• 환경위생공학
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• 제9권2호
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• pp.1-7
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• 1994

Rainwater was collected in Seoul area from January 1991 to December 1993 (over 3years) and by the analysis of the chemical components contained in rainwater, investigated the components that effect on rainwater pH Through the above studies the following conclusions were obtained. 1) Method for Averaging pH Volume weighted method is considered to be acceptable providing that precipitation is measured at the same time when the samples are taken, without precipitation data a simple averaging method should be the next choice. 2) Annual average rainwater pH was 4.98 in 1991, 4.80 in 1992, 4.67 in 1993, measurement range was 3.6-8.1. 3) In the relationship between rainwater pH and rainfall amounts rainwater pH for light rain(<15mm rainfall) was existent in the wide range(pH 4-7), but for heavy rain was corresponded to the annual average values. 4) Annual frequency of pH was Birrndat the frequency($\gamma $) between the density of the [$H^{+}$] and pH in the rainwater(over 3years ), $NO_{3}^{-}$ was excellent and the obtained results was 0.62 in 1992. Also In the correlation coefficient($\gamma $) according to the pH range $SO_{4}^{2-}, NO_{3}^{-}$, were 0.85 ,0.68 at 3.6 $Cl^-$ was 0.99(1993). At 4.1$NO_{3}^{-}(\gamma=0.48)$ in 1992, SO_4^{2-}($\gamma$=0.54), $NO_{3}^{-}(\gamma$=0.72), $Cl^- (\gamma$=0.49) in 1993. 6) pH values gradually increased with increase in $Ca^{2+}/SO_{4}^{2-}$.

• 대한화학회지
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• 제32권3호
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• pp.260-266
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• 1988

${\beta},\;{\beta}$-Dichlorostyrene 유도체(p-H, p-Cl, $p-CH_3,\;및\;p-OCH_3$)에 대한 thioglycolic acid 및 cysteine의 친핵성 첨가반응속도를 자외선 분광분석법으로 측정하여 pH에 따르는 반응속도상수의 변화, 일반염기(general base) 및 치환기 효과등으로 부터 넓은 pH범위에서 실험치와 잘 일치하는 반응속도식을 구하였고, 실험사실에 잘 맞는 반응 메카니즘을 제안하였다. 즉 pH 9.0 이상에서의 반응속도는 sulfide anion이 pH $9.0{\sim}7.0$에서는 thioglycolic acid 및 cysteine의 중성분자와 그의 anion들이 경쟁적으로 첨가되며 pH 7.0 이하에서는 thioglycolic acid 및 cysteine의 중성분자만이 첨가됨을 알았다.

• 미생물학회지
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• 제13권2호
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• pp.59-63
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• 1975

When the enzyme preparations were at various temperatures for 1 hour, the thermal stability for the enzyme was maximum at $30{\circ}C.$ The optimum temperature for the enzyme activity was at $40{\circ}C.$ When the enzyme preparations were exposed to various pHs for 22 hours, the enzyme stability was maximum at pH 3.8, and it was decreased gradually as the pH rose up to 4.8, above which the stability was greatly restored. When the exposure period was extended from 22 to pH's 3.0 and 5.9, but the stability tended to rise at pH's below 3.0 and above 5.9. The optimum pH for the enzyme activity was obtained at 4.8.

• 대한화학회지
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• 제35권3호
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• pp.268-274
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• 1991

${\beta}$-nitrostyrene 유도체(p-H, p-Cl, p-CH$_3$, p-OCH$_3$, p-NO$_2$)에 대한 thiourea의 친핵성 첨가반응속도를 자외선 분광분석법으로 측정하여 pH에 따르는 반응속도 상수의 변화, general base 및 치환기 효과등으로부터 넓은 pH 범위에서 실험치와 잘 일치하는 반응속도식을 구하였고, 실험사실에 잘 맞는 반응 메카니즘을 제안하였다. 즉, pH 9.00 이상에서의 반응속도는 hydroxide ion의 농도에 비례하는 sulfide anion이 첨가되는 전형적인 Michael type의 반응이 일어나며, pH 9.00 ~ 7.00에서는 thiourea의 중성분자와 그의 anion들이 경쟁적으로 첨가되며 pH 7.00 이하에서는 thiourea의 중성분자만이 첨가됨을 알았다.

• Bulletin of the Korean Chemical Society
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• 제20권6호
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• pp.712-714
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• 1999

The rate constants for the nucleophilic addition of potassium cyanide to α,N-diphenylnitrone and its derivatives (p-OCH3, p-CH3, p-Cl, and p-NO2) were determined by ultraviolet spectrophotometer at 25℃, and the rate equations which can be applied over a wide pH range were obtained. On the basis of pH-rate profile, adduct analysis, general base catalysis and substituent effect, a plausible mechanism of this addition reaction was proposed: At high pH, the cyanide ion to carbon-nitrogen double bond was rate controlling, however, in acidic media, the reaction proceeded by the addition of hydrogen cyanide molecule to carbon-nitrogen double bond after protonation at oxygen of a,N-diphenylnitrone. In the range of neutral pH, these two reactions occured competitively.

• Nuclear Engineering and Technology
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• 제18권3호
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• pp.194-199
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• 1986

수용액중에 극미량의 Am의 거동이 pH변화에 따라 변화하는 것을 원심분리법으로 조사하였다. 이 연구에서 평형시간을 2~3주 연장, 방사성 코로이드 형성에 있어서의 시간효과를 조사하였다. 또한 실리카겔 및 Fe$^{3+}$ 등 외부 물질을 첨가하여 그 효과를 조사하였으며, 또한 진한 전해질물질의 효과도 아울러 조사하였다. 그 결과, pH 6에서 Am은 불순입자, 또는 용기벽과 이온 흡착과정으로 급속히 흡착이 일어났다. 외부물질의 첨가는 Am의 흡착을 촉진하였으며, 진한 전해질물질의 첨가로 흡착이 방해되었다. pH 7에서 Am은 pH 6조건과는 전혀 다른 거동을 나타내었다. 일부 Am은 용기 기벽에서 빠른 흡착이 일어났으며, 1~2일 후에 일부는 탈착되었다.

• Tribology and Lubricants
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• 제20권2호
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• pp.97-101
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• 2004

This paper reports the studies on the wear-corrosion behavior of Al-Mg alloy in various pH environments. In various pH of sea water, corrosion and wear-corrosion loss of Al-Mg alloy were investigated. Also, the polarization test of Al-Mg alloy using potentiostat/galvanostat was carried out. And the rubbed surface of Al-Mg alloy using scanning electron micrographs after wear-corrosion test was examined in various pH values of sea water. The main results are as following : The polarization resistance of Al-Mg alloy in pH 4 solution is higer than that in pH 6.7 solution, and the corrosion current density in pH 4 is controlled than in pH 6.7 solution. The wear-corrosion loss of Al-Mg alloy with lowering pH becomes sensitive. As the oxide product of Al-Mg alloy appears granular structure and exholiation phenomenon, wear-corrosion loss of Al-Mg alloy increases.

• 대한화학회지
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• 제26권6호
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• pp.407-413
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• 1982

3,4-methylenedioxyphenylmethylene malononitrile에 대한 cysteine의 친핵성 첨가반응 속도를 측정하여 염기성 및 산성용액에서의 반응메카니즘을 제안하였고 넓은 pH범위에서 잘 맞는 반응속도식을 구했다. 이 반응속도식으로 부터, pH 9.0 이상에서는 hydroxide ion 농도에만 비례하고, pH 6.0 이하에서는 cysteine의 중성분자만이 첨가하며, pH 7~9.0에서는 cysteine 중성분자와 그의 음이온이 경쟁적으로 첨가됨을 알 수 있었고 첨가되는 cysteine 중성분자와 음이온의 비도 계산할 수 있었다.

• 대한화학회지
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• 제44권5호
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• pp.429-434
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• 2000

Styryldiphenylphosphine(SDPO)의 가수분해 속도상수를 자외선 분광법으로 측정하여 넓은 pH에서 잘 맞는 반응속도식을 구하였다. pH에 따르는 속도상수의 변화, 가수분해 생성물의 확인, 일반염기 및 치환기 효과 등으로부터 실험 결과에 잘 맞는 반응 메커니즘을 제안하였다. 즉 pH 4.5 이하에서는 phosphine oxide기의 산소에 양성자가 첨가된 다음 탄소 이중결합에 물의 첨가가 일어나 가수분해가 진행되며, pH 4.5-8.0 사이에서는 물분자와 수산와 음이온의 첨가가 경쟁적으로 일어나 반응이 진행되었고, pH 8.0 이상에서는 반응속도 상수가 수산화 음이온의 농도에만 비례함을 알았다.

• 약학회지
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• 제29권4호
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• pp.220-222
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• 1985

Rifampicin reacts with cupric ion to produce rifampicin-Cu(II) chelate (2:1) at pH 6.5, which can be extracted with methylisobutylketone (MIBK). Therefore, rifampicin can be quantitatively, determined by measuring the quantity of Cu(II) in the organic phase by atomic absorption spectrophotometry. Because higher absorbance ratio was obtained in pH 6.0~7.0, buffer solution at pH 6.5 was used in this measurement. Linear relationship was found between absorbance and concentration in the range of 1.0~4.0${\times}10^{-4}M$. This method might be applicable to the determination of rifampicin in the preparations.