The objective of this study was to evaluate the immobilization of heavy metals (Cu, Pb, Zn and Cd) in an abandoned mine soil by applying both soluble phosphates and steel slag as stabilizers. The application rate of stabilizers to soils was determinated based on PO4/Pb molar ratio of 2.0 for phosphates and on weight/weight ratio of 2, 5, 10% for steel slag, respectively. Immobilization efficiency of heavy metals in the contaminated soils was evaluated by toxicity characteristics leaching procedure (TCLP). After adding both phosphate and slag, the immobilization efficiencies of Cu, Zn and Cd increased significantly (about 14% - 40%) compared to those of treatment with soluble phosphate alone. The increae in immobilization efficiencies of Cu was the greatest. Whereas, immobilization efficiency of Pb was not significantly different from those with soluble phosphate alone. Among the tested three phosphates (Na2HPO4 ·12H2O, Ca(H2PO4)2 ·H2O, (NH4)2HPO4), the immobilization efficiencies with Na2HPO4 ·12H2O increased more than those of other phosphates. Results of sequential extraction analysis indicated that fraction of reducible form (F3) and residual form (F5) increased, while mobile forms (F1, and F2) decreased after immobilization treatment with both stabilizers resulting in decrease in leachability of heavy meyals in the treated soils. Residual fraction of Cu after treatnment was the highest as 68.5%, it was followed by Cu > Pb > Zn > Cd.

한중콘크리트 공사에 적용을 검토할 수 있는 초속경 콘크리트는 초기 급속한 발열반응을 통해 동해를 입기 전에 소요의 강도를 확보할 수 있을 것이며, 열 보상을 통해 시공환경이 유지될 경우 강도발현에 필요한 시간을 단축할 수 있는 장점이 있다. 일반 콘크리트는 영하의 기온에서 타설할 경우 양호한 경화를 얻을 수 없으며, 저온에서 동해를 방지하고 경화성을 확보하기 위하여 내한방동제를 첨가하여 사용하고 있다. 그러나, 내한방동제의 대부분은 염화물을 주성분으로 하고 이를 다량으로 사용할 경우, 콘크리트의 동결을 방지하고 시멘트의 수화반응을 촉진시켜 응결시간을 단축하고 초기강도 증진을 유도하는 효과가 있는 반면, 장기재령에서 강도발현이 문제가 되고, 경제성이 떨어진다는 단점이 있다. 최근 연구되고 있는 마그네시아 인산염 복합체는 초속경성이 있고 저온에서도 수화반응이 가능한 것으로 보고되고 있어 새로운 한중공사 및 극한지용 건설재료로 사용할 수 있을 것으로 판단된다. 따라서, 본 연구에서는 한중공사 및 극한지에서 사용이 가능한 건설재료의 개발을 위한 사전 연구의 일환으로서, 마그네시아 인산염 복합체를 활용한 모르타르에 대해 온도의 영향을 고려한 재료 물성 평가를 실시하고 적정 배합을 제안하고자 한다.

The objective of this study was to evaluate the immobilization efficiency and sequential extraction of soluble phosphates (Na2HPO4 ·12H2O, Ca(H2PO4)2 ·H2O, (NH4)2HPO4) for the stabilization of heavy metals (Cu, Pb, Zn and Cd) in abandoned mine soil. The application rate of stabilizers to soils was determinated PO4/Pbtotal molar ratio of 0.5, 1.0, 2.0, 4.0. The immobilization efficiency was evaluate of TCLP (EPA method 1311) used in a landfill for heavy metals. After processing stabilization, the immobilization efficiency of Pb is more than 95% at molar ratio of 2.0 regardless kind of phosphate. For Cu Zn and Cd, on the other hand, the efficiency has the range of from 30% to 50%, even though molar ratio increase up to 4.0. It is relatively low in comparison with Pb. Leachability of heavy metals was reduced with increasing amounts of added phosphate. Phosphates, Na2HPO4 ·12H2O was more immobilization than Ca(H2PO4)2 ·H2O, (NH4)2HPO4. After sequential extraction, form of heavy metals in soil tends to increase strongly bond like forms of organic matter-bound(F4) and residual (F5). Especially the stable residual form increases in all metals. The growth rate of residual fraction was a little different heavy metals. The growth rate of Zn is greatest increased from 17% to 22% than other metals, it was followed by Zn > Cd > Pb > Cu. Phosphates, Ca(H2PO4)2 ·H2O was the greatest increased for residual fraction.

본 연구에서는 연안어장 준설퇴적물에 대한 영양염류(인공수 중 질산염과 인산염)의 흡착반응에서 흡착제, pH, 이온강도가 미치는 영향을 살펴보았다. 그리고 준설퇴적물을 이용해서 영양염류를 제거할 수 있는 가능성을 평가하고자했다. NO3--N(100μM, 10mM), PO43--P(100μM, 10mM)에 대한 흡착반응은 10분 이내에 완료되었고, 정상상태에서 100μM NO3--N과 100μM PO43--P가 각각 61%, 77% 제거 되었다. 900℃에서 준설퇴적물을 열처리했을 때 영양염류 제거율은 증가하지 않았다. CaO와 MgO 같은 첨가제를 사용하면 질산염의 제거율은 0%까지 감소했으나, 인산염 제거율은 98%까지 증가했다. 질산염과 인산염의 등온흡착은 Freundlich 식에 의해 잘 설명되었다(R2〉0.99). 흡착반응은 pH와 이온강도에 의해 거의 영향을 받지 않았다. 흡착반응시간이 짧고 영양염류 제거율이 상당히 높다는 연구결과는 연안어장 준설퇴적물이 영양염류 제거를 위해 실제로 사용될 수 있는 가능성을 보여준다.

This study is mainly focused on micellar effect of cetyltrimethyl ammonium bromide(CTABr) solution including alkylbenzimidazole(R-BI) on dephosphorylation of isopropyl-4-nitrophenylphosphinate(IPNPIN) in carbonate buffer(pH 10.7). The reactions of IPNPIN with R-BI⊖ are strongly catalyzed by the micelles of CTABr. Dephosphorylation of IPNPIN is accelerated by BI⊖ ion in 10-2 M carbonate buffer(pH 10.7) of 4×10-3 M CTABr solution up to 89 times as compared with the reaction in carbonate buffer by no benzimidazole(BI) solution of 4×10-3 M CTABr. The value of pseudo first order rate constant(kψ) of the reaction in CTABr solution reached a maximum rate constant increasing micelle concentration. Such rate maxima are typical of micellar catalyzed bimolecular reactions. The reaction mediated by R-BI⊖ in micellar solutions are obviously slower than those by BI⊖, and the reaction rate were decreased with increase of lengths of alkyl groups. It seems due to steric effect of alkyl groups of R-BI⊖ in Stern layer of micellar solution. The surfactant reagent, CTABr, strongly catalyzes the reaction of IPNPIN with R-BI and its anion(R-BI⊖) in carbonate buffer(pH 10.7). For example, 4×10-3 M CTABr in 1×10-4 M BI solution increase the rate constant(kψ=98.5×10-3 sec-1) of the dephosphorylation by a factor ca.25, when compared with reaction(kψ=3.9×10-4 sec-1) in 1×10-4 M BI solution(without CTABr). And no CTABr solution, in 1×10-4 M BI solution increase the rate constant(kψ=3.9×10-4 sec-1) of the dephosphorylation by a factor ca.39, when compared with reaction (kψ=1.0×10-5 sec-1) in water solution(without BI). This predicts that the reactivities of R-BI⊖ in the micellar pseudophase are much smaller than that of BI⊖. Due to the hydrophobicity and steric effect of alkyl group substituents, these groups would penetrate into the core of the micelle for stabilization by van der Waals interaction with long alkyl groups of CTABr.

The optimum annealing conditions of corn starch slurry were studied for RS4 type resistant starch production by phosphorylated cross-linking. When a corn starch slurry was cross-linked by using phosphate salts (STMP/STPP mixture) in the presence of 0.9%, 1.2% and 1.5% NaOH/st.ds, a high concentration of NaOH resulted in a rapid increase of the RS contents at the early reaction stage. However, similar RS contents were obtained after 12 h of cross-linking regardless of NaOH concentrations. The annealing treatment was conducted under various conditions such as pH between 2-10, temperature 40-60℃, time 0-14 h followed by phosphorylated cross-linking. The lower slurry pH was for the annealing treatment, the higher RS contents were obtained after cross-linking. When the slurry annealed for various period of time and temperature, a maximal amount of RS was formed after 2 h of annealing at 50℃ of annealing temperature of the starch slurry (pH 2.0). Therefore, an optimal annealing conditions at pH 2.0 and 50℃ for 2 h were proposed under the cross-linking conditions of sodium sulfate 10%/st.ds, NaOH1.2%/st.ds and 12 h of the reaction time. The RS contents were linearly increased with the increase of phosphate salt addition. The RS4 prepared under the optimal conditions contained RS 72.3% and its phosphorus content was 0.36%/st.ds, which was below the limit (0.4%/st.ds) of modified starch by Korea Food Additives Code.

The environmental changes related to hypoxic water mass were investigated at Gamak bay in summer times, June, July and August 2006. The hypoxic water mass was found, in first, at the northern area of Gamak bay on 27 June. This water mass has been sustained until the end of August and disappear on 13 September. In Gamak bay, the hypoxic water mass was closely related to geography. During the formation of oxygen deficiency, changes in dissolved nutrients was studied and found that on surface layer and lower layer, DIN were 0.80 μM~19.8 μM(6.03 μM) and 1.13 μM～60.83 μM(10.66 μM), and DIP were 0.01 μM～0.92 μM(0.24 μM), and 0.01 μM～3.57 μM(0.49 μM), respectively, far higher distribution on lower layer of the water where hypoxic water mass was occurred. The configuration of phosphorus was analyzed to figure out the possibility of release of phosphorus from sediments. It was found that the Labile-Phosphorus, which is capable of easy move to water layer by following environmental change was found more than 70%. Therefore, in Gamak bay, it was found that the possibility of large amount of release of soluble P into the water, while hypoxic water mass was occurred in deep layer was higher. It is suggested that DIP in the northern sea of Gamak bay mainly sourced from the soluble P from lower layer of the waters where hypoxic water mass was created more than that from basin. However, existence form of phosphorus in sediments during normal times, not during creation of hypoxic water mass, needs further study.

벼에서 인산흡수 관련 유전자를 이용하여 무기양분이 제한된 토양에서도 작물의 생장을 극대화시키는 무기영양 이용능력이 강화된 차세대 작물을 개발하고자 인산흡수력이 강화된 OsPT(Phosphate transporter)1, 4, 7, 8-OX 계통을 세대진전시켜 T5 세대에서 유전자의 안정적 도입을 확인하였다. 형질전환 계통들의 뿌리발달 상황을 조사해 본 결과, T/R율이 모든 형질전환 계통에서 동진벼보다 높은 경향을 보였다. OsPT1-OX 및 OsPT4-OX 계통은 모본인 동진벼에 비해 전반적으로 초장, 간장 및 수장은 짧았으나 OsPT7-OX 및 OsPT8-OX 계통은 주요 농업적 특성이 비슷하였다. 인산 무시용 시 OsPT1, 7, 8-OX 계통들은 출수기가 1~2일 정도 조숙화되었으나 인산흡수량이 과다하였던 OsPT4-OX계통은 오히려 2일 정도 만숙화되어 출수기 반응이 뚜렷하였다. 인산 무시용시 관행시비 대비 쌀수량 감소율은 동진벼가 18%로 컸으나 OsPT1-OX, 7, 8계통들은 각각 10, 15, 9%에 불과하였다. 인산 무시용시 모본인 동진벼에 비해 OsPT1, 4, 7, 8-OX 계통들은 출수기의 식물체 인산흡수량이 각각 104, 128, 26, 14% 증가하였으나 질소함량은 10, 16, 12, 5% 증가에 그쳤다. 동진벼에 비하여 P/N율이 높고 간장이 짧은 OsPT1-OX과 4-OX 계통은 (2N)P시험구에서 간장이 각각 6, 4 cm 회복되었다. OsPTs-OX의 인산함량(%)을 분석한 결과, OsPT4-OX >1-OX >7-OX >8-OX 순으로 나타난 반면, OsPT1-OX이 인산흡수율이 높으면서도 생육의 변화가 적어 개체당 총 인산흡수량(g/개체)은 OsPT1-OX >4-OX >7-OX >8-OX 순으로 OsPT1-OX이 인산흡수증진 신품종으로 가장 유망하였다. OsPT1-OX계통의 부위별 인산흡수량은 줄기와 잎에서 동진벼의 2.4배, 2.2배였으나 현미와 영에서는 차이가 없었다.

The roots of Platycodon grandiflorum has been widely used as a crude drug or a food stuff. Unfortunately, the output and the quality is not regular and highly dependent on the cultivation area and cultivation method. Therefore, seedling cultivation study of this plant under structure with various fertilizer supply was performed. As a result, significant big difference between ammonia nitrogen and nitrate nitrogen content was shown in the root at seedling stage while the difference was not significant in the aerial parts. Fresh weight of the root (7.73 g plant-1) was higher in the group treated with three major nutrients (N, P and K) than in those treated with three major nutrients and calcium or magnesium or both calcium and magnesium, and non-treated group (2.69 g plant-1). Total nitrogen content was recognized to be significantly correlated with root weight, plant height, number of leaves and weight of aerial parts. Ammonium nitrogen content was more correlated the growth of P. grandiflorum than nitrate nitrogen. For phosphoric acid, significant correlation was also shown with the four growth factors.

고씨동굴 내에 퇴적되어 있는 박쥐배설물을 대상으로 박쥐배설물 퇴적층에 생성된 인산염 및 황산염광물상들의 동정과 광물학적 특성연구를 통해 이들 광물상들의 지화학적 생성환경을 규명하고자 하였다. 박쥐배설물 내 및 하부에 침전된 물질들은 대부분 인산염 및 황산염광물로 확인되었다. 인산염광물로는 francoanellite, taranakite, ardealite, brushite, monetite가 관찰되었으며, 황산염광물로는 석고와 중정석이 관찰되었다. 인산염 광물은 하부로 갈수록 상대적으로 taranakite → francoanellite → ardealite → brushite → monetite의 변화양상을 보이는 반면 황산염광물 석고는 단면 전반에 걸쳐 확인되며, 특히 침전물 층 상부에 농집되어 나타난다. 중정석은 박쥐배설물 내에 소량 산재되어 나타난다. 인산염광물들의 침전과 이들의 수직적 광물상 변화양상은 박쥐배설물로부터 이들이 생성된 지화학적 조건이 산성환경이며, 하부로 갈수록 수분함량이 낮아지는 상대적인 건조한 환경이었음을 지시한다.

This study is mainly focused on micellar effect of cetylpyridinium chloride(CPyCl) solution including alkylbenzimidazole( R-BI) on dephosphorylation of diphenyl-4-nitrophenylphosphinate(DPNPIN) in carbonate buffer(pH 10.7). The reactions of DPNPIN with R-BI⊖ are strongly catalyzed by the micelles of CPyCl. Dephosphorylation of DPNPIN is accelerated by BI⊖ ion in 10 -2 M carbonate buffer(pH 10.7) of 4×10 -3 M CPyCl solution up to 100 times as compared with the reaction in carbonate buffer by no BI solution of 4×10 -3 M CPyCl. The value of pseudo first order rate constant(k m BI) of the reaction in CPyCl solution reached a maximum rate constant increasing micelle concentration. Such rate maxima are typical of micellar catalyzed bimolecular reactions. The reaction mediated by R-BI⊖ in micellar solutions are obviously slower than those by BI⊖, and the reaction rate were decreased with increase of lengths of alkyl groups. It seems due to steric effect of alkyl groups of R-BI⊖ in Stern layer of micellar solution. The surfactant reagent, cetylpyridinium chloride(CPyCl) , strongly catalyzes the reaction of diphenyl-4-nitrophenylphosphinate(DPNPIN) with alkylbenzimidazole (R-BI) and its anion(R-BI⊖) in carbonate buffer(pH 10.7). For example, 4×10 -3 M CPyCl in 1×10 -4 M BI solution increase the rate constant (kψ=1.0×10 -2 sec -1 ) of the dephosphorylation by a factor ca.14, when compared with reaction (kψ=7.3×10 -4 sec -1 ) in 1×10 -4 M BI solution(without CPyCl). And no CPyCl solution, in 1×10 -4 M BI solution increase the rate constant (kψ=7.3×10 -4 sec -1 ) of the dephosphorylation by a factor ca.36, when compared with reaction (kψ=2.0×10 -5 sec -1 ) in water solution(without BI). This predicts that the reactivities of R-BI⊖ in the micellar pseudophase are much smaller than that of BI⊖ . Due to the hydrophobicity and steric effect of alkyl group substituents, these groups would penetrate into the core of the micelle for stabilization by van der Waals interaction with long alkyl groups of CPyCl.

본 연구에서는 고비용의 실리카흄의 대체재로서 인산부산석고와 카올린을 활용한 시멘트매트릭스의 화학적, 기계적 성질에 대하여 분석하였다. 실험을 위하여 인산부산석고는 이수석고 형태인 건조석고, 반수석고, Ⅲ형 무수석고, Ⅱ형 무수석고로 실험용시료를 제조하였으며, 900℃에서 소성된 카올린은 서냉과 급냉의 형태로 제조된 메타카올린의 형태로 제조하였다. 또한 이재료를 활용하여 혼합시멘트를 제조하였으며, 제조된 시멘트를 사용하여 실리카 흄을 혼입한 시멘트 매트릭스와 재료적 성능을 비교 평가하였다. 실험결과 급냉제조된 메타카올린이 다른 재료에 비하여 성능이 우수한 것으로 분석되었다.

카올리나이트 KGa-1b (표준 점토)의 인산염 탈착 특성을 규명하기 위하여 벳치(batch) 흡착-탈착 실험을 실시하였으며, 탈착 과정은 연속추출법에 따라 pH 4에서 시행하였다. 인의 함량은 UV 분광분석기를 시용하여 측정하였으며, 이 때 파장은 820 nm를 이용하였다. 카올리나이트의 인산염 흡착-탈착 반응은 비가역적으로 일어나며, 흡착된 대부분의 인산염은 고착되는 경향을 나타낸다. 인산염 탈착 등온선은 반응 시간이 짧은 경우 프로인드리히 등온선에, 반응 시간이 긴 경우 탬킨 등온선에 더 일치하는 경향을 보인다. 인산염 탈착 반응은 초기의 빠른 반응과, 후기의 느린 반응으로 구분된다. 흡착된 인산염의 농도가 높아질수록 탈착률은 감소하는 경향을 보이며, 탈착 시간이 길어지면 탈착률은 감소하는 경향을 보여준다.

The effects of inorganic salts, inoculum concentration, aeration rate and shaking speed on insoluble phosphate solubilization by Pseudomonas fluorescens RAF15 were investigated. Soluble phosphate production was dependent on the presence of MgCl₂·6H₂O and MgSO₄·7H₂O in the medium. Supplementation of medium with 0.01% CaCl₂·2H₂O and 0.01% NaCl slightly increased soluble phosphate production. The optimal medium compositions for the solubilization of insoluble phosphate by P. fluorescens RAF15 were 1.5% glucose, 0.005% urea, 0.3% MgCl₂·6H₂O, 0.01% MgSO₄·7H₂O, 0.01% CaCl₂·2H₂O and 0.01% NaCl, respectively. Optimal inoculum concentration was 2.0%(v/v). Maximum soluble phosphate production was obtained with 20-50 ml/250-ml flask and 200 rpm of shaking speed, respectively. The addition of EDTA decreased cell growth and soluble phosphate production.