• 분석과학
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• 제14권6호
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• pp.530-534
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• 2001

Effect of stripping solutions on the Duolite GT-73 chelating resin for ten elements, Ag(I), Al(III), Ca(II), Cd(II), Cu(II), Fe(II), Hg(II), Mn(II), Pb(II), and Zn(II), was investigated. Relation between affinities of the metal ions and solubility products of metal sulfides was studied. The smaller the solubility product of metal sulfideis, the larger the affinitie with the ionsis. The ions which have the solubility products larger than $10^{-23}$ could be effectively desorbed with nitric acid. Complexation with chloride ion enhanced the desorption efficiencies of the ions having moderately strong affinity with the resin. The ions which have very strong affinity by the chelating resin can be desorbed by complextion with thiourea and hydrochloric acid.

• 한국산업보건학회지
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• 제30권2호
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• pp.87-98
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• 2020

Objective: The purpose of this study was to propose a sequential procedure for the simultaneous analysis of soluble and insoluble metal compounds. Methods: Methods for sampling and analyzing metal compounds such as ISO standards, NIOSH methods, HSE methods, and OSHA methods were reviewed. Results: Some metals have different OELs depending on the solubility of the compound. Therefore, we should take into account these characteristics and perform an exposure assessment. Soluble metal compounds are first extracted from the filter, and then the filter is digested by acids to analyze residual insoluble components. The extraction of soluble compounds can be completed by agitation for about 60 minutes with a leach solution (water) in a water bath at 37℃. For the analysis of insoluble compounds, the sample filter and the filtration filter remaining after the extraction of the soluble compounds are analyzed. This allows simultaneous determination of soluble and insoluble metal compounds. For hexavalent chromium compounds, soluble hexavalent chromium can first be extracted from the filter by using sulfate buffer. The insoluble hexavalent chromium remaining in the filter can then be extracted using carbonate buffer. Conclusion: Workers are often exposed to many hazardous substances with different exposure limits at industrial sites. The OELs for compounds of the same metal can be set differently depending on solubility. This study can help evaluate a worker's exposure to metal compounds by suggesting methods for the simultaneous determination of soluble and insoluble metal compounds.

• 한국세라믹학회지
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• 제28권2호
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• pp.130-140
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• 1991

The powders of the system Si3N4-Y2O3-AlN were prepared using Si(OC2H5)4 and YCl3.6H2O together with commercial AlN powder. $\alpha$-Si3N4 was prepared by the carbothermal reduction and nitridation of the hydrolyzed gel at 135$0^{\circ}C$ for 10h in N2 atmosphere. YCl3.6H2O was observed to be changed to Y2O3 during the reaction. $\alpha$-Sialon(X=0.2, 0.4, 0.6) ceramics were obtained by hot-pressing the Si3N4-Y2O3-AlN mixture at 178$0^{\circ}C$ for 1h under 30 MPa. The content of $\alpha$-Sialon increased with increasing metal solubility(x value) and $\alpha$-Sialon single phase was obtained at the metal solubility of 0.6. With increasing metal solubility, flexural strength, fracture toughness and thermal shock resistence were decreased, while the microhardness was increased. Large elongated $\beta$-Si3N4 grains were mainly observed at lower metal solubility. Mechanical prorerties of the sintered ceramics with X=0.2 were measured as follows : flexural strength ; 650 MPa, fracture toughness ; 3.63 MN/m3/2, hardness ; 14.7 GPa, thermal shock resistence temperature ; 58$0^{\circ}C$.

• Corrosion Science and Technology
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• 제7권4호
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• pp.237-242
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• 2008

Physical properties of water, such as dielectric constant and ionic product, significantly vary with the density of water. In the supercritical conditions, since density of water widely varies with pressure, pressure has a strong influence on physical properties of water. Dielectric constant represents a character of water as a solvent, which determines solubility of an inorganic compound including metal oxides. Dissociation equilibrium of an acid is also strongly dependent on water density. Dissociation constant of acid rises with increased density of water, resulting in drop of pH. Density of water and the density-related physical properties of water, therefore, are the major governing factors of corrosion and environmentally assisted cracking of metals in supercritical aqueous solutions. This paper discusses importance of "physical properties of water" in understanding corrosion and cracking behavior of alloys in supercritical water environments, based on experimental data and estimated solubility of metal oxides. It has been pointed out that the water density can have significant effects on stress corrosion cracking (SCC) susceptibility of metals in supercritical water, when dissolution of metal plays the key role in the cracking phenomena.

• 한국표면공학회지
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• 제23권4호
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• pp.225-229
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• 1990

Solubility Products of metal oxides, such as Al2O3 and UO2 in KCl-LiCl eutectic composition was calculated by using an exact an exact thermodynamic. The values for Al2O3 ThO2 and UO2 were found to be 2.51$\times$10-27, 4.97$\times$10-15and 2.17$\times$10-12in mole per liter basis at 743 K, respectively. The correlation of theoretical values with those of experiment were in good agreement. It is worth to note that the exact cycle method was proved to be satisfactory in making predictions of solubillities and also solubility products of sparingly soluble metal oxides in an ionic salt system.

• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2454-2458
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• 2007

Exploring the basic concepts for the design of CO2-philic molecules is important due to the possibility for “green” chemistry in supercritical CO2 as substitute solvent systems. The Lewis acid-base interactions and C?H…O weak hydrogen bonding were suggested as two key factors for the solubility of CO2-philic molecules. We have performed high level quantum mechanical calculations for the van der Waals complexes of CO2 with trimethylphosphate and trimethylphosphine oxide, which have long been used for metal extractants in supercritical CO2 fluid. Structures and energies were calculated using the MP2/6-31+G(d) and recently developed multilevel methods. These studies indicate that the Lewis acid-base interactions have larger impact on the stability of structure than the C?H…O weak hydrogen bonding. The weak hydrogen bonds in trimethylphosphine oxide have an important role to the large supercritical CO2 solubility when a metal is bound to the oxygen atom of the P=O group. Trimethylphosphate has many Lewis acid-base interaction sites so that it can be dissolved into supercritical CO2 easily even when it has metal ion on the oxygen atom of the P=O group, which is indispensable for a good extractant.

• 한국토양환경학회지
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• 제5권3호
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• pp.55-64
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• 2001

많은 유기 염소계 농약들은 환경에서 매우 지속적이며, 먹이 사슬을 통해서 중요하게 생물학적으로 농축하는 경향이 있다. 농업에 적용되는 농약은 지표수의 유출이나 지하수의 흐름을 통해서 사실상 수 계로 이동되어지기 때문에 수환경에 특히 많은 영향을 끼치게 된다. 이 논문의 연구 목적은 두 가지 다른 휴믹산에 의한 유기 염소계 농약인 lindane과 dieldrin의 수중 용해도 증가에 중금속인 납 이온이 미치는 영향에 대해 알아보고자 하는 것이다. 또한 유기 염소계 농약이 두 가지 혼합물로 존재할 때 각각의 용해도에 서로의 상호작용에 대해서도 연구해 보고자 하였다. 휴믹산에 의한 lindane의 용해도 증가 정도는 거의 일정하였지만, 이에 비해 휴믹산에 의한 dieldrin의 수중 용해도 증가는 훨씬 증가함을 보여주었다. 또한 수중에 휴믹산과 납이 공존하면 dieldrin의 용해도는 납이 존재하지 않을 때보다 더욱 감소하였다.

• 한국토양비료학회지
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• 제40권4호
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• pp.280-291
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• 2007

토양중 중금속을 흡수해서 체내에 고농도로 축적할 수 있는 식물, 이른바 고축적식물(hyperaccumulator)의 발견으로 오염토양에 대한 식물복원(phytoremediation) 기술에 대한 많은 연구들이 수행되고 있다. 이들 연구의 방향은 크게 고축적식물의 중금속 축적 기작을 밝히기 위한 것과 축적효율을 높임으로써 복원 효율을 향상시키는 실용적인 기술개발로 나누어진다. 지금까지 고축적식물에 의한 중금속 축적 기작은 다섯 가지의 특이 기작으로 알려져 있는데, 1) 뿌리세포의 중금속 흡수 증진, 2) 식물체 조직내의 중금속 이동성 향상, 3) 중금속의 무독화(detoxification) 및 격리(sequestration), 4) 토양-뿌리 경계면에서의 중금속 유효도 증진, 그리고 5) 중금속 오염토양으로의 능동적인 뿌리의 성장 등이 이에 속한다. 일반적으로 토양 중 낮은 중금속 유효도는 식물복원 기술의 현장 적용에 있어 제한요소로 간주된다. 이를 극복하기 위해서는 위에 기술된 다섯 가지 기작 중 고축적식물의 뿌리가 근권 토양중 중금속의 화학변화에 미치는 영향을 이해하는 것이 매우 중요하다. 식물 뿌리에 의한 근권 토양의 pH 변화와 뿌리에서 나오는 분자량이 적은 유기산(low-molecular-weight organic acids, LMWOAs)과 같은 유기성 분비물은 근권부 토양의 화학적 특성을 변화시키고 결과적으로 중금속의 유효도를 변화시킨다. 예를 들어 뿌리에서 나오는 $H^+$ 이온은 토양 pH를 감소시키고 이에 따라 중금속의 유효도는 증가한다. 또한 고농도의 중금속에 노출된 뿌리는 많은 양의 유기물질을 분비하게 되고 근권 토양에 축적되는 이 유기물질은 토양중 중금속과 결합하여 유기복합물질(organo-metallic complexes)을 형성하면서 유효도를 증가시킨다.

• 한국세라믹학회지
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• 제51권4호
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• pp.312-316
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• 2014

The joining behavior of forsterite ceramics to SUS304 alloy using $8PbO-78Bi_2O_3-8B_2O_3-4ZnO-2SiO_2$ (wt%) system glass frit was investigated. The contact angle was smaller than $90^{\circ}$ at a temperature of $460^{\circ}C$. Redox reaction at the interface between forsterite and SUS304 was found to appear when the electrons in the metal part moved toward the glass part and the oxygen ions in glass moved to the metal side. The decrease of the surface tension due to the PbO solubility on the forsterite side contributed to the better wetting behavior at low temperature.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.353-356
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• 2001

The relation between the flocculation and dispersion of metal oxide powders and the properties of solvents, such as dielectric constant and solubility parameter, was investigated for TiO$_2$, $Al_2$O$_3$and Fe$_2$O$_3$particles. The particle size and median diameter of these metal oxides were measured in many organic solvents, from which the effect of solvents on the flocculation and dispersion of metal oxide powders was considered. The metal oxide powders of TiO$_2$, $Al_2$O$_3$and Fe$_2$O$_3$tend to disperse in a solvent of higher polarity, whereas they are apt to flocculate in a solvent of low dielectric constant, because the Hamaker constant between the particles becomes larger in such a solvent. There we, however, some solvents that do not obey these tendencies. It is possible to evaluate the flocculation and dispersion of these metal oxide powders in many solvents by using numeral balances of Hansen’s three-dimensional solubility parameter (f$_{d}$, f$_{p}$ and f$_{h}$). There exists a solvent giving the optimal dispersion for each metal oxide, and the optimal dispersion point of f$_{d}$, f$_{p}$ and f$_{h}$ is determined by the combination of various metal oxide powders and solvents.nts.nts.nts.