• 농약과학회지
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• 제15권4호
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• pp.441-452
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• 2011

농경지 중 내분비계장애 추정농약의 잔류 실태를 조사하기 위하여 시설재배 토양을 경기도 가평 등 전국 40개 지역에서 총 40점을 채취하여 현재 우리나라에서 분류한 내분비계장애추정농약 40종 중 등록되어 사용중인 alachlor를 포함한 16종의 농약을 대상으로 GC-ECD 및 HPLC-DAD/FLD를 이용한 다성분동시분석법 및 개별분석법으로 분석하였다. 시험농약의 검출한계는 0.0004-0.005 mg/kg이었으며, 각 시험농약의 회수율 72.69-115.28%의 범위였다. 조사대상 토양 40점 중 16점의 시료에서 cypermethrin 등 4종의 내분비계장애추정농약이 검출되어 37.5%의 검출율을 보였다. 그 중 endosulfna은 12지역에서 검출되어 가장 높은 검출빈도를 보였다. 또한 GUS로 판단할 때 대부분의 검출 농약은 지하수를 오염시킬 가능성이 거의 없었으나 살균제 vinclozolin은 약간의 지하수를 오염시킬 가능성이 있는 것으로 추정되었는데 이는 수용성이 높고 토양 흡착성이 낮은 특성 때문인 것으로 보인다.

• 한국재료학회지
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• 제12권11호
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• pp.860-864
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• 2002

$Li^{+}$ extraction reactions with ion-exchange type lithium manganese oxide in an aqueous phase were examined using chemical and x-ray diffraction (XRD) analysis. In the process of extraction reaction, the lithium manganese oxide showed a topotactic extraction of $Li^{+ }$ in the aqueous phase mainly through an ion-exchange mechanism, and the $Li^{+}$ extracted samples indicated a high selectivity and a large capacity for $Li^{+}$ . The electronic structures and chemical bonding properties were also studied using a discrete variational (DV)-X$\alpha$ molecular orbital method with cluster model of (Li$Mn_{12}$ $O_{40}$ )$^{27-}$ for tetrahedral sites and ($Li_{7}$ Mn $O_{38}$ )$^{3}$ for octahedral site in $Li_{1.33}$ $Mn_{1.67}$ / $O_{4}$ respectively. Li in the manganese oxides is highly ionized in both sites, but the net charge of Li was greater for tetrahedral sites than octahedral. These calculations suggest that the tetrahedral sites have higher $Li^{+}$ $H^{+}$ exchangeability than the octahedral sites, and are preferable for the selective adsorption for L $i^{+}$ ions.s.

• 한국환경과학회지
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• 제20권10호
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• pp.1337-1345
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• 2011

The removal performances of divalent heavy metal ions ($Pb^{2+}$, $Cu^{2+}$, $Cd^{2+}$, $Sr^{2+}$ and $Mn^{2+}$) were studied using the Na-P1 zeolite synthesized from Jeju scoria in the batch and continuous fixed column reactor. The uptakes of heavy metal ions by synthetic Na-P1 zeolite decreased in the order of $Pb^{2+}$ > $Cu2^{2+}$ > $Cd^{2+}$ > $Sr^{2+}$ > $Mn^{2+}$ based on the selectivity of each ion to ionic exchange site of Na-P1 zeolite for single and mixed solutions in batch or continuous fixed column reactor. For mixed solution, each heavy metal ion uptake was lower than that in single solution, and especially the uptake for $Mn^{2+}$ decreased greatly. In batch reactor, the uptakes of heavy metal ions by synthetic Na-P1 zeolite were described by Freundlich or Langmuir equation, but they followed the former better than the latter. In continuous fixed column reactor, the maximum ion exchange capacity obtained for each of heavy metal ions, was about 90----- of that in batch reactor. The uptakes of heavy metal ions by synthetic Na-P1 zeolite increased with the increase of initial heavy metal concentration and solution pH, and the decrease of the amount and particle size of synthetic zeolite.

• 한국분말재료학회지
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• 제16권1호
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• pp.22-27
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• 2009

To improve the filtration efficiency of porous materials used in filters, an extensive specific surface area is required to serve as a site for adsorption of impurities. In this paper, a method for creating a hybridized porous alloy using a powder metallurgical technique to build macropores in an Al-4 wt.% Cu alloy and subsequent surface modification for a microporous surface with a considerably increased specific surface area is suggested. The macropore structure was controlled by granulation, compacting pressure, and sintering; the micropore structure was obtained by a surface modification using a dilute NaOH solution. The specific surface area of surface-modified specimen increased about 10 times compare to as-sintered specimen that comprised of the macropore structure. Also, the surface-modified specimens showed a remarkable increase in micropores larger than 10 nm. Such a hybridized porous structure has potential for application in water and air purification filters, as well as membrane pre-treatment and catalysis.

• 한국대기환경학회지
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• 제27권1호
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• pp.63-72
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• 2011

This study describes the impact of positive sampling artifact caused by a filter-based sampling in the determination of ambient organic carbon (OC). Three different sampling media combinations were employed for this investigation: (1) Quartz filter-alone (Q-alone), (2) quartz filter behind quartz-fiber filter (QBQ), and (3) quartz filter and quartz filter behind Teflon filter (Q-QBT). The measurement of ambient OC was carried out at a semi-urban site near oceanside at the end of November of 2008. It was found that Q-alone sampling configuration resulted in a higher OC than QBQ and Q-QBT by 14% and 28%, respectively due to no correction for positive artifact caused by adsorption of gas-phase OC onto the filter. A lower quantity of OC was collected from the backup quartz filter on QBQ than that from Q-QBT. A possible explanation is that the front quartz filter of QBQ was not fully saturated with gas-phase OC during the sampling period, allowing smaller amount of gas-phase OC to reach the backup quartz filter. The contribution of positive artifact to $PM_{2.5}$ mass was approximately 2.15 ${\mu}g/m^3$ which is equivalent to 6% in terms of Q-QBT sampling configuration. The positive artifact was found to be more dominated during summer than during winter, showing temperature dependence. It was concluded that Q-QBT sampling configuration offers less impact of positive artifact on ambient OC sampling than QBQ in quantification of OC.

• 한국자기공명학회논문지
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• 제11권2호
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• pp.95-109
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• 2007

Vanadium-incorporated aluminophosphate microporous molecular sieve VH-SAPO-42 has been studied by electron spin resonance(ESR) and electron spin-echo modulation (ESEM) spectroscopies to determine the vanadium location and interaction with various adsorbate molecules. The results are interpreted in terms of V(IV) ion location and coordination geometry. Assynthesized VH-SAPO-42 contains only vanadyl species with distorted octahedral or trigonal bipyramidal coordination. Vanadium incorporated into H-SAPO-42 occupied extra-framework site. After calcinations in $O_2$ and exposure to moisture, only species A is observed with reduced intensities. Species A is identified as a $VO(H_2O)_2^{2+}$ complex coordinated to three framework oxygen atoms bonded to aluminum. When hydrated VH-SAPO-42 is dehydrated at elevated temperature by calcination, species A loses its water ligand and transforms to $VO^{2+}$ ions coordinated to three framework oxygens (species B). Species B reduces its intensities significantly after treatment with $O_2$ at high temperature, thus suggesting oxidation of $V^{4+}$ to $V^{5+}$. When dehydrated VH-SAPO-42 makes contact with $D_2O$ at room temperature, the ESR signal of species A is regained. The species is assumed as a $VO(O_f)_3(D_2O)_2$ by considering three framework oxygens. Adsorption of deuterated methanol on dehydrated VH-SAPO-42 results in another new vanadium species D, which is identified as a $VO(CD_3OH)_2$ complex. When deuterated ethylene is adsorbed on dehydrated VH-SAPO-42, another new vanadium species E identified as a $VO(C_2D_4)^{2+}$, is observed. Possible coordination geometries of these various complexes are discussed.

• 상하수도학회지
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• 제23권5호
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• pp.599-608
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• 2009

This manuscript covers the results of field investigation and lab-scale experiments to design a double-layered biofilter system to control urban storm runoff. The biofilter system consisted of a coarse soil layer (CSL) for filtration and fine soil layer (FSL) for adsorption and biological degradation. The variations of flow rate and water quality of runoff from a local expressway were monitored for seven storm events. Laboratory column experiments were performed using seven kinds of soil and mulch to maximize pollutants removal. The site mean concentration (SMC) of storm runoff from the drainage area (runoff coefficient: 0.92) was measured to be 203 mg/L for SS, 307 mg/L for $TCOD_{Cr}$, 12.3 mg/L for TN, 7.3 mg/L for ${NH_4}^+-N$, and 0.79 mg/L for TP, respectively. This study employed a new design concept, to cover the maximum rainfall intensity with one month recurrence interval. Effective storms for last ten years (1998-2007) in seoul suggested the design rainfull intensity to be 8.8 mm/hr Single layer soil column showed the maximum removal rate of pollutants load when the uniformity coefficient of CSL was 1.58 and the silt/clay contents of FSL was virtually 7%. The removal efficiency during operation of double layer soil column was 98% for SS and turbidity, 75% for TCODCr, 56% for ${NH_4}^+-N$, 87% for TP, and 73-91% for heavy metals. The hydraulic conductivity of the soil column, 0.023 cm/sec, suggested that the surface area of the biofilter system should be about 1% of the drainage area to treat the rainfall intensity of one month recurrence interval.

• 한국환경보건학회지
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• 제37권2호
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• pp.141-149
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• 2011

This study aimed for developing a two stage dual media filtration system. It has a sand and activated carbon layer above the under-drain system, and a sand layer above the middle-drain system for pretreatment. When retrofitting an old sand filter bed or designing a new one, this technology can substitute the existing sand filter bed without requiring a new plant site. The removal rate of total particle is 93, and 3~7 ${\mu}m$ and 5~15 ${\mu}m$ particles are all 97%. These high removal efficiencies of each pollutant due to adsorption and biological oxidation in activated carbon filter layer. The best backwashing method of two stage dual media filtration system is ascertained by air injection, air + water injection and water injection sequence. In this study, a pilot plant of two stage and dual filtration system was operated for 4 months in water treatment plant. The stability of turbidity was maintained below 1 NTU. The TOC, THMFP and HAAFP were removed about 90% by two stage and dual media filtration system, which is almost 2 times higher than existing water treatment plant.

• 전기화학회지
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• 제2권2호
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• pp.106-111
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• 1999

[ $CaNi_5$ ] 수소저장합금의 전기화학적 충$\cdot$방전 특성에 미치는 MG(mechanical grinding) 영향이 Ar및 $H_2$ 가스분위기에서 조사되었다 MG공정중 $CaNi_5$ 합금은 표면 산화층의 파괴와 재생성 및 산화층 근방의 불균질화로 인하여 MG 15시간 이후부터 CaO와 Ni로 뚜렷한 상분리가 일어났다. $MG-CaNi_5$는 MG시간이 길어질수록 초기의 전기화학적 방전용량은 현저히 감소하였지만 충$\cdot$방전 싸이클의 증가에 따른 용량저하 속도는 $CaNi_5$합금에 비하여 낮았다. MG처리된 $CaNi_5$합금의 퇴화는 MG공정중의 상분리 및 불규칙화에 의한 수소의 가역반응 site의 감소 및 분극저항의 증가, KOH 전해질 내에서 합금 표면의 산화반응에 의한 부동태 피막형성에 기인하는 것으로 판단되었다.

• 대한환경공학회지
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• 제35권12호
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• pp.906-917
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• 2013

본 연구에서는 고상 미세추출법(HS-SPME)을 적용하여 대기환경시료 중 VOCs 분석을 위한 응용성을 평가하고자 하였다. 광범위한 VOCs 검출을 위한 최적 HS-SPME 분석 조건(CAR/PDMS fiber, 30분 시료노출, 도출된 분석조건)에서 VOCs의 검출 한계 농도는 저분자량 화합물인 경우 1~3 ppbv 내외였고, BTEXs 계열 화합물들의 경우에는 0.0005 ppbv 이하의 매우 낮은 농도까지 검출 가능하였다. 다만 fiber들 간의 흡착효율 재현성 평가결과, 동일 fiber에 대하여 1~9.2% (n = 3), 서로 다른 fiber들에 대하여서는 5.9~13.5% (n = 5)의 오차를 보였다. 도출된 분석조건을 이용하여 매립지 가스 중 BTEX를 포함한 35여종의 VOCs를 성공적으로 정량분석하였다.