• 자원리싸이클링
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• 제13권4호
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• pp.23-31
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• 2004

수산물 처리시 폐기물로 발생하는 Undaria pinnatifida 를 $Pb^{2+}$ 가 함유된 폐수의 흡착처리시 흡착제로 활용하는 방안을 검토하였다. 성분분석 결과, Undaria pinnatifida는 주로 탄화수소화합물로 구성되어 있었으며 비표면적이 상당히 높아 흡착제로서의 잠재적 활용도가 큰 것으로 파악되었다. Undaria pinnatifida 입자의 Electrokinetic Potential은 pH 8 부근에서 음의 최대값을 보였으며 전 pH 범위에 걸쳐 음으로 하전되어 양이온의 흡착에 적합한 것으로 검토되었다. $Pb^{2+}$는 실험조건에서 반응개시 수 분 이내에 대부분이 흡착되었으며 평형에 도달하는 시간은 약 30분 정도인 것으로 나타났다. 또한, Undaria pinnatifida 표면에 대한 $Pb^{ 2+}$의 흡착은 Freundlich Isotherm 을 따르는 것으로 관찰되었으며 발열반응의 특성을 확인하였다. 산에 의한 흡착제의 전처리는 흡착능을 향상시켰으나 염기로 전처리할 경우에는 오히려 흡착능이 저하되었다. Undaria pinnatifida 표면에 존재하는 작용기들과 $Pb^{ 2+}$ 와의 Organometallic Complex 형성이 $Pb^{ 2+ }$의 흡착에 주요하게 작용하는 것으로 파악되었으며, 경쟁적 흡착질의 존재, ionic Strength 의 변화, 그리고 착화합물제가 수중에 공존할 경우 $Pb ^{2+}$ /의 흡착성이 상당한 영향을 받는 것으로 관찰되었다.

• 한국대기환경학회지
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• 제21권4호
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• pp.439-458
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• 2005

An automated analysis system for water soluble constituents in $PM_{2.5}$ has been developed. The system consists of a high capacity multi tube diffusion scrubber (MTDS), a low temperature particle impactor (LTPI), and two ion (anion and cation) chromatography (IC) systems. Atmospheric particles have been collected by passing sample air through a thermostated MTDS followed by a LTPI. This system allows simultaneous measurements of soluble ions in $PM_{2.5}$ at 30 minutes interval. At the air sampling flow rate of 1.0L/min, the detection limits of the overall system are in the order of tens of $ng/m^3$. This system has been successfully used for the measurement of particulate components of Seoul air from April 2003 to January 2004. $SO_4^{2-},\;NO_3^-,\;NH_4^+,\;NO_2^-,\;Cl^-,\;Na^+,\;K^+,\;Ca^{2+},\;and\;Mg^{2+}$ are the major ionic species for $PM_{2.5}$ at Seoul. Among them, $SO_4^{2-},\;NO_3^-\;and\;NH_4^+$ are the most abundant ions, contributed up to $86\%$ of the total and the concentrations were higher than those in any other urban sites in the world except for Chinese cities. There are high pollutant episodes which contribute about $15\~20\%$ of annual average values of the major ions. During the episode, the all parcels were transported from the asian continent and $PM_{2.5}$ were significantly neutralized. This suggests that aged and long range transported pollutants caused the high pollutant episodes. They showed a distinct daily and seasonal variations:they showed a peak in the early morning caused by the night-time accumulation of particulate matters. Atmospheric reactions including gas-to-particle reactions and inter-particle reactions and meteorological parameters including relative humidity and ambient temperature were described with related to the $PM_{2.5}$ 5 concentrations. All of the ionic species showed higher concentrations during the spring than those for summer and winter.

• Ocean and Polar Research
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• 제37권2호
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• pp.127-140
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• 2015

A continuous series of 60 snow samples was collected at a 2.5-cm interval from a 1.5-m snow pit at a site on the Styx Glacier Plateau in Victoria Land, Antarctica, during the 2011/2012 austral summer season. Various chemical components (${\delta}D$, ${\delta}^{18}O$, $Na^+$, $K^+$, $Mg^{2+}$, $Ca^{2+}$, $Cl^-$, $SO_4{^2-}$, $NO_3{^-}$, $F^-$, $CH_3SO_3{^-}$, $CH_3CO_2{^-}$ and $HCO_2{^-}$) were determined to understand the highly resolved seasonal variations of these species in the coastal atmosphere near the Antarctic Jang Bogo station. Based on vertical profiles of ${\delta}^{18}O$, $NO_3{^-}$and MSA, which showed prominent seasonal changes in concentrations, the snow samples were dated to cover the time period from 2009 austral winter to 2012 austral summer with a mean accumulation rate of $226kgH_2Om^{-2}yr^{-1}$. Our snow profiles show pronounced seasonal variations for all the measured chemical species with a different pattern between different species. The distinctive feature of the occurrence patterns of the seasonal variations is clearly linked to changes in the relative strength of contributions from various natural sources (sea salt spray, volcanoes, crust-derived dust, and marine biogenic activities) during different short-term periods. The results allow us to understand the transport pathways and input mechanisms for each species and provide valuable information that will be useful for investigating long-term (decades to century scale periods) climate and environmental changes that can be deduced from an ice core to be retrieved from the Styx Glacier Plateau in the near future.

• 생태와환경
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• 제51권4호
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• pp.354-364
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• 2018

본 연구는 2008년부터 2016년까지 한강 지류 중랑천을 대상으로 수환경 변화에 따른 어류 군집 양상을 파악하고자 실시하였다. 조사결과, 중랑천에서 서식하는 어류는 총 9과 37종 8,421개체로 나타났으며 과별 출현 종수는 잉어과에서 23종(62.2%)으로 가장 많은 종이 출현하였고, 생태계교란종 및 외래종은 모두 강우기 후 출현하는 특성을 보였다. 수질변화에 따르면, BOD, EC, TN, TP의 변화는 강우량의 증가에 따라 감소하는 양상을 보이는 반면, SS 변화는 증가하는 양상을 보였다. 지점간 CA결과 한강 본류와 인접한 St. 7과 St. 1, 3, 5가 어류의 출현양상 차이를 보였으며, PCA 분석결과 상류에서 하류, 강우기 전과 후의 어류출현양상과 유기오염지표의 변화 양상을 보였다.

• 한국대기환경학회지
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• 제17권2호
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• pp.133-145
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• 2001

The receptor modeling is one of the statistical methods to achieve reasonable air pollution strategies. The pur-pose of this study was to survey the concentration variability oi inorganic elements and ionic species in the PM-10 particles, to qualitatively characterize emission sources by an advanced algorithm called positive matrix factoriza-tion(PMF) as a receptor model that can strictly provide results in every loading matrix. A total of 254 samples was collected by a PM-10 high volume air sampler from Mar. 1997 to Feb. 1998 in Kyung Hee University at Suwon Campus. Fourteen chemical species(Zn, Cu, Fe, Pb, Al, Mn, $Na^{+}$, NH$_4$+, $K^{+}$, $Mg^{2+}$, $Ca^{2+}$, $SO_4^{2-}$, $NO_{3}^{-}$, and $Cl^{-}$) were determined by AAS and IC methods. The study results showed that the average monthly concentration of PM-10 particles were 86.3$\mu\textrm{g}$/$\textrm{m}^3$ in March (maximum) and 28.5$\mu\textrm{g}$/$\textrm{m}^3$ in August(minimum), respectively. The concentrations of Na+, NH$_4$+, $K^{+}$ and $Cl^{-}$ in winter, $Mg^{2+}$, $Ca^{2+}$ and $NO_{3}^{-}$, in spring, and $SO_4^{2-}$ in summer showed the largest peak concentration for the respective season. Through and app-lication of a PMF program of Pm-10 concentration data of Suwon, 9 sources were qualitatively identified , such as incineration source, oil burning source, soil related source, open burning source automobile source, coal burning sources, secondary sulfate related source, and secondary nitrate related source.

• Bulletin of the Korean Chemical Society
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• 제34권12호
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• pp.3609-3614
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• 2013

Orthorhombic and hexagonal lanthanum(III) hydroxycarbonate ($LaCO_3OH$) and $Ln^{3+}$-doped $LaCO_3OH$ ($LaCO_3OH:Ln^{3+}$, where Ln = Ce, Eu, Tb, and Ho) powders were prepared by a hydrothermal reaction under ambient pressure and characterized by thermogravimetry, powder X-ray diffraction, infrared and luminescence spectroscopy, and field-emission scanning electron microscopy. The polymorph of $LaCO_3OH$ depended on the reaction temperature, inorganic salt additive, species of $Ln^{3+}$ dopant, and solvent. The calcination of orthorhombic $LaCO_3OH:Ln^{3+}$ (2 mol %) powers at $600^{\circ}C$ yielded a mixture of hexagonal and monoclinic $La_2O_2CO_3:Ln^{3+}$ powders. The relative quantity of the latter increased with decreasing ionic radius of the $Ln^{3+}$ dopant ion and increasing doping concentrations. On the other hand, the calcination of hexagonal $LaCO_3OH:Ln^{3+}$ (2 mol %) powders at $600^{\circ}C$ resulted in a pure hexagonal $La_2O_2CO_3:Ln^{3+}$ powder, regardless of the species of $Ln^{3+}$ ions (Ln = Ce, Eu, and Tb). The luminescence spectra of $LaCO_3OH:Ln^{3+}$ and $La_2O_2CO_3:Ln^{3+}$ were measured to examine the effect of their polymorph on the spectra.

• 공업화학
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• 제18권5호
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• pp.454-458
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• 2007

본 연구는 알루미나를 이용하여 수용액 중에 존재하는 $Ca^{2+}$, $Mg^{2+}$, $Sr^{2+}$, $SO{_4}^{2-}$, $NO{_3}^-$, $Cl^-$ 이온의 제거 특성을 분석하기 위하여 실시하였다. 알루미나는 $Al(NO_3)_3{\cdot}9H_2O$와 $NH_4OH$를 사용하여 합성한 수화물을 $450{\sim}750^{\circ}C$로 5 h 동안 열처리하고 FT-IR과 Brunauer-Emmett-Teller (BET)법으로 물성을 분석하였다. 실험결과에 의하면 알루미나의 비표면적은 열처리 온도가 증가하면 감소하는 특성을 나타내었다. 알루미나에 의한 흡착능은 $SO{_4}^{2-}$와 $NO{_3}^-$가 각각 23 mg/g와 12.4 mg/g의 값을 보였다. 반면에 $Cl^-$는 4 mg/g으로 비교적 낮은 값을 보였다. 일반적으로 음이온 제거 효율은 알루미나의 제조를 위한 열처리 온도가 증가할수록 감소하였으며, $450^{\circ}C$로 처리한 알루미나의 경우에 가장 좋은 처리 효율을 나타내었다. 양이온인 $Ca^{2+}$, $Mg^{2+}$, $Sr^{2+}$의 제거 효율은 알루미나의 열처리 온도에 비례하여 증가하는 경향을 보였다.

• Korean Chemical Engineering Research
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• 제43권1호
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• pp.33-38
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• 2005

피콜리네이트 착화제가 들어있는 제염 폐액에서 바나듐 및 철 이온종의 평행분배 거동을 pH 값과 조성이 다른 여러 조건에서 모사하였다. 피콜리네이트 대 바나듐의 몰비를 일정한 값으로 고정하고 금속 이온의 농도를 변화시킬 경우 평행분배 곡선의 형태는 바나듐에 대한 피콜리네이트의 농도가 6배인 고농도 및 3배인 저농도 LOMI 제염 조건의 용액에서 모두 크게 바뀌지 않았다. 그러나 저농도 피콜리네이트 조건의 용액에서는 철(II)-피콜리네이트의 평행분배 곡선의 형태가 많이 변화하였는데, 이와 같은 현상은 용액에 들어있는 철에 대한 피콜리네이트의 상대적인 양이 부족하기 때문에 일어나며 바나듐(III) 및 철(II) 이온종이 피콜리네이트 착화물을 형성하는 안정도 상수(stability constant)의 차이에서 비롯된다. 본 연구에서 구한 평형분배 곡선은 이온교환 조작과 같은 LOMI 제염 폐액의 처리 과정에서 용액의 조건 변화에 따른 반응 현상을 예측하거나 이해하는데 매우 유용하게 활용될 수 있다.

• Bulletin of the Korean Chemical Society
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• 제29권7호
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• pp.1364-1368
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• 2008

The activity of the catalytic system composed of Fe$(acetylacetonate)_3$ (Fe$(acac)_3$), triphenylphosphine, and diethylaluminum chloride for the dimerization of bicyclo[2.2.1]hepta-2,5-diene (2,5-norbornadiene, NBD) to produce hexacyclic endo-endo dimer (hexacyclo[$7.2.1.0^{2,8}.1^{3,7}.1^{5,13}.0^{4,6}$]tetradec-10-ene, Hnn) was significantly enhanced by the presence of $AlCl_3$, especially at the molar ratios of NBD/Fe$(acac)_3$ of 500. XPS analysis of the catalytic systems clearly demonstrates that $AlCl_3$ facilitates the reduction of Fe$(acac)_3$ to form active species, Fe(II) and Fe(0) species. The layer separation was observed when [BMIm]Cl was used along with $AlCl_3$, but catalyst recycle was not very successful.

• 한국재료학회지
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• 제14권3호
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• pp.229-234
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• 2004

All the applications of natural zeolites make use of one or more of their physical and chemical properties: adsorption, ion-exchange and related molecular sieve properties, dehydration and rehydration, and siliceous composition. Accordingly, the applications of zeolite have been carried out in the various aspects because of its large cation exchange capacity and adsorption properties. In this paper, the adsorption effect of heavy metal ions in wastewater on zeolite mineral by batch adsorption process is studied. The amounts of adsorbed ions were variable by original pH and ionic concentration, especially original pH of solution had an important effect on the adsorption. In case of low pH solution, e.g. below 3.0, clinoptilolite adsorbed $Pb^{2+}$ ,$ Cd ^{2+ }$ , $Cu^{2+}$ and $Zn^{ 2+}$ , but mordenite almost did not adsorb except $Pb^{2+}$ . Under the same conditions, these ions were more adsorbed on clinoptilolite than on mordenite mineral. The velocity of adsorption was relatively fast and it was confirmed by shaking test that the equilibrium of adsorption could be attained in about one hour. The species of exchangeable cation of zeolite had an effect on its removing ability and zeolite of the sodium-exchanged type was the best.