• 제목/요약/키워드: $Na_2S_2O_3$

검색결과 859건 처리시간 0.026초

염산(鹽酸)Promazine 주사제(注射劑)의 안정화(安定化)에 관한 연구(硏究) (Study on Stabilization of Promazine Hydrochloride Injection)

  • 이완하;지웅길;양재헌
    • Journal of Pharmaceutical Investigation
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    • 제3권3호
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    • pp.5-15
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    • 1973
  • The stabilizing effect of promazine hydrochloride injectin was tested by irradiation of sun lamp(5,000 Lux) on their acid solution sealed in ampules under various stabilizers. The result of experimentation on the color change, the remaining proportion and the half life of promazine hydrochloride solution is as follows. 1. Instability of promazine hydrochloride solution is mainly caused by the sunlight and oxygen. 2. The pH range of promazine hydrochloride injection is recommended to $pH\;4.4{\sim}5.2$ 3. The decomposition of promazine hydrochloride by the sunlight is composed of pseudo zero order reaction when It maintains colorless solution. 4. The half life of 0.5% promazine hydrochloride injection was 30 hrs. under sun lamp irradiation, but it was delayed to 84 hrs. by the simple stabilizer and to 175 hrs. by compound stabilizer. 5. The stabilizing effect of promazine .hydrochloride injection adding sod. metabisulfite$(Na_2S_2O_5)$ was most excellent in various simple stabilizers and adding $Na_2S_2O_5$ to nicotinic acid, $Na_2S_2O_5$ to nicotinamide were more excellent than other compound stabilizers.

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유기수은의 신경독성에 대한 셀레늄의 보상작용 (Interaction of Sodium Selenite on Neurotoxicity Induced by Methylmercuric Chloride)

  • 박정수;이효민;정용;신동천;노재훈;문영한
    • Journal of Preventive Medicine and Public Health
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    • 제25권1호
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    • pp.13-25
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    • 1992
  • This study was conducted to investigate the mechanism of protective effect by sodium selenite in methylmercuric chloride neurotoxicity, increasing intracellular $Ca^{2+}$concentration of the neuron. Methylmercuric chloride of 3mg/kg of body weight was administered simultaneously with sodium selenite of 5mg/kg and pretreatment of sodium selenite via intraperitoneal injection to rats. Also, effect of methylmercuric chloride($25{\mu}M,\;50{\mu}M,\;100{\mu}M$) and sodium selenite($200{\mu}M$) on free intrasynaptosomal $Ca^{2+}$ concentration were studied using the fluorescent $Ca^{2+}$ indicator fura -2 in vitro. After the treatment, at 6, 24, and 48 hours later, mercury in the cerebral cortex, liver and kidney tissues, succlnic dehydrogenase activities, adenosin-5'-triphosphate concentration, acetylcholinesterase activities, and intracellular $Ca^{2+}$ concentration in the cerebral cortex were determined in vivo. Cerebral synaptosomes of rats were incubated with methylmercuric chloride and sodium selenite in Hepes buffer for 10 minutes and free intrasynaptosomal $Ca^{2+}$ concentration were measured with fura-2 in vitro. The results were summarized as follows ; 1. The combined administration of $CH_3HgCl$ and $Na_2SeO_3$ and pretreatment of $Na_2SeO_3$ according to time significantly more increased in the cerebral cortex and decreased in the liver, kidney mercury concentrations compared to the administration of $CH_3HgCl$ only. 2. The combined administration of $CH_3HgCl$ and $Na_2SeO_3$ and pretreatment of $Na_2SeO_3$ increased more succinic dehydrogenase and acetylcholinesterase activities compared to the administration of $CH_3HgCl$ only. Particularly pretreatment of $Na_2SeO_3$ significantly more compared to the administration of $CH_3HgCl$ only. The concentration of adenosine-5'-triphosphate in $Na_2SeO_3$ treatment groups revealed a favourable effect compared to the administration of $CH_3HgCl$ only. 3. Intracellular $Ca^{2+}$ concentration in administration of $CH_3HgCl$ only was increased significantly more than control group in all test hours but was increased significantly more at 48 hours only after treatment in combined administration of $CH_3HgCl$ and $Na_2SeO_3$ and pretreatment of $Na_2SeO_3$ according to time interval more decreased significantly intracellular $Ca^{2+}$ concentration compared to the administration of $CH_3HgCl$ only. 4. Free intrasynaptosomal $Ca^{2+}$ concentration in the combined administration of $CH_3HgCl$ and $Na_2SeO_3$ was decreased ($24%{\sim}40%$) significantly more than the administration of $CH_3HgCl$ only. From the above results, the specific dosage of $Na_2SeO_3$ decreased increment of intracellular $Ca^{2+}$ concentration induced by administration of $CH_3HgCl$. These findings suggest the protective mechanism of $Na_2SeO_3$ on the neurotoxicity of $CH_3HgCl$.

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Cu/TaN CMP시 $H_2O_2$ 적정방법 (Titration methods of $H_2O_2$ in Cu/TaN CMP)

  • 유해영;김남훈;김상용;김태형;장의구
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2004년도 춘계학술대회 논문집 반도체 재료 센서 박막재료 전자세라믹스
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    • pp.38-41
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    • 2004
  • The oxidizer plays an important role in the metal chemical mechanical polishing(CMP) slurry. Currently, the oxidizer used in CMP slurry is nearly divided into several kinds such as $Fe(NO_3)_3$, $H_2O_2$, $KIO_3$, and $H_5IO_6$. It is generally known that oxidizer character of $H_2O_2$ is more effective than other oxidizers. In this work, we have been studied the characteristics for the $H_2O_2$ concentration of copper slurry, which can applicable in the recent semiconductor manufacturing process. Also, it plays an important role in the planarization of copper films using copper slurries during micro-electronic device fabrication. In this work, we confirmed that removal rate of Cu/TaN changed by $H_2O_2$ concentration on copper slurry. And we used $KMnO_4$ in the measurement method of $H_2O_2$. In analysis results, we confirmed that the difference of results is large. We thought that the difference was due to organic component existence. So in titration method of $H_2O_2$ concentration, we used $Na_2S_2O_3$ instead of $KMnO_4$ as solution. Consequently, using the titration method, we could calculate correct data reduced error. And $H_2O_2$ concentration has been adjusted to the target concentration of 0.1 wt%.

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Redox Behavior of Sn and S in Alkaline Earth Borosilicate Glass Melts with 1 mol% Na2O

  • Kim, Ki-Dong;Kim, Hyo-Kwang
    • 한국세라믹학회지
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    • 제46권3호
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    • pp.271-274
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    • 2009
  • Redox investigation of Sn and S ion was attempted in alkaline earth borosilicate glass melts with only 1 mol% $Na_2O$ by means of Square Wave Voltammetry (SWV). According to voltammograms, there was only one peak due to $Sn^{4+}/Sn^{2+}$ in melt doped with $SnO_2$. The calculated standard enthalpy and entropy of the reduction of $Sn^{4+}$ to $Sn^{2+}$ were 116kJ/mole and 62 J/mol K, respectively. The determined redox ratio, [$Sn^{2+}$] / [$Sn^{4+}$] in the temperature range of $1300{\sim}1600^{\circ}C$ was in $0.4{\sim}2.1$. On the contrary, in the voltammogram of melt doped with $BaSO_4$ there was no peak due to $S^{4+}/S^o$ but shoulder that might be attributed to the adsorption of sulfur at the electrode. The absence of the peak related with $S^{4+}/S^o$ was discussed from the view-point of the thermal decomposition behavior of $BaSO_4$ in the glass batch.

경남지역 양액재배용 지하수의 이온 분포특성 (Ionic Characteristics of the Ground Water for Hydroponics in Kyeongnam Area)

  • 이영한;전성건;황연현;조강희;신원교
    • 생물환경조절학회지
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    • 제7권3호
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    • pp.246-252
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    • 1998
  • 1995년 경남지역에서 양액재배 원수로 사용되고 있는 77개 농가의 지하수 중의 무기성분 농도를 분석한 결과는 다음과 같다. 지하수의 깊이는 10~500m, pH는 6.2~8.4, EC는 0.11~1.44dS/m이었다. 1 liter당 무기성분의 평균함량은 N $H_{4}$-N 0.3mg, N $O_{3}$-N 3.1mg, P $O_{4}$$^{3-}$ 0.5mg, $Ca^{2+}$ 25.4mg, $Mg^{2+}$ 11.5mg, $Na^{+}$ 21.7mg, C $l^{-}$ 42.6mg, S $O_{4}$$^{2-}$ 72.5mg였다. 지하수의 pH와 $Mg^{2+}$(0.34$^{**}$ ), $Ca^{2+}$(0.33$^{**}$ ) 및 EC(0.29$^{**}$ ) 사이에 유의적인 정(+)의 상관을 보였다. 또한 EC와 $Na^{+}$(0.68$^{**}$ ), $Ca^{2+}$(0.67$^{**}$ ), S $O_{4}$$^{2-}$(0.62$^{**}$ ), $Mg^{2+}$(0.60$^{**}$ ), N $H_{4}$-N(0.36$^{**}$ ), C $l^{-}$(0.53$^{**}$ ) 및 $K^{+}$(0.26$^{**}$ ) 간에도 유의적인 정(+)의 상관을 보였다..

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적외선 분광법을 이용한 Perfluorostearic Acid의 이온화 연구 (Infrared Spectroscopic Studies on the Ionization of Perfluorostearic Acid)

  • 김욱수;하기룡
    • 공업화학
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    • 제19권1호
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    • pp.111-116
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    • 2008
  • 적외선 분광법을 이용하여 하부상의 다양한 pH(3~11) 변화 및 금속이온($Na^+$, $Ca^{2+}$, $La^{3+}$) 존재에 따른 perfluorostearic acid(PFS)의 이온화 거동에 관한 연구를 수행하였다. Langmuir-Blodgett (LB) 수조의 하부상에 존재하는 pH 변화 및 금속이온의 종류에 따른 PFS의 -COOH의 C = O 신축진동 피크와 $COO^-$ 피크의 이동 및 강도의 변화를 관찰한 결과 하부상 수용액의 pH가 같은 경우에는 PFS의 -COOH 그룹의 C = O 피크 세기의 감소가 $La^{3+}$ > $Ca^{2+}$ > $Na^+$의 순으로 나타났다. 이는 PFS에 대한 친화도가 $La^{3+}$가 가장 크며, $Ca^{2+}$$Na^+$의 순서로 감소한다는 것을 알 수 있다. 또한 증류수 하부상에서 생성된 perfluorostearate 이온의 몰분율을 측정한 IR 스펙트럼으로부터 계산한 결과 약 pH 3의 낮은 pH 값에서도 50% 이상의 perfluorostearate 이온이 생성되는 것을 관찰하였으며, 이러한 결과는 PFS의 이온화도가 stearic acid (SA)보다 높은 것을 나타낸다.

(60-x)SiO2-40Na2O-xCaO(x=0∼15wt%)조성유리계의 조성, 온도 및 전기전도도간의 상관특성 (Relations between Composition, Temperature and Electrical Conductivity of (60-xSiO2-40Na2O-xCaO(x=0∼15wt%) Glass System)

  • 정영준;김영석;이규호;김태호;진현주;류봉기
    • 한국재료학회지
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    • 제17권8호
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    • pp.414-419
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    • 2007
  • We report the electrical conductivity of the mixed alkali silicate glasses in the system (60-x)$SiO_2-40Na_2O-xCaO(x=0\sim15wt%)$ in the temperature range from $150^{\circ}C$ to $620^{\circ}C$. In the range from $150^{\circ}C$ to glass transition temperature$(T_g)$, the electrical conductivities of glass samples had a tendency to be proportion with temperature. The glasses of containing over 7.5wt% CaO showed lower conductivities than the glasses of containing 0 and 5wt% CaO because two kinds of alkali ions$(Na^+,\;Ca^{2+})$ were obstructed each other. On the other hand, in the range from $T_g$ to $620^{\circ}C$, the electrical conductivity of glasses($7.5{\leq}x{\leq}12.5$) was unstable and decreased in some region. From XRD results, the $Na_4Ca(SiO_3)_3$ phase were observed in these glasses. This means the alkali ions didn't behave as carrier, it seems that this caused the conductivities decrease. In case of glass of containing 15wt% CaO, any crystal phase were not observed. This means the alkali ions behaved as carrier, it consequently seems the conductivity increased.

강원도지역 탄산수의 환경동위원소적 특성 (Environmental Isotope Characteristics of $CO_2$-rich Water in the Kangwon Province)

  • 최현수;고용권;김천수;배대석;윤성택
    • 자원환경지질
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    • 제33권6호
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    • pp.491-504
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    • 2000
  • Environmental isotope $^{18}O$, $^{2}H$, $^{3}H$,$^{13}C$, $^{34}S$and $^{87}Sr/^{86}Sr$) studies on ${CO_2}$-rich waters in the Kangwon Province were carried out to elucidate the origin, residence time, water-rock interaction and mixing process of their. ${\delta}^{18}O$ and ${\delta}D$ data indicate that ${CO_2}$-rich waters were derived from the local meteoric water. It also shows that each type of ${CO_2}$-rich water has distinct isotopic composition and Na-${HCO_3}$ type water (-10.8 to -12.1${\textperthousand}$, ${\delta}^{18}O$ ) is lighter than other type waters. These depleted isotopic values supposedly indicate that, considering the altitude effect of isotope in Korea, the recharge area of Na-${HCO_3}$ type water can be estimated to be relatively higher in elevation than those of Ca-${HCO_3}$ and Ca-Na-${HCO_3}$ type waters. Tritium contents close to zero are observed in the Na-${HCO_3}$ type water, confirming a long residence time and the possibility of a ${CO_2}$ inflow into the aquifer at great depth. These isotope data also show that the Ca-${HCO_3}$ type water has undergone mixing process with surface water during ascending at depth, whereas Na-${HCO_3}$ type water was less mixed with surface waters. The carbon isotope data (-8.8 to +0.8 ${\textperthousand}$ ${\delta}^{13}C$) indicate that dissolved carbon in the ${CO_2}$-rich waters was possibly derived from deep seated ${CO_2}$ gas. The high ${\delta}^{34}S$ values (up to 38.1${\textperthousand}$) of dissolved sulfates suggest that sulfate reduction by microbial activity had occurred at depth. Strontium isotopic data ($^{87}Sr/^{86}Sr$) of ${CO_2}$-rich waters indicate that the chemistry of the ${CO_2}$-rich waters is determined by water-rock (granite) interaction.

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Solubility of TiO2 in NaF-CaF2-BaF2 Melts

  • Yoo, Jeong-Hyun;Cho, Sung-Wook
    • Metals and materials international
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    • 제24권6호
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    • pp.1386-1393
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    • 2018
  • The solubility of $TiO_2$ in $NaF-CaF_2-BaF_2$ ternary eutectic melts was investigated at the temperature range of $1025-1150^{\circ}C$. The least-squares equation was obtained from the relationship between the reciprocal temperature and the natural logarithm of the titanium concentration in the melts saturated with $TiO_2$. The corresponding partial molar enthalpy of dissolution of $TiO_2$ was found to be 188 kJ/mol. The titanium saturation concentration was 3.73 wt% at $1100^{\circ}C$. From the titanium concentration change with the added amount of $TiO_2$ at different holding time after a final stirring, it was found that not only complete dissolution of $TiO_2$ but also enough sedimentation of excessive $TiO_2$ should be guaranteed to obtain more reliable solubility data. The holding time of 10 h was found to be enough for the excessive $TiO_2$ particles to settle down in our experimental conditions. It is noteworthy that in case of adding $TiO_2$ in excess of its solubility, the $Ba_{1.12}(Ti_8O_{16})$ phase was observed at the lower and bottom of the solidified salt ingots.

2.45 GHz 전자기파 조사하에서 Aluminum Borate Whisker의 성장 거동 (Growth Behavior of Aluminum Borate Whisker under 2.45 GHz Electromagnetic Irradiation)

  • 김성완;이상근;김지경;이창희;안진모;신준식;박성수;박희찬
    • 한국세라믹학회지
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    • 제40권10호
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    • pp.998-1004
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    • 2003
  • 두 종류의 출발물질인 $Al_2$(S $O_4$)$_3$+x$Na_2$B$_4$ $O_{7}$$.$10$H_2O$(몰비;x=0.1, 0.7)와 ${\gamma}$-Al$_2$ $O_3$+x$Na_2$B$_4$ $O_{7}$$.$10$H_2O$(몰비; x=0.1, 0.7) 혼합시료로부터 재래식 및 마이크로파 열처리를 행하여 휘스커형 $Al_{18}$B$_4$ $O_{33}$ 입자들을 합성하였다. 휘스커형 $Al_{18}$B$_4$ $O_{33}$ 입자들의 성장에 마이크로파, flux양 및 온도의 영향을 X-선 회절장치 및 주사형 전자현미경을 사용하여 조사하였다. 재래식 및 마이크로파 열처리된 두 종류의 혼합시료는 각각 온도 및 flux양이 증가할수록 휘스커형 $Al_{18}$B$_4$ $O_{33}$ 입자의 크기가 증가하는 경향을 나타내었다. 한편, 재래식 열처리된 시료에 비하여 마이크로파 열처리된 시료에서 휘스커형 $Al_{18}$B$_4$ $O_{33}$ 입자들이 잘 발달되었다.자들이 잘 발달되었다.