• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2002년도 추계학술발표회
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• pp.191-194
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• 2002

Humic acid, fulvic acid and humin present in volcanic ash soil were isolated by IHSS standard procedure and their characteristics were analyzed as a basic study to evaluate the effect of humic substances on the behaviour of pollutants in contaminated surface soil. The volcanic ash soil contained 42.1 % of total organic matter based on the oven-dried soil, and humin, humic and fulvic acids corresponded to 67.5 %, 15.2 %, 7.6 % of TOM respectively. Structural informations of the humic fractions were obtained from their elemental analysis and IR, CPMAS C-13 NMR spectral analysis and the differences among them are discussed with their C/H, O/C ratios and distributions of carbon types in the molecules.

• 산업기술연구
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• 제27권B호
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• pp.109-114
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• 2007

Humic substances generally comprise 30-50% of the dissolved organic carbon in water. They can affect water quality adversely in several ways and they are important from a water treatment perspective due to their role as precursors for the formation of chlorination by-products such as trihalomethanes. The objectives of this research are to investigate the characteristics of organic matter using raw water of Chuncheon area, to isolate the humic substance fractions from natural water samples, and characterize the extracted humic substances. Humic substances were fractionated according to "isolation of IHSS aquatic humic and fulvic acids" using XAD resin adsorption technique. Characteristics of humic substances were analyzed through DOC, $UV_{254}$, $SUVA_{254}$, FT-IR spectra, fluorescence analysis.

• 분석과학
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• 제17권2호
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• pp.163-172
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• 2004

토양 풀빅산 (FA)의 분자량 크기 분포와 분자량별 형광특성을 겔 여과 크로마토그래피(GFC)와 형광분석시스템을 사용하여 분석하였다. 본 연구에서는 제주 지역 토양에서 추출한 풀빅산을 세 개의 분자량 영역으로 분리하였고, 분자량별 풀빅산의 excitation, emission, synchronous 형광특성을 비교 분석하였다. 토양 풀빅산의 분자량 분리를 위한 GFC 시스템은 아세톤과 덱스트란 블루 및 폴리에틸렌 글리콜 표준분자를 사용하여 교정하였다. 분자량 분리 시스템의 틈새부피는 130 mL이고, total permeation volume은 404 mL을 나타냈다. 이 시스템을 풀빅산의 분자량 분리에 적용한 결과, 토양 풀빅산은 190~8,900 Da의 분자량 분포를 나타냈으며 피크점에서의 분자량은 930 Da을 나타냈다. 분자량별 구조 차이를 나타내는 synchronous 형광피크의 상대비 ($I_{498nm}/I_{390nm}$)는 분자량이 클수록 증가하였다. 이와 같은 결과는 고 분자량의 풀빅산이 저 분자량의 풀빅산에 비해 ${\pi}$-결합으로 연결된 방향족 고리와 다양한 치환기가 결합된 좀더 복잡한 분자 구조임을 제시한다.

• 대한환경공학회지
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• 제22권7호
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• pp.1253-1261
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• 2000

천연유기물질은 지표수와 지하수내 탁도를 유발하고 humic (humic acid와 fulvic acid)과 nonhumic 성분으로 구성된다. 일반적으로 NOM은 소독부산물(DBP) 전구물질로써 수처리시 관심의 대상이 된다. 원수의 특성은 정수공정의 선택과 적용에 중요한 정보를 제공한다. 수원에 따른 NOM의 상당한 차이가 다양한 원수들 사이에서 관찰되었고, 문제시되는 NOM을 제거하고 전환시키기 위한 목적으로 정수공정을 적용한다. 본 연구의 결과, 산화처리에 의해 전체 DOC 농도의 변화는 거의 없었지만, 고분자의 소수성 물질이 저분자의 친수성 물질로 전환되었고, 염소보다 오존의 경우 그 산화력의 차이 때문에 SUVA 값의 감소가 더 크게 나타났다. 응집처리에 의해 hydrophilic 성분보다 분자량이 더 큰 hydrophobic 성분이 응집 침전되어 훨씬 잘 제거되었다. THMFP는 50% 정도까지 제거되었는데, 이것은 상대적으로 THMFP를 잘 유발시킨다는 humic acid 성분의 제거가 원활하게 일어났기 때문이다.

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1997년도 춘계학술발표회논문집(2)
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• pp.439-444
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• 1997

In order to investigate organic association of fallout cesium, strontium and plutonium in the soil, soil samples influenced by fallout from nuclear weapon testings were treated with alkali (0.1 M-sodium hydroxide solution) to extract organic acids. After extraction, the resultant three fractions (sedimentary residue, humic and fulvic acid fractions) were subjected to the r-ray spectrometric analysis for $^{137}$ Cs, and radiochemical analysis for gosr and $^{239,240}$Pu. Alkali extraction experiments showed that a lot of $^{ 239,240}$Pu was extracted to organic acids from the soil samples, whereas most of $^{137}$ Cs and $^{90}$ Sr remained in residual fraction. Less than 10% of the total $^{137}$ Cs and $^{90}$ Sr was found in the organic fraction. The concentrations of $^{137}$ Cs and $^{90}$ Sr associated with humic fractions were higher than those with the corresponding fulvic fractions. It was found that more than 40% of the total $^{239,240}$Pu was associated with the organic fraction of soils. In contrast with $^{137}$ Cs and $^{90}$ Sr, $^{239,240}$Pu associated with vulvic fractions was much higher than in humic fractions.

• Environmental Engineering Research
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• 제7권2호
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• pp.93-101
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• 2002

The seasonal patterns of dissolved organic matter (DOM) in Lake Kasumigaura, a shallow, eutrophic lake, and serveral DOM sources in its catchment area were investigated. DOM was fractionated using three resin adsorbents into classes: aquatic humic substances (AHS=humic acid+fulvic acid), hydrophobic neutrals (HoN), hydrophilic acids (HiA), bases (BaS) and hydrophilic neutrals (HiN). The DOM produced significantly different fraction distributions depending on the origin of sample. AHS and HiA prevailed over AHS in the lake while AHS and HiA existed at almost the same concentration levels in the rivers. AHS seems to be a more dominant component in rever water than lake water. The dominance of organic acids was also observed in the DOM sources: forest stream (FS), plowed field percolate (PFP), domestic sewage (DS) and sewage treatment plant effluent (STPE).

• 한국환경농학회지
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• 제11권3호
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• pp.235-242
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• 1992

부식산과 흘브산이 Paraquat의 약해에 미치는 영향은 호밀의 생물검정을 통해 고사일수, 생중량 및 성장률에 관한 약해지표를 설정하고 Model을 도입하여 평가했다. 호밀의 생육상황에 대한 유기리간드 자체의 영향은 거의 없었으나, Paraquat의 독성은 매우 높았다. Paraquat의 약해가 강하게 나타나기 시작하는 농도는 $0.4{\sim}0.6{\mu}M$ 이었으며, 약해한계농도 (Phytotoxic Critical concentration)는 약 11${\mu}M$ 로 추정되었다. 유기리간드의 처리는 Paraquat의 약해에 의해 초래되는 고사일수를 약 40%까지 지연 시켰으며, Paraquat 단독처리구보다 생중량 및 성장률을 유의성있게 향상시켜, Paraquat의 호밀에 대한 약해를 줄여 주었다.

• 대한환경공학회지
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• 제35권11호
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• pp.769-775
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• 2013

본 연구에서는 두 가지 기원의 표준 휴믹물질 혼합 시료와 Suwannee River fulvic acid (SRFA)을 사용하여 광분해로 인한 용존 유기물질의 스펙트럼 특성 변화와 이에 따른 소독 부산물 생성능의 변화를 조사하였다. 혼합시료의 염소소독부산물 발생잠재력(DBPFP)은 specific UV absorbance (SUVA) 값에 비례하여 증가하였다. 7일간 광분해 후 혼합시료의 SUVA 값은 모두 감소하였다. 그러나 동일 시료에서 DBPFP 값은 SUVA 감소폭보다 적었다. 비록 두 변수 사이에 직선성은 유지되었으나 같은 SUVA 범위 내에서의 DBPFP 값은 오히려 감소하는 경향을 보였다. 이 결과는 광분해로 인해 염소소독부산물 전구체 역할을 하는 비방향족 물질이 생성될 수 있음을 시사하였다. SRFA 시료에 대해 4일과 13일 광분해하여 각각 저분자와 고분자 부분에서의 DBPFP 값을 비교한 결과 광분해 후 유기탄소 당 염소소독부산물 발생량 변화양상은 염소소독부산물 종류에 따라 다르게 나타났다. 유기탄소 당 trihalomethenes (THMs) 발생은 광분해 후 고분자 부분에서 더 높았으나 haloacetic acids(HAAs)의 경우 고분자와 저분자 부분 사이의 유의한 차이가 관찰되지 않았다. 광분해 시간에 따른 유기탄소 당 DBPFP 값 변화 패턴도 용존 유기물 분자량에 따라 다르게 나타났다. THMs의 경우 고분자 부분에서는 광분해 시간에 따라 증가하는 경향을 보였으나 저분자에서는 큰 변화를 보이지 않았다. 반면 HAAs은 고분자에서 지속적인 감소 경향을, 저분자 부분에서는 증가 후 다시 감소하는 경향을 보였다. 본 연구결과 수중 유기물질은 전반적으로 광분해에 따라 소독부산물 생성능이 초기에 오히려 증가할 수 있으며 광분해 시간이 충분히 지속된 후에야 감소함을 보여주었다.

• 한국대기환경학회지
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• 제27권3호
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• pp.337-346
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• 2011

24-hr integrated measurements of water-soluble organic carbon (WSOC) in PM2.5 were made between May 5 and September 25, 2010, on a six-day interval basis, at the Metropolitan Area Air Pollution Monitoring Supersite. A macro-porous XAD7HP resin was used to separate hydrophilic and hydrophobic WSOC. Compounds that penetrate the XAD7HP column are referred to hydrophilic WSOC, while those retained by the column are defined as hydrophobic WSOC. Laboratory calibrations using organic standards suggest that hydrophilic WSOC includes lowmolecular aliphatic dicarboxylic acids and carbonyls with less than 4 or 5 carbons, amines, and saccharides. While the hydrophobic WSOC is composed of compounds of aliphatic dicarboxylic acids with carbon numbers larger than 4~5, phenols, aromatic acids, cyclic acid, and humic-like Suwannee River fulvic acid. Over the entire study period, total WSOC accounted for on average 48% of OC, ranging from 32 to 65%, and hydrophilic WSOC accounted for on average 30.5% (9.3~66.7%) of the total WSOC. Based on the previous results, our measurement result suggests that significant amounts of hydrophobic WSOC during the study period were probably from primary combustion sources. However, on June 9 when 1-hr highest ozone concentration of 130 ppb was observed, WSOC to OC was 0.61, driven by increases in the hydrophilic WSOC. This result also suggests that processes, such as secondary organic aerosol formation, produce significant levels of hydrophilic WSOC compounds that add substantially to the fine particle fraction of the organic aerosol.

• Asian-Australasian Journal of Animal Sciences
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• 제28권2호
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• pp.215-222
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• 2015

The objective of this research was to evaluate the growth performance, the apparent ileal digestibility of nitrogen and energy, the retention of nutrients and the apparent metabolizable energy corrected to zero nitrogen retention (AMEn) in broiler chickens supplemented with increasing doses of a worm leachate (WL) as a source of humic substances (HS) in the drinking water. In Exp. 1, 140 male broilers were penned individually and assigned to four WL levels (0%, 10%, 20%, and 30%) mixed in the drinking water from 21 to 49 days of age. Water was offered in plastic bottles tied to the cage. In Exp. 2, 600 male broilers from 21 to 49 days of age housed in floor pens were assigned to three levels of WL (0%, 10%, and 20%) mixed in the drinking water. The WL was mixed with tap water in plastic containers connected by plastic tubing to bell drinkers. The results of both experiments were subjected to analysis of variance and polynomial contrasts. In Exp. 1, the daily water consumption was similar among treatments but the consumption of humic, fulvic, and total humic acids increased linearly (p<0.01) as the WL increased in the drinking water. The feed conversion (p<0.01) and the ileal digestibility of energy, the excretion of dry matter and energy, the retention of dry matter, ash and nitrogen and the AMEn showed quadratic responses (p<0.05) relative to the WL levels in drinking water. In Exp. 2, the increasing level of WL in the drinking water had quadratic effects on the final body weight, daily weight gain and feed conversion ratio (p<0.05). The addition of WL as a source of HS in the drinking water had beneficial effects on the growth performance, ileal digestibility of energy, the retention of nutrients as well on the AMEn in broiler chickens; the best results were observed when the WL was mixed at levels of 20% to 30% in the drinking water.