• 한국지하수토양환경학회지:지하수토양환경
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• 제10권5호
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• pp.61-69
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• 2005

다양한 pH 조건하에서 휴믹물질 흡착적 분획현상에 의해 변화하는 용존 및 kaolinite에 흡착된 휴믹물질(Aldrich 휴믹산)과의 pyrene의 결합변화를 조사하였다. 먼저 흡착효과를 배제한 흡착 전 상태에서 bulk 휴믹산은, pH에 따른 분배(partitioning)과 크기별 배제효과 영향 차이에 의해 유기탄소 결합계수의 변화를 보였다. 모든 용액 pH 조건에 서 Aldrich 휴믹산은 kaolinite에 흡착하는 과정에서 분자량별 분획이 일어났으며 용존 휴믹산의 분자량은 흡착전의 분자량과는 달랐다. 그에 따라 흡착 후 남은 휴믹산과의 pyrene 결합계수는 흡착 전의 경우와 달랐다. pH 7과 9 조건에서 흡착 후 남은 휴믹산은 그 분자량과 pyrene 결합계수 사이에 양성 상관관계를 보였으나 그러한 상관관계가 pH 4의 조건하에서는 관찰되지 않았다. 이러한 차이는 흡착적 분획과정에서 pH 4인 경우 고분자에 대한 독점적 분획현상이 없었고 분자량에 대해 다소 균일한 분획이 일어났다는 점으로 설명할 수 있었다. 또한 관찰되는 분획현상 차이는 pH 조건에 따라 달라지는 흡착포화 정도 차이 때문인 것으로 사료된다. 흡착된 PAHA의 경우, 형태변화 (conformational changes) pyrene 결합에 중요한 것으로 나타났다. pH 7과 9 조건 하에서, 흡착전의 휴믹산의 경우 더 낮은 pyrene 결합계수를 보였고 이러한 형태변화효과는 pH가 높을수록 더 크게 나타났다.

• 대한환경공학회지
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• 제34권1호
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• pp.49-54
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• 2012

본 연구에서는 수 환경 내에서 일어나는 주요 자연분획변환 과정 중 생분해 시 변화하는 용존 유기물질의 특성이 중금속 결합특성에 미치는 영향을 조사하고자 하였다. 각각 호수와 하천 기원을 대표하는 Pony lake fulvic acid와 Suwannee river fulvic acid를 포함한 다양한 유기물을 대상으로 2주간 배양실험을 하여 변화하는 농도, 성상 및 중금속 구리 결합특성을 조사한 결과 각 시료 내 DOC농도는 감소하고 SUVA 값은 증가하였다. 특히 포도당 및 단백질계 탄소구조 함유비율이 높을수록 미생물에 의한 DOC 농도 분해율은 증가하였다. 포도당과 휴믹물질의 혼합비를 고려한 경우 배양 후 예측되는 혼합액의 DOC 감소율은 실제 측정값과 유사하였다. 그러나 SUVA값은 오히려 더 높게 나타나 생분해성 물질과 휴믹물질이 혼재할 경우 탄소 구조 변화로 인한 휴믹화의 진행이 더 크게 나타날 수 있음을 보였다. Synchronous 형광스펙트럼 결과 배양 후 Pony lake fulvic acid의 경우 휴믹산계 형광특성이, Suwannee river fulvic acid에서는 펄빅산계 형광특성이 크게 증가하였다. 포도당 시료에서는 배양 전 관찰되지 않았던 단백질계와 펄빅산계 형광특성이 관찰되었다. 중금속 구리와의 결합정도를 나타내는 log K 값은 미생물 배양 전과 후 휴믹물질 종류에 따라 변화가 없거나 혹은 약간 감소하는 경향을 나타냈다. 본 실험 결과는 미생물에 의한 휴믹물질 관련 형광구조의 증가가 중금속 결합력 강화에 영향을 미치지 않거나 오히려 감소시키는 것으로 보인다.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2004년도 총회 및 춘계학술발표회
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• pp.135-138
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• 2004

본 연구는 중금속으로 오염된 폐수처리에 있어 친환경적 유기흡착제로서 휴믹물질의 활용성을 평가하기 위한 기초 연구로서 이탄(peat moss)으로부터 Humin을 분리 한 후, 중금속 이온(Cd(II),Cu(II))과의 흡착특성을 조사하였다. 이탄으로부터 추출한 peat-Humin의 함량은 94%이상을 나타냈으며, 분자의 작용기 특성은 일반 토양 휴믹물질(soil humic substance)과 유사하였다. peat-Humin과 중금속 이온(Cd(II),Cu(II))과의 흡착 반응은 5분내에 빠른 흡착형을 보였으며, pH 5-6에서 가장 높은 중금속 제거율을 보였다. pH 3의 산성조건에서도 50%정도의 제거율을 보였다. pH 5에서의 등온흡착 실험결과를 Freundlich 등온식에 적용하여 해석한 결과, 각의 중금속에 대한 peat-Humin의 흡착상수(Kf)는 Cd(II)이 8.07 그리고 Cu(II)가 4.56으로 나타났다.

• 한국환경과학회지
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• 제19권3호
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• pp.261-267
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• 2010

The variation of assimilable organic carbon(AOC) concentration at each condition of ozonation was investigated using a model water and drinking water resource. AOC concentration of model raw water and drinking water resource tended to increase at low ozone dose. The maximum AOC concentration was detected when the residual ozone begin to be measured. Also, the AOC concentration increase at pH 8 compared to both pH 6 and 7 while that for pH 9 decreased rapidly. The removal characteristics of trihalomethane formation potential(THMFP) by ozonation was also investigated. Unlike the trend of AOC, the THMFP concentration never increased by ozonation but decreased even at low ozone dosage. From these results, the ozone dosage would be effective to simultaneously decrease both AOC and THMFP.

• 한국환경보건학회지
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• 제19권4호
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• pp.25-32
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• 1993

Granular activated carbon is commonly used in fixed-bed adsorbers to remove organic chemicals. In this experiment organic chemical solutions were prepared by adding the reagent grade organic chemical to distilled water. Isotherm adsorption tests of volatile organic chemicals were conducted using bottle-point technique and column test. Organic chemicals after passing through the column were extracted with hexane and analyzed with gas chromatography (Hewlett-Packard 5890) to check the adsorption capacity and breakthrough curve. The result were as follows: 1. The BET surface area of coconut activated carbon was 658~1,010 m$^2$/g where as coconut shell carbon was 6.6 m$^2$/g. Coconut activated carbon increased the BET surface area and adsorption capacity in bottle-point isotherm. 2. The adsorption capacity of coconut activated carbon for trichloroethylene (TCE) was reduced in the presence of humic substance. 3. A decrease in particle size of activated carbon resulted in higher adsorption capacity and lower intraparticle diffusion coefficient. It is reflected not only as a decrease in Freudlich adsorption capacity value (K) but also as an increase in Freudlich exponenent value (1/n).

• 한국물환경학회지
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• 제24권6호
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• pp.682-689
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• 2008

The purpose of this study was to find out the variation between molecular size distribution (MSD) of natural organic matter (NOM) in raw waters after different water treatment processes like conventional process (coagulation, flocculation, filtration) followed by advanced oxidation process (ozonation, GAC adsorption). The MSD of NOM of Suji pilot plant were determined by Liquid Chromatography-Organic Carbon Detection (LC-OCD) which is a kine of high-performance size-exclusion chromatography (HPSEC) with nondispersive infrared (NDIR) detector and $UV_{254}$ detector. Five distinct fractions were generally separated from water samples with the Toyopearl HW-50S column, using 28 mmol phosphate buffer at pH 6.58 as an eluent. Large and intermediate humic fractions were the most dominant fractions in surface water. High molecular weight (HMW) matter was clearly easier to remove in coagulation and clarification than low molecular weight (LMW) matter. Water treatment processes removed the two largest fractions almost completely shifting the MSD towards smaller molecular size in DW. No more distinct variation of MSD was observed by ozone process after sand filtration but the SUVA value were obviously reduced during increase of the ozone doses. UVD results and HS-Diagram demonstrate that ozone induce not the variation of molecular size of humic substance but change the bond structure from aromatic rings or double bonds to single bond. Granular activated carbon (GAC) filtration removed 8~9% of organic compounds and showed better adsorption property for small MSD than large one.

• 상하수도학회지
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• 제27권5호
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• pp.631-639
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• 2013

국내 하수처리장 인 방류기준이 강화되어 다양한 방법의 인 제거기술이 적용되고 있다. 흡착은 비교적 간단하면서 효과적으로 인을 제거할 수 있다. 본 연구에서는 흡착제인 Fe-Mn-Si oxide와 Fe-Mn oxide을 개발하여, 인 제거효율을 검토하였으며 이 흡착제에 대하여 Kinetic과 Isotherm모델을 비교하였다. 두 흡착제의 최대흡착양은 각각 47.8, 35.5 mg-$PO{_4}^{3-}/g$이었고, 이들은 낮은 pH에서 효과적으로 흡착하였다. Freundlish isotherm 모델이 Langmuir 모델보다 Fe-Mn-Si oxide의 흡착에 더 적합했다. 이온성 용액은 인이 흡착되는 과정에서 음이온들과 경쟁관계로 흡착능이 감소되었다. 비록 음이온과 humic물질들로부터 흡착에 영향을 받지만 Fe-Mn-Si oxide는 Fe-Mn oxide보다 흡착능이 크게 나타났다.

• 한국환경과학회지
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• 제6권6호
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• pp.595-604
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• 1997

To investigate characteristics of biogeochemical environment of the Korea Deep Ocean Study(KODOSI area in the northeast Pacific Ocean, we preferentially measured Inorganic nutrients and fluorescent organic matters. Typically. the permanent thermocline was well developed at the depth of 200~1000m In the study area. Nitrate. phosphate and silicate were low In the surface mixed layer and Increased with depth. N/P and N/Si showed 15 and 0.2 respectively In the deeper layer. Two fluorophores, biomacromolecule(protein-like) and geomacromolecule (humid-like) , were observed by three dimensional fluorescence excltatlon/ emission spectra matrix. Biomacromolecule(maximum fluorescence at $Ex_{280m}/Em_{330nm}$) ranged from 41.9 to 147.0 TU with its maximum In the surface mixed layer and minimum in deeper water, This is a same trend that has been reported for DOC in the equatorial Pacific. This suggests that biomacromolecule might be labile and converted to refractory humic substance after bacterial degradation In the deeper layer. On the contrary, geomacromolecule(maximum fluorescence at $Ex_{330m}/Em_{430m}$), ranged from 7.6 to 46.5 QSU, showed minimum in the surface nixed layer(euphotic zone) Implying photodegradation and then increased with depth at all stations. In the characteristics of vertical profiles, the relationship between biomacromolecule and geomacromolecule showed negative correlation. Such trend can be attributed to biochemical regeneration or formation of fluorescent materials accompanying oxidation and rennnerallzation of settling organic matter.

• The Plant Pathology Journal
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• 제16권4호
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• pp.189-199
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• 2000

To search for the antifungal substances, various actino-mycete isolates were obtained from various soils of Korea using plate dilution method on the humic acid vitamin agar plates. In the screening procedures using a dual culture method, 32 actionomycete isolates were selected, which showed the inhibitory activity against mycelial growth of plant pathogenic fungi Altirnaria mali, Colletotrichum gloeosporides, Fusarium oxysporum f.sp. cucumerinum, Magnaporthe grisea, Phytophthora capsici, and Rhizoctonia solani. Bioassay of the crude extracts from culture filtrates and mycelial mets revealed that 12 antagonistic actionomycetes produced highly active antifungal substances. Actinomycete strain S5-55 which showed the substantial antifungal activity against the tested fungi was selected for production of the antifungal substances. Based on the cytochemical and morphological characteristics, strain S5-55 was identified as a Streptomyces species. The results of the numerical identification using the TAXON program confirmed that Streptomyces strain S5-55 was identical with Streptomyces humidus including in TAXON major cluster 19. The production of antifungal substance was most favorable when S. humidus strain S5-55 was cultivated for 10 dats on soluble starch broth supplemented with $K_2$HPO$_4$. The antifungal substances active against the plant pathogenic fungi P. capsici and M. grisea were partially purified using $\textrm{C}_{18}$ reversed-phase column chromatography.

• 상하수도학회지
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• 제11권1호
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• pp.81-87
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• 1997

Coagulation is very important process in water works. The subsequent processes are directly affected by this process. Many factors such as turbidity, alkalinity, pH, hardness, total organic carbon(TOC), velocity gradient and flocculation time effect on coagulation process. Among these factors, specially TOC is being concerned target substance to be removed due to trihalomenthanes(THMs) precursor and alkalinity is being one of the major parameter for removing TOC. We have researched the consumption of coagulant with TOC alkalinity concentration of water and removal efficiency of residual TOC and turbidity with alkalinity. Furthermore we have investigated particle size distributions with velocity gradient and alkalinity. The consumption of coagulant was proportionally increased to TOC and alkalinity concentration and the removal of TOC in Nakdong river water was very difficult more than 150 mg/l in alkalinity but large morecular weight organic such as humic acid could be removed easily. Coagulation of low alkalinity water was more rapidly occured than of high alkalinity water by analyzing the particle size distributions. High alkalinity water needed higher mixing energy for a good coagulation within limited flocculation time.