• 한국환경보건학회지
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• 제32권6호
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• pp.543-555
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• 2006

During a twenty-day period in 2005, a nine-stage Andersen cascade impactor was used to determine the seasonal size distribution of atmospheric particles and its inorganic ion species sampled for 24hr in Iksan city, located southwest of the Korean peninsula. Samples were analyzed for major water-soluble ion species using Dionex-100 ion chromatograph. Average fine and coarse mass concentrations of atmospheric particles were, respectively, 31.4 and $82.6{\mu}g\;m^{-3}$ in spring and 35.8 and $73.4{\mu}g\;m^{-3}$ in fall-winter during the sampling period of 2005, while measurements of 69.8 and 9.9 were obtained in the sampling period of summer, The size distribution of particulate mass concentration during the non-Asian dust period was generally bimodal, whereas the size distribution of particulate mass concentration during the Asian dust period was unimodal due to the significant increase of coarse particles, which originated from long-range transport of soil dust particles from loess regions of the Asian continent. Among ionic species, $SO{_4}^{2-},\;NH{_4}^+,\;K^+$ were mainly distributed in fine particles due to their characteristics of emission sources and gas-to-particle conversion, while $Na^+,\;Mg^{2+}\;and\;Ca^{2+}$ were dominantly in coarse particles. However, $NO_3{^-}\;and\;Cl^-$ were distributed in both coarse particles and fine particles. Although $SO{_4}^{2-}$ was mainly distributed in fine particles, the size distributions of $SO{_4}^{2-}$ in coarse mode were significantly increased during the Asian dust events compared to those during the non-Asian dust period. $Ca^{2+}$ showed the most abundant species in the atmospheric particles during the Asian dust period. $NH{_4}^+$ was found to mainly exist as $(NH_4)_2SO_4$ in fine particles.

• 한국대기환경학회지
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• 제11권2호
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• pp.179-184
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• 1995

This study was carried out to characterize sources of suspended particulate matter(SPM) in Mt. Soback area from January to Novembver in 1993. The collection and major water soluble ion analysis of SPM were conducted by using a High Volumn Air Sampler(HVAS; W&A Inc., PM-10) and ion chromatograph(DIONEX 4000i), respectively. The variations of SPM and major ion concentrations were found to be 9. sim. 156.mu.g/ $m^{3}$, $F^{-10}$ 0.00 .sim. 0.15.mu.g/ $m^{3}$, C $l^{-10}$ 0.06 .sim. 3.79.mu.g/ $m^{3}$, N $O_{3}$$^{-10}$ 0.90 .sim. 6.85.mu.g/ $m^{3}$, S $O_{4}$$^{2-}$ 1.99 .sim. 9.36.mu.g/ $m^{3}$ N $a^{+}$0.00 .sim. 0.27.mu.g/ $m^{3}$, N $H_{4}$ $^{+}$0.72 .sim. 5.77.mu.g/ $m^{3}$, $k^{+}$0.03 .sim. 0.88.mu.g/ $m^{3}$ and $Ca^{2+}$0.12 .sim. 2.76.mu.g/ $m^{3}$. Tree sources were identified by Principal Component Amalysis(PCA) using a SPSS/P $C^{+}$. The explanation ability of forst, second and third Principal Component were 60.8%, 13.6%, 8.2%, of total variance. The sources classfied by PCA were found to be secondary aerosol/fuel combustion, soil dust related cement production/yellow sand and aerosol related waste burning.related waste burning.g.

• Archives of Pharmacal Research
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• 제28권10호
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• pp.1190-1195
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• 2005

The objective of this study was to develop an assay for mequitazine (MQZ) for the study of the bioavailability of the drug in human subjects. Using one mL of human plasma, the pH of the sample was adjusted and MQZ in the aqueous phase extracted with hexane; the organic layer was then evaporated to dryness, reconstituted and an aliquot introduced to a gas chromatograph/mass spectrometer (GC/MS) system with ion-trap detector. Inter- and intra-day precision of the assay were less than 15.1 and $17.7{\%}$, respectively; Inter- and intra-day accuracy were less than 8.91 and $18.6{\%}$, respectively. The limit of quantification for the current assay was set at 1 ng/mL. To determine whether the current assay is applicable in a pharmacokinetic study for MQZ in human, oral formulation containing 10 mg MQZ was administered to healthy male subjects and blood samples collected. The current assay was able to quantify MQZ levels in most of the samples. The maximum concentration ($C_{max}$ was 8.5 ng/mL, which was obtained at 10.1 h, with mean half-life of approximately 45.5 h. Under the current sampling protocol, the ratio of $AUC_{t{\rightarrow}last}$ to $AUC_{t{\rightarrow}{\infty}}$ was $934{\%}$, indicating that the blood collection time of 216 h is reasonable for MQZ. Therefore, these observations indicate that an assay for MQZ in human plasma is developed by using GC/MS with ion-trap detector and validated for the study of pharmacokinetics of single oral dose of 10 mg MQZ, and that the current study design for the bioavailability study is adequate for the drug.

• 공업화학
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• 제10권1호
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• pp.30-34
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• 1999

클로로타노닐과 엔도슬판을 UV 조사, pH 3.0에서의 UV조사, 그리고 3.5% 염수에서 UV조사를 하여 광분해 거동을 연구하였다. 농약의 광분해과정은 가스크로마토그래프, 총유기탄소, 그리고 이온크로마토그래프를 사용하였다. Low pressure mercury multilamp($8W{\times}6$)를 반응기에 잠수시켜 실험을 하였으며, 초기농도는 10 ppm으로 하였다. 클로로타노닐은 UV 조사, pH 3.0조건에서 UV조사, 그리고 3.5% 염수조건에서 UV조사 조건에서 반응시간 30분에 거의 광분해되었다. 자외선조사에서 엔도슬판-${\alpha}$는 38%, 엔도슬판-${\beta}$는 25% 분해되었다. 엔도슬판-${\alpha}$(83%)는 자외선조사에서 65%, pH 3.0의 자외선조사에서 70%, 35% 염수의 자외선조사에서는 75% 분해되었다. 엔도슬판(16%)는 자외선조사에서 80%, pH 3.0의 자외선조사에서는 98%, 3.5% 염수의 자외선조사에서는 90% 분해되었다.

• 분석과학
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• 제16권2호
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• pp.110-116
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• 2003

사용 후 핵연료의 화학특성 연구를 위하여 요오드의 분리와 정량에 관한 연구를 수행하였다. 사용 후 핵연료를 용해시키는 과정에서 핵연료 중에 CsI로 존재하는 요오드가 $I_2$로 산화되어 휘발되지 않도록 질산과 염산의 혼합산 (80:20 mol%)을 이용하여 비휘발성 ${IO_3}^-$­로 안정화시켰다. 2.5 M $HNO_3$ 매질에서 $NH_2OH{\cdot}HCl$을 이용하여 $I_2$로 환원시킨 후 사염화탄소로 추출하여 우라늄과 핵분열생성물로부터 분리, 회수하였다. 0.1 M $NaHSO_3$을 사용하여 요오드를 역추출하였으며 수용액층으로 회수된 요오드를 이온 크로마토그래피로 정량하였다. 방사성 물질 분석에 적합한 이온 크로마토그래피/차폐 시스템을 구성하였으며 42,000~44,000 MWd/MtU 의 연소도를 갖는 사용후핵연료를 대상으로 요오드를 분석한 결과 Origin 2 연소도 전산코드에 의한 계산결과인 $324.5{\sim}343.6{\mu}g/g$와는 -8.3~-0.5%의 편차를 나타내었다.

• 한국식품위생안전성학회지
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• 제13권3호
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• pp.252-257
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• 1998

죽염은 예로부터 위궤양 등의 소화기 질환에 민간요법으로 사용되어 왔으며 대나무 통속에 천일염을 넣고 소나무 장작불로 9번 구워서 만들어진다. 본 연구에서는 죽염의 특성분석시험과 항위궤양 시험 중 위산분비 억제도 시험을 실시하였다. 특성분석시험으로 ICP(Inductively Coupled Plasma) spectrometer, IC(Ion Chromatograph), XRD(X-ray Diffractrometer), 전자현미경을 이용하여 천일염과 죽염제품 A, B, C의 성분 및 구조분석을 실시하였다. 그 결과, 성분분석시험에서 죽염은 천일염에 비하여 칼륨, 규소, 철 및 인삼염의 농도가 증가하였으며 황산염은 감소되었음을 알 수 있었다. 죽염 중 물불용분에 포함된 화합물은 MgO가 가장 많았고, $SiO_2,\;Mg_2Si_O4\;및\;CaMgSiO_4$등도 확인되었다. 구조분석에서 죽염은 천일염에 비하여 대체로 표면이 매끄럽고 용융되어 있는 것으로 나타났다. 죽염제품 A, B, C 중 A를 사용하여 위산분비에 미치는 영향을 측정하였다. SD계 랫드에 죽염, 천일염, 시약급 NaCl, 증류수를 1일 1회 28일 동안 각 0.2, 1.0, 2.0 g/kg으로 경구 투여하여 마지막 투여 후 24시간 절식시켜 Shay 유문 결찰법을 이용하여 채취한 위액의 총량, pH, 총위산도, 펩신활성도를 측정하였다. 실험결과 각 투여 용량군에서 용매 대조군에 비하여 통계학적으로 유의성 있는 차이를 나타내지 않았으며 죽염을 포함한 여러 가지 염투여는 위산분비에 영향을 주지 않았다. 따라서 28일간 죽염투여에 의한 위궤양 치료효과는 기대하기 어려울 것으로 사료된다.

• 분석과학
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• 제23권2호
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• pp.155-160
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• 2010

먹는 물 중 bromate의 국내 외 시험방법에 대한 분석 조건을 비교하여 최적 시험조건을 확인하고 ion chromatograph-suppressed conductivity detector (IC-CD)를 사용하여 먹는 샘물 중 bromate 함량을 분석하였다. 시료 전처리를 위해 먹는 샘물 20 mL를 온가드 Ba-, Ag-, H-카트리지 순서대로 통과시키고 마지막에 $0.2\;{\mu}m$ 맴브레인 필터로 여과 하였다. 여과한 시료는 IC-CD에 주입하였으며, 시료 중 bromate는 10~50 mM의 KOH 이동상 및 수산화이온용액 이동상에 적합한 가드 및 분석용 컬럼인 AG 19 및 AS 19에 의해 분리하였다. Bromate의 검정 곡선은 $0.5\sim40\;{\mu}g/L$의 농도 범위에서 $r^2$값이 0.9998로 좋은 직선성을 보였으며, 방법검출한계(MDL) 및 정량한계(LOQ)는 각각 0.1, $0.5\;{\mu}g/L$이었다. 2009년 9월 이후 유통 중인 먹는 샘물 157 개 시료를 분석한 결과, 33 개 시료에서 bromate가 검출되었으며, 검출된 시료의 평균농도는 $2.4\;{\mu}g/L$ 이었다. 측정 농도 범위는 $0.5\sim6.5\;{\mu}g/L$로 모두 국내 먹는샘물 수질기준인 $10\;{\mu}g/L$ 이내였다.

• Journal of Preventive Medicine and Public Health
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• 제18권1호
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• pp.59-71
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• 1985

During a period from February 1st to November 30th in 1983, measurements were made twice a month on dustfalls and concentrations of various cations ana anions in their filtrates in an urban (Heuksuk-dong, Seoul) and in a rural (Ansung) districts. Standard British Deposit Gauge method was applied for collection of dustfalls and ion chromatographic method using Ion Chromatograph 10 (Dionex, U.S.A.) for determination of cation and anion concentrations. The results obtained were as follows: 1. Annual mean values of dustfalls were $8.30{\pm}5.09tons/km^2/month$ in an urban and $6.20{\pm}0.82tons/km^2/month$ in a rural districts. And annual mean values of pH of filtrates of the collected samples were $5.3{\pm}0.76$ in an urban and $6.0{\pm}0.82$ in a rural districts. 2. Annual mean concentrations of common cations and anions in their filtrates were as follows: urban rural (unit: ppm) $$Na^{+}\;1.7{\pm}1.30\;1.9{\pm}1.86$$ $$NH^{+}_{4}\;2.4{\pm}1.60\;1.3{\pm}1.59$$ $$K^{+}\;0.7{\pm}0.47\;1.5{\pm}3.79$$ $$Ca^{++}\;5.3{\pm}0.95\;3.4{\pm}2.58$$ $$Mg^{++}\;0.7{\pm}0.89\;0.5{\pm}0.83$$ $$Cl^{-}\;2.0{\pm}1.31\;4.0{\pm}2.35$$ $$NO^{-}_{3}\;4.0{\pm}2.35\;2.7{\pm}1.31$$ $$So^{--}_{4}\;16.9{\pm}17.40\;6.8{\pm}8.00$$ Some of anions such as $Br^{-},\;{PO_4}^{-3}\;and\;{NO_2}^{-}$ were scarecely detected and $F^{-}$ was measured at very low concentrations ranging from 0.1 to 0.5 ppm in Feb., Oct. and Nov. in an urban and in Feb. in a rural districts. 3. By two-way analysis of variance with 4 replications for dustfalls, pH and concentrations of various ion by district and month of a year, statistically significant differences were noted in dustfalls (p<0.01), pH (p<0.01) and concentrations of various ion (p<0.01) by month of a year, and in dustfalls (p<0.05) and concentrations of various ion such as ${NH_4}^{+},\;Ca^{++},\;{NO_{3}}^{-}\;and\;{SO_4}^{--}$ (p<0.01) by district. 4. There were statistically significant differences pH in Spring (Feb., Mar and Apr.) (p<0.01) and in ${SO_4}^{--}$ in Autumn (Aug., Sept., Oct. and Nov.) (p<0.05) between the two districts.

• 한국환경농학회지
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• 제36권4호
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• pp.288-292
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• 2017

BACKGROUND: Silicon tetrachloride reacts with moisture in the atmosphere to generate hydrogen chloride, which affects the environment. Since silicon tetrachloride and its by-products are dispersed in the atmosphere in a short time after the silicon tetrachloride release into the atmosphere, it is difficult to directly assess the extent of environmental impact. In the present study, the exposure test of silicon tetrachloride or hydrogen chloride was examined in order to establish the criterion of the range affected by the silicon tetrachloride release, and the actual crops in the area exposed to silicon tetrachloride leakage were analyzed. METHODS AND RESULTS: For the experiment of exposure to silicon tetrachloride or hydrogen chloride, the leaves of red-pepper and corn were used in glass sealed containers. In the actual accident area, 59 samples from 10 different kinds of crops were collected. The pretreatment of the sample was performed by freezing and grinding, and then extracted using distilled water. The pH and concentration of chloride ($Cl^-$) ion of the extracted solution were measured using pH meter and ion chromatograph, respectively. CONCLUSION: Exposure to silicon tetrachloride caused visible damage, increasing the concentration of chloride ion, and decreasing the pH as well as hydrochloric acid. In the actual crops of the affected area, the tendency was the same as the result of the laboratory test, and the range of influence could be estimated through the concentration of $Cl^-$ ion over 2,000 mg/kg, and the correlation evaluation between the concentration of $Cl^-$ and pH. Therefore, the concentration of $Cl^-$ ion and the correlation between $Cl^-$ and pH would be considered as the factors to estimate the influence range of silicon tetrachloride release.

• 방사성폐기물학회지
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• 제7권1호
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• pp.17-23
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• 2009

방사성 액체폐기물에 함유되어 있는 우라늄의 추출제 또는 아미드 (amide) 화합물 추출제를 사용한 용매추출계에서 제 3상 생성 방지제로 사용되는 dihexyloctanamide(DHOA)을 합성하고, 이를 $^{60}Co$ 감마 방사선으로 조사시킬 때 생성된 방사선 분해생성물 (radiolysis product)을 정량 분석하였다. 방사선 조사된 DHOA에 대한 FT-IR 스펙트럼과 방사선 분해생성물에 대한 GC/MS 스펙트럼 그리고 GC/MS-SIM 방법으로 측정한 결과를 근거로 octanoic acid와 dihexylamine 2종의 방사선 분해생성물의 존재를 확인하였으며, 이들 2종 화합물의 표준시약과 tridecane을 내부표준물질(ISTD)로 사용하여 GC/MS-SIM 방법으로 정량 분석하였다. 방사선 분해생성물에 대한 총 이온 크로마토그램에서 나타난 머무름 거동, 분리도 및 해 상도에서 정량 분석할 수 있는 결과를 얻었으며, 총 이온 크로마토그램에서 분리피크가 나타나는 시간은 octanoic acid는 8.65분, tridecane은 9.79분 그리고 dihexylamine은 10.27분이었다. 그리고 DHOA의 방사선 흡수선량이 증가할수록 octanoic acid의 농도는 감소하였으며, dihexylamine의 농도는 증가하였다.