• Bulletin of the Korean Chemical Society
• /
• v.21 no.8
• /
• pp.801-804
• /
• 2000

A crossed beam scattering of a $Pb(ZrxTi1-x)O_3plume$ and an oxygen jetwas studied by using a time-of-flight quadrupole mass spectroscopy. Both simple collisions and reactive scatterings had significant effects on the transportand energetics of ions in the plume. Relative enrichment of metal and metal oxide ions was also changed with the oxygen pulse because of the differences in the mass and chemical properties of the ions. In particular, an anomalous increase ofPb+ ions was observed as the oxygen jet crossed the plume at high laserfluences, while the signal magnitudes of alI other ions were reduced. This originates from the fact that PbO+ ions dissociate easily to liberate Pb+ ions inthe plume since the bond energy of PbO+ is as low as 2.2 eV.

• Journal of Environmental Science International
• /
• v.11 no.7
• /
• pp.729-735
• /
• 2002

In order to examine the inhibition effect of other heavy metal ions on the removal of heavy metal ions by crab shell in aqueous solution, 10 heavy metal ions $(Cr^{3+},\;Cd^{2+},\;Ni^{2+},\;Zn^{2+},\;Hg^{2+},\;Cu^{2+},\;Mn^{2+],\;Fe^{2+},\;Fe^{3+},\;Pb^{2+})$ were used as single heavy metal ions and mixed heavy metal ions, respectively. In single heavy metal ions, $Pb^{2+},\;Cr^{3+},\;Cu^{2+}$ were well removed by crab shell, however, $Cd^{2+},\;Ni^{2+},\;Zn^{2+},\;Mn^{2+}$ were not. The heavy metal removal increased as the increase of covalent index (Xm$^2$r), and the relationship classified heavy metal ions as 2 heavy metal groups $(Fe^{3+},\;Fe^{2+},\;Cu^{2+},\; Cr^{3+},\;Mn^{2+},\;Ni^{2+},\;Zn^{2+}\;group\;and\;Pb^{2+},\;Hg^{2+},\;Cd^{2+}\;group)$. In mixed heavy metal ions, the removals of $Fe^{2+},\;Fe^{3+},\;Pb^{2+},\;Cu^{2+}$ as 0.49 m㏖/g, regardless of the existence of other heavy metal ions, were similar to the result of single heavy metal ions experiment. The removals of $Mn^{2+},\;Cd^{2+},\;Ni^{2+}$ decreased as the existence of other heavy metal ions, however, the removal of $Zn^{2+},\;Cr^{3+},\;Hg^{2+}$ increased.

• Bulletin of the Korean Chemical Society
• /
• v.27 no.5
• /
• pp.679-686
• /
• 2006

The positions of $PbI _2$ molecule synthesized into the molecular-dimensioned cavities of $\mid K_6 (Pb _4I_2)(PbI_2) _{0.67}-(H_2O)_2\mid [Si _{12}Al _{12}O _{48}]$-LTA have been determined. A single crystal of $\mid Pb _6\mid [Si _{12}Al _{12}O _{48}]$-LTA, prepared by the dynamic ion-exchange of $\mid Na _{12}\mid [Si _{12}Al _{12}O _{48}]$-LTA with aqueous 0.05 M $Pb _(NO _3)_2$ and washed with deionized water, was placed in a stream of flowing aqueous 0.05 M KI at 294 K for three days. The resulting crystal structure of the product $( \mid K_6 (Pb _4I_2)(PbI_2) _{0.67}(H_2O)_2\mid [Si _{12}Al _{12}O _{48}]$-LTA, a = 12.353(1) $\AA$) was determined at 294 K by single-crystal X-ray diffraction in the space group Pm3 m. It was refined with all measured reflections to the final error index $R_1$ = 0.062 for 623 reflections which $F_o$ > 4$\sigma$($F_o$). 4.67 $Pb ^{2+}$ and six $K^+$ ions per unit cell are found at three crystallographically distinct positions: 3.67 $Pb ^{2+}$ and three $K^+$ ions on the 3-fold axes opposite six-rings in the large cavity, three $K^+$ ions off the plane of the eight-rings, and the remaining one $Pb ^{2+}$ ion lies opposite four-ring in the large cavity. 0.67 $Pb ^{2+}$ ions and 1.34 $I^-$ ions per unit cell are found in the sodalite units, indicating the formation of a $PbI _2$ molecule in 67% of the sodalite units. Each $PbI _2$ (Pb-I = 3.392(7) $\AA$) is held in place by the coordination of its one $Pb ^{2+}$ ion to the zeolite framework (a $Pb ^{2+}$ cation is 0.74 $\AA$ from a six-ring oxygens) and by the coordination of its two $I^-$ ions to $K^+$ ions through six-rings (I-K = 3.63(4) $\AA$). Two additional $I^-$ ions per unit cell are found opposite a four-ring in the large cavity and form $Pb _2K_2I^{5+}$ and $Pb _2K_2I^{3+}$ moieties, respectively, and two water molecules per unit cell are also found on the 3-fold axes in the large cavity.

• 한국생물공학회:학술대회논문집
• /
• 2001.11a
• /
• pp.497-500
• /
• 2001

Adsorption characteristics on the biomass of Chlorella sp. HA -1 were investigated in binary system with $Pb^2$, $Cu^2$, $Cd^2$, and $Zn^2$ ions. For the adsorption tests of single metal, Langmuir model was showed good correlation for equilibrium data compared to Freundlich model. Maximum metal uptakes increased as follows: $Pb^2$>$Cd^2$>$Zn^2$>$Cu^2$, whereas the affinity showed different trends: $Cu^2$>>$Cd^2$>$Zn^2$>$Pb^2$. In binary metal system, $Cu^2$ ions inhibited sharply the adsorption of other metal ions except $Pb^2$ ions because of the high biosorption affinity of $Cu^2$ ions. In the case of $Cu^2$ and $Pb^2$ system, there was no significant inhibition on metal uptakes. The results of metal adsorption in the binary system could be explained well on the basis of Langmuir parameters evaluated.

• Bulletin of the Korean Chemical Society
• /
• v.32 no.2
• /
• pp.463-466
• /
• 2011

In this work, we investigate anodization of Pb in ethylene glycol containing small amount of $NH_4F$, demonstrating that ${\beta}-PbF_2$ particles with octahedral morphology can be prepared by adjusting the applied potential and anodizing time. FE-SEM images and XRD measurements of anodic nanostructures as a function of anodizing time clearly show that PbO is first formed on Pb. Subsequently, a local dissolution of PbO leads to formation of skeleton structure of PbO, releasing $Pb^{2+}$ ions in the electrolyte. The lead ions can be precipitated on the walls or intersection of the skeleton walls when the concentration of lead ions is saturated. The method described in this article shows the feasibility of formation of metal fluoride crystal by anodization of metal in a fluoride containing solution.

• Journal of the Korean Chemical Society
• /
• v.68 no.2
• /
• pp.82-86
• /
• 2024

This paper presents the solid-state synthesis of insoluble Prussian blue (Fe₄[Fe(CN)₆]₃·xH₂O, PB) in a ball mill, utilizing the fundamental components of PB. Solid-state synthesis offers several advantages, such as being solvent-free, quantitative, and easily scalable for industrial production. Traditionally, the solid-state synthesis of PB has been limited to the reaction between iron(II/III) ions and hexacyanoferrate(II/III) complex ions, essentially an extension of the solution-based coprecipitation method to solid-state reaction. Taking a bottom-up approach, a reaction is designed where the reactants consist of the basic building blocks of PB: Fe²⁺ ions and CN^- ions. The reaction, with a molar ratio of Fe²⁺ and CN^- corresponding to 1:2.8, yields PB, while a ratio of 1:6.6 results in a mixture of potassium hexacyanoferrate(II) (K₄Fe(CN)₆), potassium chloride (KCl), and potassium cyanide (KCN). This synthetic approach holds promise for environmentally friendly methods to synthesize multimetallic PB with maximum entropy in nearly quantitative yield.

• Analytical Science and Technology
• /
• v.13 no.3
• /
• pp.368-377
• /
• 2000

Si-immobilized Sargassum horneri was used to study the adsorption characteristics along with maximum adsorption conditions of heavy metal ions, Cd(II) and Ph(II) on the Si-immobilized Sargassum horneri. More amount of Cd(II) and Pb(II) ions on the Si-immobilized Sargassum horneri than Sargassum horneri were adsorbed. And Pb(II) ions were more adsorbed in all algae than Cd(II) ions more effectively in alkaline than in acidity. Recovery ratios of Cd(II) and Pb(II) ions on the Sargassum horneri were 58.0-62.6%, 61.2-64.4% respectively, Si-immobilized Sargassum horneri 56.8-92.7%, 37.8-47.9%. Recovery ratio of Cd(II) ion was higher on the Si-immobilized Sargassum horneri but it of Pb(II) ion was lower on the Si-immobilized Sargassum horneri.

• Journal of Environmental Science International
• /
• v.9 no.4
• /
• pp.325-330
• /
• 2000

The hydroxyapatite (HAp) for the present study was prepared by precipitation method in semiconductor fabrication and the crystallized at ambient to 95$0^{\circ}C$ for 30min in electric furnace. The ion-exchange characteristics of HAp for various heavy metal ions such as $Cd^{2+}, Cu^{2+}, Mn^{2+}, Zn^{2+}, Fe^{2+}, Pb^{2+}, Al^{3+}, and Cr^{6+}$ in aqueous solution has been investigated. The removal ratio of various metal ions for HAp were investigated with regard to reaction time, concentration of standard solution, amount of HAp and pH of solution. The order of the ions exchanged amount was as follws: $Pb^{2+}, Fe^{3+}>Cu^{2+}>Zn^{2+}>Al^{3+}>Cd^{2+}>Mn^{2+}>Cr^{6+}. The Pb^{2+}$ ion was readily removed by the Hap, even in the strongly acidic region. The maximum amount of the ion-exchange equilibrium for $Pb^{2+}$ ion was about 45 mg/gram of HAp. The HAp would seem to be possible agent for the removal of heavy metal ions in waste water by recycling of waste sludge in semiconductor fabrication.

• Journal of environmental and Sanitary engineering
• /
• v.12 no.1
• /
• pp.97-100
• /
• 1997

The adsorption of the Chchory particles on Cu(II), Pb(II) and Cd(II) ions were examined by measurements of the adsorption percentage under various condition of temperature, pH, times, heavy metal concentration. Each of 100ml sample solution of Cu(II), Pb(II) and Cd(II) ions mixed with 2g of the Cichory under stirring in shaking water bath for minutes. The solutions were then filtered and pretreatmented according to water pollution official test methods. The concentrations of Cu(II), Pb(II) and Cd(II) ions in the solution were determined by the atomic adsorption spectrophotometer. As a results, the most effective pH of the adsorption of Cu(II), Pb(II) and Cd(II) was 9. With increasing the concentration of heavy metals the amount of adsorption on Cichory was increased. The adsorption equilibrium of Pb(II) and Cd(II) ions were reached to equilibrium by shaking for about 40 minutes. The absorptivities were 85%, 75% respectively.

• Journal of the Korean Ceramic Society
• /
• v.28 no.5
• /
• pp.359-364
• /
• 1991

The effects of Pb5Ge3O11 on the sinterbility and lattice variation of the semiconducting 0.15 mol% Y2O3 doped BaTiO3 have been investigated as functions of additive contents (from 0.25 mol% to 2.5 mol%) and sintering temperatures (from 110$0^{\circ}C$ to 130$0^{\circ}C$). As the amount of Pb5Ge3O11 increases, the sinterbility of BaTiO3 increases abruptly at around 115$0^{\circ}C$. During the sintering, the most of Pb+2 ions in additives penetrate into BaTiO3 lattices and Ge+4 ions present at grain boundaries. Therefore the c lattice of the BaTiO3 increases largely and then the tetragonality increases due to the diffusion of the Pb+2 ions.