO₂ adsorption capacity for each ANF sample was evaluated. The specific surface area of ANFs increased from 308.4 ㎡/g to 839.4 ㎡/g and the total pore volume increased from 7.882 ㎤/g to 27.50 ㎤/g. Although the TEPA impregnation reduced the specific surface area and pore volume of the ANFs due to blocking of micropores, the HNO₃ pre-oxidation enhanced the amino groups tethered, increasing the amine content from 6.42% to 17.19%, and finally, increased the adsorption capacity of CO₂. This study showed that the sample 60-ANF-HNO₃-TEPA, which was activated for 60 minutes and was impregnated with HNO₃ and TEPA, had the best adsorption capacity for low level (0.3%) CO₂ (in a binary mixture with N₂).

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.5 no.2
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• pp.133-143
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• 2007

This study was performed to evaluate the co- and sequential separation of Tc, Np and U from the simulated multi-component HLW solution by a TBP (tributyl phosphate)-TOA (tri- octyl amine)/NDD $(n-dodecane)-HNO_3$ extraction system. An optimal condition of (30% TBP-0.5% TOA)/NDD-1 M $HNO_3$ was selected by taking account of a prevention of the 3rd phase and effects of concentration of TBP, TOA and nitric acid on the co-extraction of Tc, Np and U. In that condition, the extraction yields were 81% (Tc), 85% (Np), less than 9% (Am and RE elements), about 8% (Pd), and less than 5% (other elements) so that the system developed for the co-extraction of Tc, Np and U was proved to be available. For that, however, more than 99% of Zr was found to be pre-removed. The co-extracted Tc, Np and U were sequentially separated in order of Tc(stripping agent : 5 M $HNO_3$)${\rightarrow}Np$ by reductive stripping (reductive-stripping agent : 0.1 M AHA)${\rightarrow}U$ (stripping agent : 0.01 M $HNO_3$), and then their separation factors were evaluated. At these conditions, 95% of Tc, 98% of Np and 99% of U could be recovered in each step.