• 한국잠사곤충학회지
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• 제27권1호
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• pp.12-17
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• 1985

1982년 충남 부여와 충북 옥천, 1983 경북 상주에서 생산된 묘목의 활착율이 불량한 사례가 발생하여 그 원인을 구명하기 위해 묘포지 토양의 이화학성을 조사하는 한편, 1984년 충북의 상묘생산업자 21개, 115개 포장의 토양분석을 행한 결과 다음과 같았다. 1. 죽은 상묘를 증상별로 구분한 결과 붕소부족 증상이 59%였으며, 아무런 외형적인 증상이 없이 발아가 안 되는 경우가 34.9%, 그리고 연폐 증상을 보인 묘목은 6.1%였다. 2. 상묘의 활착율이 나빴던 포장은 하천부지의 논토양으로 유효토심이 20cm 내외이었으며 그 밑에는 거친 모래 또는 자갈층이 있었다. 3. 토양의 화학성은 강산성이었으며, Ca, Mg의 함량이 낮았으며, 특히 B의 함량이 매우 낮았다. 유효인산과 칼리는 높은 경우도 있었다. 4. 논토양에 묘포는 설치한 경우에는 객토를 하였거나, 붕사를 준 경우에 활착율이 높은 것으로 나타났다. 5. 충북의 상묘포지 토양은 전면적 60.8ha 중 52.8%를 논토양이 점유하였고, pH6.5인 필지가 90.5%, 칼리 0.5me/100g 이하가 87.0% Ca은 6.5me/100g 이하가 40.8%, Mg은 2.00me/100g 이하가 94.8%, B은 0,3ppm 이하가 99.1%나 되었다.

• Bulletin of the Korean Chemical Society
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• 제30권2호
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• pp.383-388
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• 2009

Rates of solvolyses of diphenyl thiophosphorochloridate ($(PhO)_2$PSCl, 1) in ethanol, methanol, and aqueous binary mixtures incorporating ethanol, methanol, acetone and 2,2,2-trifluoroethanol (TFE) are reported. For four representative solvents, studies were made at several temperatures and activation parameters were determined. The 30 solvents gave a reasonably precise extended Grunwald-Winstein plot, correlation coefficient (R) of 0.989. The sensitivity values (l = 1.29 and m = 0.64) of diphenyl thiophosphorochloridate ($(PhO)_2$PSCl, 1) were similar to those obtained for diphenyl phosphorochloridate ($(PhO)_2$POCl, 2), diphenylphosphinyl chloride ($Ph_2$POCl, 3) and diphenylthiophosphinyl chloride ($Ph_2$PSCl, 4). As with the previously studied of 3~4 solvolyses, an $S_N$ pathway is proposed for the solvolyses of diphenyl thiophosphorochloridate (1). The activation parameters, ${\Delta}H^{\neq}\;(=11.6{\sim}13.9\;kcal{\cdot}mol^{-1})\;and\;{\Delta}S^{\neq}\; (=\;-32.1\;{\sim}\;-42.7\;cal{\cdot}mol^{-1}{\cdot}K^{-1})$, were determined, and they were in line with values expected for an $S_N$2 reaction. The large kinetic solvent isotope effects (KSIE, 2.44 in MeOH/MeOD and 3.46 in $H_2O/D_2$O) are also well explained by the proposed $S_N$2 mechanism.

• Applied Biological Chemistry
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• 제20권3호
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• pp.300-309
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• 1977

The information related to the heavy metal pollution in the environment was obtained from studies on the effects of pH, phosphate and soil properties on the adsorption of metal ions (Cd, Cu, Ni, and Zn) by soils. Three soil materials; soil 1 with low CEC (8.2 me/100g) and low organic carbon content (0.34%); soil 2 with high CEC (36.4 me/100g) and low organic carbon content (1.8%) and soil 3 with high CEC (49.9 me/100g) and high organic carbon content (14.7%) were used. Soils were adjusted to several pH's and equilibrated with metal ion mixtures of 4 different concentrations, each having equal equivalents of each metal ion (0.63, 1.88, 3.12 and 4.38 micromoles per one gram soil with and without 10 micromoles of phosphate per one gram soil). Reported here are the results of the equilibrium study on soil I. The rest of the results on soil 2 and soil 3 will be repoted subsequeutly. Generally higher metal ion concentration solution resulted in higher final metal ion concentrations in the equilibrated solution and phosphate had minimal effect except it tended to enhance removal of cadmium and zinc from equilibrated solutions while it tended to decrease the removal of copper and nickel. In soil 1, percentages of added metal ions removed at pH 5.10 were; Cu 97, Ni 69, Cd 63, and Zn 55, while increasing pH to 6.40, they were increased to Cu 90.9, Zn 99, Ni 96, and Cd 92 per As initial metal ion concentration increased, final metal ion concentrations in the equilibrated solution showed a relationship with pH of the system as they fit to the equation $p[M^{++}]=a$ pH+b where $p[M^{++}]=-log$[metal ion concentration in Mol/liter]. The magnitude of pH and soil effects were reflected in slope (a) of the equation, and were different among metal ions and soils. Slopes (a) for metal ions in the aqueous system are all 2. In soil 1 they were; Zn 1.23, Cu 0.99, Ni 0.69 and Cd 0.59 at highest concentration. The adsorption of Cd, Ni, and Zn in soil 1 could be represented by the Iangmuir isotherm. However, construction of the Iangmuir isotherm required the correction for pH differences.

• Natural Product Sciences
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• 제18권1호
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• pp.47-51
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• 2012

Among 38 Vietnamese medicinal plant extracts investigated for their ${\alpha}$-glucosidase inhibitory activity, 35 extracts showed $IC_{50}$ values below $250{\mu}g/mL$. The MeOH extracts of the heartwood of Oroxylum indicum, the seeds of Caesalpinia sappan, and the fruits of Xanthium strumarium exhibited strong ${\alpha}$-glucosidase inhibitory activity with $IC_{50}$ values less than $50{\mu}g/mL$. Fractionation of the MeOH extract of the heartwood of O. indicum led to the isolation of oroxylin A (1), oroxyloside (2), hispidulin (3), apigenin (4), ficusal (5), balanophonin (6), 2- (1-hydroxymethylethyl)-4H,9H-naphtho[2,3-b]furan-4,9-dione (7), salicylic acid (8), p-hydroxybenzoic acid (9), protocatechuic acid (10), isovanillin (11), and ${\beta}$-hydroxypropiovanillon (12). Compounds 1 - 3, 5, 6, 8, 10, and 12 showed more potent activities, with $IC_{50}$ values ranging from 2.13 to $133.51{\mu}M$, than a positive control acabose ($IC_{50}$, $241.85{\mu}M$). The kinetic study indicated that oroxyloside (2) displayed mixed-type inhibition with inhibition constant (Ki) was $3.56{\mu}M$.

• Journal of the Korean Wood Science and Technology
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• 제43권5호
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• pp.591-599
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• 2015

Cercidiphyllum japonicum leaves were collected, air-dried and extracted with 70% aqueous acetone, then concentrated and sequentially fractionated using n-hexane, methylene chloride ($CH_2Cl_2$), ethylacetate (EtOAc), and $H_2O$. A portion of EtOAc fraction (10 g) was chromatographed on a Sephadex LH-20 column, by the successively elution with various aqueous $MeOH-H_2O$ (1:9, fraction $1-2{\rightarrow}3:7$, fraction $3-5{\rightarrow}1:1$, fraction $6-9{\rightarrow}7:3$, fraction $10-13{\rightarrow}9:1$, fraction 14-16). Compound 2 was isolated from fraction 6 and compound 1 was separated from fraction 11 and 12. Compound 3 and 4 were purified from fraction 13. The isolated compounds were elucidated as quercetin-3-O-${\alpha}$-L-rhamnopyranoside (1), chlorogenic acid (2), quercetin-3-O-${\alpha}$-L-arabinofuranoside (3) and quercetin-3-O-${\beta}$-D-xylopyranoside (4) by the spectral and literature data, and by comparison with the authentic samples. These compounds were reported, for the first time, from the extracts of C. japonicum leaves. Also chlorogenic acid (2) has never been reported before in domestic tree species and can be used as an index compound for C. japonicum.

• 한국축산식품학회지
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• 제29권6호
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• pp.719-725
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• 2009

헤테로고리 아민은 높은 돌연변이성과 발암 가능성을 가진 물질로, 단백질이 높게 함유된 식품의 가열 중 발생한다. 본 실험에서는 $220^{\circ}C$에서 양면을 10분씩 가열 조리한 쇠고기 패티를 microwave를 이용하여 예열처리를 하였을 때 나타나는 HCAs의 생성량에 대한 영향을 분석하였다. 헤테로고리 화합물의 분석을 위해 전처리 과정에서 solidphase extraction 방법을 이용하였고, LC/MS로 정량과 정성분석을 하였다. 시료에서는 9개의 HCAs(Trp-P-2, Trp-P-1, Glu-P-1, Glu-P-2, Norharman, Harman, $A{\alpha}C$, MeIQx, PhIP)가 검출되었으며 이 중 Norharman, Harman, PhIP가 상대적으로 높은 함량이었다. 1분 동안의 microwave 예열 처리는 검출된 대부분의 HCAs 생성을 무처리 대조군에 비해 90% 이상 감소시켰다. Amino-carbolines류의 HCAs 경우, 1분의 microwave preheating 처리가 가장 효과적이었고 PhIP가 대부분의 함량을 차지하는 amino-imidazoazaarens류는 microwave preheating 시간이 증가할수록 뛰어난 HCAs 감소효과를 나타내었다.

• 대한화장품학회지
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• 제19권1호
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• pp.20-30
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• 1993

본 연구는 역상 HPLC를 이용하여 Pb(IEAA-NR)2 (R=H, CH3, C3H7, C6H5, C4H9) 킬레이트를 동시 분리하기 위한 최적 분리 조건을 조사하고 이들의 용리거동에 관련된 인자들과의 관계를 검토하였는데 그 결과는 다음과 같다. 1. 각 Pb(IEAA-NR)2 킬레이트의 분리에 대한 기기의 최적 조건을 실험적으로 측정한 결과는 다음과 같다. 분리관 : Micropak MCH-5 (4.0 mm I.D. $\times$ 15 cm L, Particle size 5 $\mu\textrm{m}$) 용리액 : MeOH / H20 (73/27) 흐름속도 : 0.7 ${\mu}\ell$/min. 시료주입량 : 4 ${\mu}\ell$ 검출기 : UV 검출기 (254 nm) 2. 용리액의 흐름속도는 0.7${\mu}\ell$/min. 일때 적당한 분리 시간과 좋은 분리도를 나타내었다. 3. 시료 용매가 킬레이트의 머무름 시간에는 큰 영향을 주지 않았으며 금속 킬레이트간의 겸침 현상이 줄어들고 봉우리 면적이 큰 CH3CN을 사용하였다. 4. 용리액의 조성은 MeOH/H2O 의 비가 73/27 으로써 대개의 경우에 lig k' 값이 0$\leq$log k' $\leq$1을 잘 만족하지 않았으며 전체적으로 적당한 분리시간과 좋은 분리도를 나타내었다. 5. Pb(IEAA-NR)2 킬레이트의 log k' 값을 이성분 용매계에서 물의 부피 분율에 대하여 plot한 결과 이들이 직선적인 관계를 가지는 것으로 보아 Pb(IEAA-NR)2 의 머무름은 소수성 효과(Hydrophobic effect)에 크게 기인 한다는 것을 알 수 있었다.

• 한국토양비료학회지
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• 제6권4호
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• pp.205-211
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• 1973

화강암(花崗岩), 화강섬녹암(花崗閃綠岩), 섬녹암(閃綠岩), Arkose 질사암(質砂岩) 및 Tertiary 혈암(頁岩)등에 유래(由來)된 사과원(園) 11개처(個處)에서 층위별(層位別)로 토양(土壤)을 채취(採取)하여 그 리화학적성질(理化學的性質)을 조사한 결과(結果)는 다음과 같다. 1. 일반적(一般的)으로 토성(土性)은 사질(砂質)이고 pH($H_2O$)는 4.35~6.75로서 약산성(弱酸性) 내지(乃至) 중성(中性)이고, 표토(表土)의 부식함량(腐植含量)은 1.14~5.58%, 질소(窒素)는 0.065~0.209%이나 하층(下層)으로 내려갈수록 감소(減少)하고 있다. 2. 표토(表土)의 치환성염기함량(置換性鹽基含量)은 4.89~17.81me/100g로서 비교적(比較的) 적고(Ca>Mg>K>Na). 염기치환용량(鹽基置換容量)은 7.74~21.72me/100g 범위(範圍)이며 염기포화도(鹽基飽和度)는 22.52~94.62% 범위이다. 3. 표토(表土)의 인산(燐酸)은 35.5mg/100g 이하(以下)로서 매우 적고, 가리(加里)(79.2~7.2mg/100g), 유효태동 (有效態銅 )(1.0~16.9ppm), 수용성붕소(水溶性硼素)(0.18~0.72ppm) 등은 표토(表土)에 많고 하층(下層)으로 내려갈수록 감소(減少)되었으며 망간은 pH 에 따라 그 함량(含量)의 차이(差異)를 볼 수 있었든바 pH 4~6에서는 수용성(水溶性)망간이 0.42~17.8ppm. 치환성(置換性)망간이 9.82~66.83ppm이나 PH 6이상(以上) 되는 곳에서는 수용성(水溶性)망간이 0.70ppm 이하(以下), 그리고 치환성(置換性)망간이 22.25ppm 이하(以下)로서 현저히 적었다.

• 한국세라믹학회지
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• 제39권9호
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• pp.813-817
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• 2002

Magnetoelectric(ME) laminate composites of $Pb(Mg_{1/3}Nb_{2/3})O_3-PbTiO_3 (PMN-PT)$ and Terfenol-D were prepared by sandwiching single crystals of PMN-PT between Terfenol-D disks. The magnetoelectric voltage coefficient (dE/dH) of the composite was determined to be 10.30 V/cm${\cdot}$Oe, at 1 kHz and under a dc magnetic bias of 0.4 T. The value of dE/dH is ∼80 times higher than either that of naturally occurring magnetoelectrics or artificially-grown magnetoelectric composites. This superior magnetoelectric voltage coefficient is attributed to the high piezoelectric voltage constant as well as the high elastic compliance of PMN-PT single crystal and the large magnetostrictive response of Terfenol-D.

• BMB Reports
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• 제29권1호
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• pp.73-80
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• 1996

The effect of albumin on phosphatidylcholine (PC) metabolism in Hep-G2, 3T3-H.ras, and 3T3 cells pre-labelled with [Me-$^3H$]choline was studied. The [$^3H$]choline was more efficiently taken up and incorporated into cellular phospholipids in 3T3-H.ras cells than in Hep-G2 and 3T3 cells. In each of the three cell lines, most of the [$^3H$]choline metabolized into the phospholipids was incorporated into PC and only minor was incorporated into lysophosphatidylcholine (LPC). Bovine serum albumin stimulated the release of [$^3H$]LPC and [$^3H$]PC from each of the three cell lines pre-labelled with [$^3H$]choline. [$^3H$]PC was also released in the absence of albumin but [$^3H$]LPC was not. The efficiency of LPC secretion represented as the proportion of medium [$^3H$]LPC to cellular [$^3H$]choline lipid during a chase period is approximately 9 to 14 times greater in 3T3 cells compared with the transformed 3T3-H.ras and Hep-G2 cells. A similar comparison of published data for rat hepatocytes with Hep-G2 shows secretion to be 35~75 times greater from the rat hepatocytes than from Hep-G2. Also, PC secretion from 3T3 cells was 1.6 times more effective than from 3T3-H.ras, whereas rat hepatocytes secrete PC 2.8~3.8 times more effectively than does Hep-G2. The measurement of specific radioactivity of cellular PC in pre-labelled 3T3 cells showed it to be similar to that of the secreted PC. However, the specific radioactivity of secreted LPC was markedly lower than that of the cellular PC, which suggests that LPC is being secreted from a PC pool distinct from that used for PC secretion.