• 제목/요약/키워드: Hydrogen ion concentration

검색결과 235건 처리시간 0.026초

자라에서 본 관류액(灌流液) pH와 심장박출량(心臟搏出量) (Cardiac Performance of Turtle Heart in Various pH of Perfusate)

  • 양일석
    • The Korean Journal of Physiology
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    • 제9권1호
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    • pp.69-76
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    • 1975
  • Cardiac performances were analyzed in intact turtle heart(Amyda japonica), perfusing with turtle Ringer-Locke's solution containing various hydrogen ion concentration, at several levels of arterial and venous pressure. 1. Ventricular work increased when venous pressure, or venous filling pressure increased, and also increased when arterial pressure increased. 2. The higher the arterial pressure, the lower the cardiac to output, for arterial pressure is the resistance to the ventricular blood flow. On the other hand, in specific arterial pressure, cardiac output was proportional to the venous filling pressure. 3. Heart rates did not change significantly during the perfusion with Ringel· solution of various pH. 4. In the heart Perfused with Ringer solution of various pH, ventricular work was the highest at PH 7.6 (at 6 $cmH_2O$ arterial pressure and 8 $cmH_2O$ venous pressure, the ventricular work was 63.09m$\cdot$cm). However, within the range of pH $7.1{\sim}7.6$, there were no significant changes in cardiac output and ventricular work. Below the level of pH 7.0, ventricular work decreased to less than 56% of maximium value (at $6cmH_2O$ arterial pressure and $8cmH_2O$ venous Pressure, ventricular work was 36.0$gm{\cdot}$ at pH 7.0). At pH 7.7 ventricular work decreased to less than 48% of maximum value (ventricular work: 30.0 $gm{\cdot}$). The nature of the cardiac performance at the various arterial and venous pressures was similar to that of normal heart. 5. Turtle heart seemed to be relatively insensitive to acid-base disturbances. The mechanism of negative inotropic effect of hydrogen ion was discussed.

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수소크롬산 이온에 의한 옥살라토아쿠아몰리브덴(IV) 삼합체의 산화반응 (Kinetic Studies on the Oxidation of Oxalatoaquamolybdenum(IV) Trimer by Hydrogen Chromate Ion)

  • 김창수;권창룡
    • 대한화학회지
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    • 제30권1호
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    • pp.57-62
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    • 1986
  • HCr$O_4^-$에 의한 $[Mo_3O_4(C_2O_4)_3(H_2O)_3]^{2-}$의 산화는 몰리브덴(IV)화합물, $[Mo_2O_5(C_2O_4)_2(H_2O)_2]^{2-}$를 생성한다. HCr$O_4^-$$[Mo_3O_4(C_2O_4)_3(H_2O)_3]^{2-}$의 반응에 대한 화학양론은 $2Mo_3^{IV} + 4Cr^{VI} {\to} 3Mo_2^{VI} + 4Cr^{III}$와 같다. 관찰된 속도상수는 수소이온농도에 의존한다.$Cr^{VI}$$Cr^V$$Cr^{IV}$를 거쳐서 $Cr^{III}$로 일전자씩 연속적으로 변화한다. 상세한 메카니즘이 논의된다.

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건설폐기물 분리매립 및 생활폐기물과의 혼합매립에 의한 매립가스 발생 특성 (Characteristics of Landfill Gas Generation by Separate Landfill of Construction Waste and Mixed Landfill with Household Waste)

  • 박종근;천승규
    • 신재생에너지
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    • 제18권4호
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    • pp.1-11
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    • 2022
  • Landfill gas (LFG) generation characteristics in a construction waste landfill zone (block E) and mixed landfill zone (block A) were analyzed. During the period from October 2018 to April 2022, a total of 936×103 and 1,001×103 tons of waste were disposed in block E and block A, respectively. Out of this, 27.1% and 55.6% were biodegradable waste in block E and block A, respectively. The landfill masses of the two blocks were converted to be comparable. Then, the biodegradable waste and organic carbon were estimated by element analysis, biodegradable carbon by biochemical methane potential experiment (DC), and sulfate ion by acid decomposition. Results showed that biodegradable waste, organic carbon, biodegradable carbon, and sulfate ions in block A were 2.1, 1.6, 5.2, and 0.4 times greater than those in block E, respectively. The amount of LFG generated by block A was 4.8 times greater than that by block E. The average concentrations of methane (CH4) were 60.8% and 60.9% in block E and block A, respectively, which were unrelated to the nature of disposed waste. The average concentrations of hydrogen sulfide (H2S) were significantly high in block E (4,489 ppm) and block A (8,478 ppm). As the DC/SO42- of block E and block A were 0.35 and 4.56, respectively, increase in DC/SO42- caused increase in not only the total amount but also the concentration of H2S generated.

Polarography에 依한 Cupric-thiocyanate의 Kinetics와 Cuprous-thiocyanate의 Adsorption Wave에 關한 硏究 (Polarographic Studies on the Kinetics of Cu(II)-thiocyanate and the Adsorption Wave of Cu(I)-thiocyanate)

  • 황정의;정종재;손무용;박유철
    • 대한화학회지
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    • 제14권3호
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    • pp.213-219
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    • 1970
  • In the presence of hydrogen peroxide, the effects of temperature and pH to the catalytic reaction velocity of cupric -thiocyanate and the quantities of reduction products adsorbed on the D.M.E. have been studied by polarographic method. According to these experiments, the following empirical equation has been derived for the relation among temperature $T_i$, concentration of hydrogen ion $pH_i$ and adsorbed cuprous-thiocyanate in moles/$cm^2Z_{ij}$, and rate constant log$K_{ij}$ $$log\;K_{ij}=\frac{1}{T_i}\{A(pH_j)+B\}+C(pH_j)+D$$ $$Z_{ij}=\frac{1}{T_i}\{{\alpha}(pH_j)^{\frac{1}{2}}+{\beta}\}+{\gamma}(pH_j)^{\frac{1}{2}}+{\delta}$$ where, A,B,C,D and {$\alpha},{\beta},{\gamma},{\delta}$ are constants. The Calculated values by both equations are well agreed with empirical values within 8% in the error.

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A comparison of traditional and quantitative analysis of acid-base and electrolyte imbalance in 87 cats

  • Chun, Daseul;Yu, DoHyeon
    • 대한수의학회지
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    • 제61권4호
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    • pp.40.1-40.6
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    • 2021
  • Acid-base disorder is a common problem in veterinary emergency and critical care. Traditional methods, as well as the Stewart method based on strong ion difference concepts and the Fencl-Stewart method, can be used to analyze the underlying causes. On the other hand, there are insufficient comparative study data on these methods in cats. From 2018 to 2020, 327 acid-base analysis data were collected from 69 sick and 18 healthy cats. The three most well-known methods (traditional method, Stewart method, and Fencl-Stewart method) were used to analyze the acid-base status. The frequency of acid-base imbalances and the degree of variation according to the disease were also evaluated. In the traditional acid-base analysis, 5/69 (7.2%) cats showed a normal acid-base status, and 23.2% and 40.6% of the simple and mixed disorders, respectively. The Fencl-Stewart method showed changes in both the acidotic and alkalotic processes in 64/69 (92.8%), whereas all cats showed an abnormal status in the Fencl-Stewart method (semiquantitative approach). The frequencies of the different acid-base imbalances were identified according to the analysis method. These findings can assist in analyzing the underlying causes of acid-base imbalance and developing the appropriate treatment.

일치환 Bezaldehyde 의 Semicarbazone 생성 반응에 관한 연구 (Studies on the Semicarbazone Formation of Mono substituted Benzaldehydes)

  • 김용인;김창면
    • 한국응용과학기술학회지
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    • 제7권1호
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    • pp.93-105
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    • 1990
  • Semicarbazone formation of nine monosubstituted benzaldehydes was studied kinetically in 20% methanol buffer solution at 15, 25, 35, and $45^{circ}C$. The rate of p-nitrobenzaldehyde semicarbazone formation is 2.7 times as fast as that of benzaldehyde, while p-hvdroxybenzaldehyde is 3.6 times as slow as that of benzaldehyde. Activation energies for p-chlorobenzaldehyde, benzaldehyde, p-methylbenzaldehyde, p-methoxybenzaldshyde, p-hydroxybenzaldehyde, and p-dimethylaminobenzaldehyde semicarbazone formation are calculated as 5.80, 6.19, 6.57, 7.06, 8.03, and 6.46 kcal/mol respectively. It is concluded from the effect of ionic strength that the reaction is affected by not ions but neutral molecules involving hydrogen bonding between oxygen atom of carbonyl group and hydrogen atom of acid-catalyst, and concerted attack of the necleophilic reagent, free base on carbonyl compound. Also, the effect of solvent composition is small in 20% and 50% methanol (and ethanol) aqueous solutions. The ${\rho}-{\sigma}$ plots for the rates of semicarbazone formation at pH 7.1 show a linear ${\rho}-{\sigma}$ relationship (${\rho}=0.14l$, in contrast to that at pH 2.75 and pH 5.4 corresponding to ${\rho}-{\sigma}$ correlations reparted by Jencks. The rate of semicarbazone formation at pH 5.4 show a relationship which is convex upward, resulting in a break in the curve but at pH 2.75, slight difference from a linear relationship. As a result of studying citric acid catalysis, second-order rate constants increase linearly with citric acid concentration and show a 2 times increase as the catalyst concentration is varied from 0.025 to 0.1 mol/1 at pH 2,9, but slight increase at pH 5.3. The rate-determining step is addition below pH 5 but is dehydration between pH 5 and 7. Conclusively, the rate-determining step of the reaction changes from dehydration to addition in respect to hydrogen ion activity near pH 5. The ortho: para rate ratio of the hydroxybenzaldehydes for semicarbazone formation is about 17 at $15^{\circ}C$. It is concluded that the results constitute strong evidence in favor of greater stabilization of p- than o-hydroxybenzaldehyde by substituent which donate electrons by resonance and is due to hydrogen bonding between the carbon-bound hydrogen of the-CHO group and the oxygen atom of the substituent.

칼슘 페라이트 이온-선택성 막전극 (Ion-Selectrodes based on Calcium Ferrite)

  • 김정희
    • 분석과학
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    • 제5권4호
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    • pp.401-408
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    • 1992
  • 산화칼슘과 산화철을 0.6:1.4, 0.8:1.2, 1.0:1.0 몰비로 혼합하여 만든 디스크 형태의 시편들을 $1400^{\circ}C$ 산소 분위기와 수소 분위기하에서 각각 소결하였다. 수소 분위기하에서 만든 calcium ferrite 막전극이 산소 분위기하에서 만든 calcium ferrite 막전극 보다 더 우수한 감응전위와 감응농도범위를 나타냈다. 수소 분위기하에서 만든 calcium ferrite ($CaO:Fe_2O_3=0.6:1.4$ 몰비) 막전극은 $Ca^{2+}$, $Ba^{2+}$, $Mg^{2+}$, $Zn^{2+}$와 같은 2가 금속 양이온과 $I^-$, $Br^-$와 같은 할로겐 음이온에 대하여 Nernstian 기울기에 근접한 높은 감응전위를 나타내었다.

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산성-산화성 분위기에서 니켈(Ni), 코발트(Co) 및 은(Ag) 이온의 연속식 이온교환 특성 (Continuous Ion Exchange Characteristics of Ni, Co and Ag Ions in Acidic-Oxidizing Conditions)

  • 김영호;양현수;김웅기
    • 공업화학
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    • 제10권2호
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    • pp.218-224
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    • 1999
  • 원자로 정지시 혼상 탈염기의 최적 운전방법을 제안할 목적으로 산성-산화성 분위기에서 저농도의 Ni, Co 및 Ag 이온이 함유된 모의 냉각재 용액의 연속식 이온교환특성을 연구하였다. 금속 이온의 제거 용량에 미치는 양이온 교환수지 형태의 효과로서 $H^+$형 수지의 성능은 $Li^+$형 수지의 성능보다 약 6% 정도 높은 것으로 나타났다. 혼합층 이온교환 방법인 양이온과 음이온 수지의 혼합은 비혼합시와 비교하여 금속 이온들의 제거 용량에는 영향을 미치지 않았으나 금속 이온들의 파과곡선의 기울기를 매우 조금 증가시켰다. 냉각재의 산성-산화성 분위기와 관계된 영향으로서 붕산의 첨가는 금속 이온들의 파과곡선의 기울기를 매우 작게 감소시킨 반면, 과산화수소의 첨가는 금속이온들의 제거 용량을 약간 감소시켰다.

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식품가공폐유를 이용한 비누의 계면활성과 세척성에 관한 연구 (A Study on the Surface Activity and Detergency of the Soap Made from the Waste Oil from Food Manufacturing Proces)

  • 정명섭;유덕환
    • 한국의류학회지
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    • 제18권5호
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    • pp.661-673
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    • 1994
  • We have gathered a fatty acid to recycle the waste oil of food manufacturing process, and then made a soap from the waste oil by alkali saponification. Effects of the washing elements such as the concentration of the soap, temperature and time were evaluated to find out the optimum washing conditions, and results are as follows. 1. We could find soaps made from the soybean oil (A), corn oil (B), rape seed salad oil (C), cotton seed oil (D) and a soap consisting of the each oil 25% respectively (I) had the lowest surface tension at the concentration of 0.225% -0.25%. Compared with the single fatty-acid soap, the multi-component soap I showed the lower surface tension at the cmc. 2. All the samples of A-I showed the lowest contact angle for the solid material at the concentration of 0.25%. The multi-component soap of I showed higher contact angle than the single.component soaps of A, B, C and D. 3. The soap G, made from the waste oil, show lower surface tension than 5, made from the complex raw fats of the eatable fatty oil acid and H, commercial soap. 4. The washing efficiency depends on the washing time. Especially the 25-minute was found to be the optimum washing time. 5. The highest washing efficiency was found at the 0.25% cont. reagardless of the washing temperature. At 0.15% concentration level the washing efficiency reduces as washing tem- perature increases. At 0.3% concentration level the highest washing efficiency was found between $50^{\circ}$-$60^{\circ}$. 6. The soap made from the waste oil showed the highest washing efficiency in terms of concentration, temperature, and time. 7. The soap made from the waste oil showed the similiar concentration of hydrogen ion to the synthetic detergent. 8. The hand value of the fabric washed by the soap made from the waste oil was a little lower value than those washed by the synthetic detergent.

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사질토양에서의 pH조건에 따른 Zn의 이동특성 (Transport of Zn Ion under various pH Conditions in a Sandy Soil)

  • 박민수;김동주
    • 대한환경공학회지
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    • 제22권1호
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    • pp.33-42
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    • 2000
  • 중금속은 토양 내에서 비보존성 화학물질로 작용하므로 흡착에 의해 지연효과가 발생할 수 있고 흡착은 pH에 영향을 받는다고 보고된 바 있다. 그러므로 토양 및 지하수 오염을 예방하고 복구하기 위해서는 다양한 pH조건에서 중금속의 이동형태를 파악하는 것이 중요한 연구과제가 된다. 본 연구에서는 사질토양에서 pH에 따른 중금속의 이동특성을 연구하기 위하여 배치실험과 주상실험올 수행하였다. 배치실험의 경우 초기농도별로 11가지의 $ZnCl_2$ 40 mL 용액과 사질토양 10g을 교반기에서 72시간 반응시켜 평형상태에 도달하게 한 후 용액을 채취하여 Zn, Ca, Mg의 세 가지 양이온을 ICP-AES로 분석하였다. 주상실험은 3가지 pH조건 (7.7, 5.8, 4.1)에서 10 g/L의 KCl과 $ZnCl_2$를 추적자로 사용하여 순간주입 (pulse injection) 형태로 토양시료 상부에 투입한 후 Time Domain Reflectometry (TDR)를 사용하여 10 cm 깊이에서 잔존수농도를, EC-meter와 ICP분석을 통하여 20 cm 깊이의 하부 경계면에서 침출수농도를 분석하였다. 배치실험 결과, Zn은 Ca, Mg와 이온교환의 형태로 흡착이 발생하였고 등온 흡착방정식의 각 모델 (Linear, Freundlich, Langmuir)별로 최저 1.2에서 최고 614.1의 지연계수를 나타냈다. 주상실험에서도 모든 pH조건에서 Zn이온이 이온교환을 하여 흡착이 발생하였으나, 잔존수와 침출수 형태의 파과곡선 모두에서 Zn이용의 첨두농도 도달시간이 K이온과 일치하여 지연효과는 발생하지 않은 것으로 나타났다. 이는 정상류 상태로 부과한 낮은 배경농도의 용탈수내에 Zn보다 강한 이온교환능을 가지는 원소가 존재하지 않아 Zn의 탈착이 발생하지 않았기 때문이다. pH가 낮을수록 Zn는 용액내 수소이온 ($H^+$)의 증가로 치환능이 감소하여 첨두농도가 높게 나타났고, 상대적으로 치환되는 Ca, Mg의 양은 줄어들었다. 따라서 본 연구에 적용된 배치실험과 주상실험의 조건하에서는 Zn이온이 이온교환반응에 의한 흡착이 발생하였으나 지연효과는 발생하지 않았고 가장 낮은 pH에서 첨두농도가 최고 12.7배까지 증가하였다.

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