• Title/Summary/Keyword: 산과염 용액

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Effect of Coions on the Absorption of rare Earths in a Cation Exchange Resin (양이온 교환수지에 대한 희토류 원소의 흡수에 미치는 Coion의 영향)

  • Beom-Gyu Lee;In-sook Kim;Kang-Jin Kim
    • Journal of the Korean Chemical Society
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    • v.27 no.1
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    • pp.18-23
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    • 1983
  • To understand the abnormal absorption behavior of rare earths in cation exchange resins, the absorption for Ce(III), Tb(III) and $Cl^-$ ions in Dowex 50W-X2 have been investigated by spectrophotometry in the concentration range of $1{\sim}12$ M HCI and $HCl-HClO_4$ mixed solutions. The amount of $Cl^-$ ion absorbed shows that the ratio of amount of $Cl^-$ ions to that of rare earths does not exceed 10% in the concentration range of $6{\sim}8M$ HCl and decreased gradually to 3% at 2M HCl and 6% at 12M HCl. The ratio is further decreased with the fraction of $HClO_4$ in $HCl-HClO_4$ mixed solutions and the decrease is presumably due to the weak tendency to form a complex between rare earths and $Cl^-$ ions in a cation exchange resin. The effect of $ClO_4^-$ is expected to play a more important role than that of $Cl^-$ ions in the large absorption of rare earths.

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Study on the Elution Behaviors of Molybdate and Tungstate in Nitric Acid Solution by Anion Exchange Chromatography (음이온 교환수지에 의한 질산산성에서 몰리브덴산과 텅스텐산의 용리현상에 관한 연구)

  • Ki-Won Cha;Jae-Seong Choi
    • Journal of the Korean Chemical Society
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    • v.28 no.1
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    • pp.54-61
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    • 1984
  • The species and equilibrium of molybdate and tungstate have been investigated from the elution behaviors of those in various concentrations of nitric acid and the UV spectra obtained at the various Z values. In higher concentrations than 0.05M nitric acid, the nitarte complex species of $MoO_2(NO_3)_2$ seems to form from the $MoO_2^{2+}$ ions formed by the following equation: $Mo_8O_{26}^{4-} + 20H^+$ ${\rightleftharpoons}$ $8MoO_2^{2+}$ + $10H_2O$. In the case of tungstate, the elution behaviors of tungstate in nitric acid medium are similar to those of perchloric acid, so we think the equilibrium of tungstate existed in perchloric acid could be also existed in nitric acid. These elution behaviors of tungstate are compared with the UV spectra obtained at the various Z values.

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Investigation on the spectroscopic characteristics for Pu oxidation state in acid and alkali medium (산 및 알칼리 매질에서 Pu 산화수에 대한 분광학적 특성 조사)

  • Lee, Myung-Ho;Kim, Jong-Yun;Kim, Won-Ho;Jung, Euo-Chang;Jee, Kwang-Yong
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.5 no.2
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    • pp.103-108
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    • 2007
  • The absorption spectra of Pu in stock solution were measured using a UV-Vis-NIR spectrophotometer after dissolving $PuO_2\;with\;HNO_3$, HF and $HClO_4$. The spectroscopic characteristics of Pu (III, IV, VI) in acidic, neutral and alkali media were investigated. Also, the intensities and position of major peaks for Pu(VI) were observed with increasing acidic and alkali concentration. The variation of oxidation states of Pu(VI) with an adding reducing reactant was investigated in HCl and NaOH medium.

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Kinetics and Mechanism of the Hydrolysis of Enol Ester in Strong Acidic Solution (강산성용액에서 엔올에스테르의 가수분해에 대한 반응속도론적 연구)

  • Heo, Tae Seong;Yu, Gyeong Hwa
    • Journal of the Korean Chemical Society
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    • v.38 no.5
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    • pp.391-396
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    • 1994
  • The hydrolysis of $\alpha-benzoxystyrene(1)$ in strong acidic solution has been investigated kinetically. In perchloric acid concentration lower than 5.5 M($H_o$ < -3.0), hydration paramer $\omega$ = + 7.6, and $\Phi$ = + 0.54 were obtained. The solvent isotope effect $k_{H_2O}/K_{D_2O}$ is 0.72. The substituent effect was found to conform to the Hammett $\sigma^+$ constant with $\rho$ = -0.60. On the basis of these results and other evidence, the hydrolysis of the enol ester proceeds by $A_{AL}$2 type mechanism. In concentration greater than 5.5 M($H_o$ > -3.0), isotope effect, $k_{H_2O}/_{D_2O}$ is 3.32, substituent effect, $\rho$ is -1.60 and the rate is linear with the acidity function, $H_o$. Thus, the mechanism changes one involving initial, and rate-determining olefin protonation.

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Effects of Salts and Acid Solutions on the Weathering of Granite (화강암의 풍화에 미치는 염분과 산성용액의 영향)

  • Shon, Byung-Hyun;Jung, Jong-Hyeon;Kim, Hyun-Gyu;Yoo, Jeong-Gun;Lee, Hyung-Kun
    • Journal of Korean Society of Environmental Engineers
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    • v.27 no.1
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    • pp.101-108
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    • 2005
  • Because the stone cultural properties located outdoors, they have been altered and deteriorated in external appearance due to environmental factors such as acid rain, extreme change in temperature, and salts. Damage to stone cultural properties is accelerated particularly due to recent industrial development and environmental pollution. An experimental study was conducted to evaluate the effect of environmental contaminants on the weathering of granite. And as part of the developing of conservation method, $TiO_2$ catalyst was prepared and tested. When fresh granite was dipped into the salt and acid solutions, dissolution rate of eight minerals (Si, Mg, Ca, Na, K, Fe, Mn, Al) are abruptly increased at initial stage of reaction and then increased steadily until 100 cycles. After salt and acid solution experiments, the mineral compositions of the granite surface were lower then that of the fresh granite and density of the weathered granite was steadily decreased from $2.60\;g/cm^3$ to $2.56\;g/cm^3$, but Poissions ratio and absorption ratio were slightly increased. It was expected at stone cultural assets could be weathered by salts and acid rain. In the case of $TiO_2$ was coated to the granite, the dissolution rate of minerals and absorption ratio of $TiO_2$ coated granite were decreased. Therefore, the $TiO_2$ coating method tested in this study considered to be a viable method to assist in the conservation of stone cultural properties from environmental contaminants.