• Journal of Korean Society of Environmental Engineers
• /
• v.38 no.4
• /
• pp.169-176
• /
• 2016

This research explored the feasibility of preparing and utilizing preformed polymeric solution of Fe(III) as coagulants for water treatment. The differentiation and quantification of hydrolytic Fe(III) species in coagulant was done by utilizing spectrophotometric method based on the interaction of Fe(III) with Ferron as a complexing agent. The properties of the synthesized polymeric iron chloride (PICl) showed that the quantity of polymeric Fe(III) produced at r = 1.5 was 20% of the total iron in solution, as showing maximum contents. Coagulation experiments were conducted under the condition of various coagulant doses and pH for each coagulant prepared. From the comparison of the characterization of coagulation for $FeCl_3$ (r = 0.0) and PICl (r = 0.5, 1.0, 1.5) coagulants, PICl (r = 0.5, 1.0, 1.5) coagulants was found to be more effective than other coagulant for the removal of organic matters. The experimental results for the coagulation tests at various pH ranges showed that the PICl was least affected by the coagulation pH and PICl was very effective for the removal of turbidity and organic materials over wide pH range (pH 4-9) tested.

• Korean Journal of Environmental Agriculture
• /
• v.13 no.1
• /
• pp.90-97
• /
• 1994

This experiment was conducted to improve the analytical method of tricyclazole- and IBP-combined dust. When the tricyclazole and IBP active ingadients were analyzed by the official analytical method, their recovery rates were 89.5 and 100%, respectively. A reason of the lower recovery rate in tricyclazole was found to be due to strong binding to the minor inorganic compoments, $Al_2O_3$, $Fe_2O_3$, CaO and MgO, of talc and kaoline. However, addition of 0.2% dimethylamine to extraction solvent for tricyclazole- and IBP-combined dust effectively raised the recovery rate of tricyclazole by providing higher basicity than tricyclazole. We have suggest an improved analytical method which is applicable to effective and simultaneous analysis of the active ingradients of tricyclazole- and IBP-combined dust.

• Applied Chemistry for Engineering
• /
• v.20 no.6
• /
• pp.658-662
• /
• 2009

In this work, the amine-treated activated carbon nanotubes (A-MWNTs) were used to investigate the $CO_2$ adsorption behaviors. A-MWNTs were prepared by impregnation with amine in methanol after chemical activation methods using a KOH. The characteristics of amine-treated A-MWNTs were studied by X-ray photoelectron spectroscopy (XPS), $N_2$ adsorption, desorption isotherms at 77 K. The specific surface area and pore volume of the A-MWNTs were analyzed by BET equation, BJH method, and t-plot method. $CO_2$ capture capacity as a function of temperature was measured by temperature programmed desorption (TPD). From the results, the amine treatment increased the basicity and nitrogen content of the A-MWNTs. The $CO_2$ adsorption capacity of the amine-nontreated A-MWNTs showed the highest value at room temperature and then greatly decreased with increasing the temperature. However, the amine-treated A-MWNTs presented a softer slope with temperature compared to the amine-nontreated ones. It was due to the strong interactions between $CO_2$ and amino groups presented on the carbon surfaces studied.

• Journal of Korea Technical Association of The Pulp and Paper Industry
• /
• v.40 no.3
• /
• pp.36-41
• /
• 2008

It is known that ethanolamines play a critical role for deacidification of paper sized by alum-rosin. However, amines also are effective as a chelating agent of metal. The present work was focused on whether amines could scavenge metals and prevent from the aging of paper. Metals such as alum, copper(II) and iron(III) was added to paper, and the paper treated with amines was aged in a thermo-hygrostat for 3-6 days. In the case of paper added to alum, the amines efficiency against paper aging was good in the oder of triethanolamine, diethanolamine and monoethanolamine attributable to the intensity of basicity and steric effect. Even in the case of paper treated with copper(II) chloride, iron(III) chloride, and copper(II) chloride, the significant preservation efficiency was shown by ethanolamine during accelerated aging. This outcome pinpoints the fact that ethanolamine can prevent paper aging not only from acid by neutralizing acid contained in paper but also from metals by producing of complexes with metals. These consequences above convince that ethanolamine makes it possible for mass deacidification for paper which contains acid and metals. Future studies should be conducted concerning whether, in reality, the treatment of its gas mode, in a single or multiple applications, has significant effect on lessening paper aging.

• Applied Chemistry for Engineering
• /
• v.21 no.3
• /
• pp.278-283
• /
• 2010

The cationic polymerization of oxolane high explosives which have pendant explosive groups such as azido, nitrato and hydrazino is investigated theoretically using the semiempirical MINDO/3, MNDO and AM1 methods. The nucleophilicity and basicity of oxolane high explosives can be explained by the negative charge on oxygen atom of oxolane. The reactivity of propagation in the polymerization of oxolane can be represented by the positive charge on carbon atom and the low LUMO energy of active species of oxolane. The reaction of the oxolane high explosives in oxonium ion form to the open chain carbenium ion form is expected by computational stability energy (17.950~30.197 kcal/mol) of the oxonium ion and carbenium ion favoring the carbenium ion. The relative equilibrium concentration of cyclic oxonium ion and carbenium ion is found to be a major determinant of mechanism, owing to the rapid equilibrium of these catoinic forms. Based on calculation, in the prepolymer propagation step, $S_N1$ mechanism will be at least as fast as that for $S_N2$ mechanism.

• Applied Chemistry for Engineering
• /
• v.16 no.4
• /
• pp.588-593
• /
• 2005

In this study, biodegradable poly(${\varepsilon}$-caprolactone) (PCL) microcapsules containing chemically treated $SiO_2$ and nifedipine were prepared by oil-in-water (O/W) emulsion solvent evaporation method. The microcapsules containing drugs were confirmed using FT-IR spectra. The morphologies of the microcapsules were observed with scanning electron microscope (SEM). The nifedipine's release behaviors from the microcapsules were also examined with UV/vis spectroscopy. As a result, the inclusion of nifedipine into the microcapsules was determined by the presence of nifedipine's specific peak, i.e., C=O stretch vibration at $1682cm^{-1}$. The average particle size of the microcapsules decreased with increasing stirring rate. The nifedipine adsorption capacity and release rate of treated $SiO_2$ that was treated with basic solution decreased because with the increased basicity it lowered the specific surface area of $SiO_2$ and promoted stronger acid-base interactions between $SiO_2$ and nifedipine.

• Journal of the Korean Chemical Society
• /
• v.36 no.2
• /
• pp.197-204
• /
• 1992

The cationic polymerization of cyclic acetals are investigated theoretically using the semiempirical MINDO/3, MNDO, and $AM_1$, methods. The nucleophilicity and basicity of cyclic acetals can be explained by the negative charge on oxygen atom of cyclic acetals. The reactivity of propagation in the polymerization of cyclic acetals can be represented by the positive charge on $C_2$ atom and the low LUMO energy of active species of cyclic acetals. The reactivity of 2-buthyl-1,3-dioxepane(2-Bu-DOP) of cyclic oxonium and opening carbenium ion form is expected computational stability of the oxonium ion by 5${\sim}$7kcal/mole favoring the carbenium ion. Owing to the rapid equilibrium of these cation forms and the reaction coordinate based on calculation that the reaction coordinate based on calculation that the chain growth $S_N1$ mechanism will be at least as fast as that for $S_N2$ mechanism.

• Bulletin of the Korean Chemical Society
• /
• v.29 no.7
• /
• pp.1359-1363
• /
• 2008

Second-order rate constants have been determined spectrophotometrically for reactions of 2,4-dinitrophenyl 2- thiophenecarboxylate (2) with a series of alicyclic secondary amines in 80 mol % $H_2O$/20 mol % DMSO at 25.0 ${\pm}$ 0.1 ${^{\circ}C}$. The Brønsted-type plot exhibits a downward curvature, i.e., the slope decreases from 0.74 to 0.34 as the amine basicity increases. The $pK_a$ at the center of the Brønsted curvature, defined as $pK_a^o$, has been determined to be 9.1. Comparison of the Brønsted-type plot for the reactions of 2 with that for the corresponding reactions of 2,4-dinitrophenyl 2-furoate (1) suggests that reactions of 1 and 2 proceed through a common mechanism, although 2 is less reactive than 1. The curved Brønsted-type plot has been interpreted as a change in RDS of a stepwise mechanism. The replacement of the O atom in the furoyl ring by an S atom (1 $\rightarrow$ 2) does not alter the reaction mechanism but causes a decrease in reactivity. Dissection of the apparent second-order rate constants into the microscopic rate constants has revealed that the $k_2/k_{-1}$ ratio is not influenced upon changing the nonleaving group from furoyl to thiophenecarbonyl. However, $k_1$ has been calculated to be smaller for the reactions of 2 than for the corresponding reactions of 1, indicating that the C=O bond in the thiophenecarboxylate 2 is less electrophilic than that in the furoate 1. The smaller k1 for the reactions of 2 is fully responsible for the fact that 2 is less reactive than 1.

• Bulletin of the Korean Chemical Society
• /
• v.34 no.10
• /
• pp.2983-2988
• /
• 2013

Second-order rate constants ($k_N$) have been measured spectrophotometrically for the reactions of 4-chloro-2-nitrophenyl X-substituted-benzoates (1a-1h) with a series of cyclic secondary amines in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$. The Hammett plot for the reactions of 1a-1h with piperidine consists of two intersecting straight lines, while the Yukawa-Tsuno plot exhibits an excellent linear correlation with ${\rho}_X $ = 1.25 and r = 0.58, indicating that the nonlinear Hammett plot is not due to a change in the rate-determining step (RDS) but is caused by ground-state stabilization through resonance interactions for substrates possessing an electron-withdrawing group in the benzoyl moiety. The Br${\o}$nsted-type plot for the reactions of 4-chloro-2-nitrophenyl benzoate (1d) with a series of cyclic secondary amines curves downward with ${\beta}_2$ = 0.85, ${\beta}_1$ = 0.24, and $pK_a{^o}$ = 10.5, implying that a change in RDS occurs from the $k_2$ step to the $k_1$ process as the $pK_a$ of the conjugate acid of the amine exceeds 10.5. Dissection of $k_N$ into the microscopic rate constants $k_1$ and $k_2/k_{-1}$ ratio associated with the reaction of 1d reveals that $k_2$ is dependent on the amine basicity, which is contrary to generally held views.

• Proceedings of the Korea Crystallographic Association Conference
• /
• 2002.11a
• /
• pp.19-19
• /
• 2002

Perovskite-type titanate dielectrics have attracted much attention in memory devices such as DRAMs or FeRAMs due to their high dielectric constants. However, low volatility of the Ba, Sr, Pb or Zr precursors with only thd ligands has limitations in obtaining high quality thin films by liquid source metal organic chemical vapor deposition (LS-MOCVD) processes. To improve the volatility of these precursors, many attempts have been made such as adding polyether ligands to satisfy the coordinative saturation. We report the synthesis of new precursors Ba(thd)₂(tmeea) and Sr(thd)₂(tmeea), where tmeea = tris[2-(2-methoxyethoxy)ethyl]amino, and LS-MOCVD of barium strontium titanate (BSTO) thin films using these precursors. Due to increased basicity of amines compared with ethers, it is expected that the nitrogen-donor ligand will make a strong bond to a metal than an analogous oxygen-donor ligand, consequently improving the volatility and thermal behavior of these precursors. Thin films of BSTO were grown on Pt(111)/SiO₂/Si(100) substrates by LS-MOCVD using a cocktail source consisting of the conventional Ti precursor Ti(thd)₂(O/sup i/Pr), and these new Ba and Sr precursors. As-grown films were characterized by XPS, SEM, XRD, XRF, and C-V and I-V measurements. BSTO films grown at 420℃ were stoichiometric barium strontium titanate with very smooth surface morphology and their dielectric constants were found to be as targe as 450. Dependence of the composition, microstructure and the electrical properties of the BSTO films on the growth temperature, annealing temperature, working pressure, and the composition of the cocktail source will be discussed.