• 한국환경과학회지
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• 제9권4호
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• pp.325-330
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• 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.

• Carbon letters
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• 제4권1호
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• pp.21-23
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• 2003

In this work, the effect of anodic oxidation treatment on Cr(VI) ion adsorption behaviors of activated carbon fibers (ACFs) was investigated. The aqueous solutions of 10 wt% $H_3PO_4$ and $NH_4OH$ were used for acidic and basic electrolytes, respectively. Surface characteristics and textural properties of ACFs were determined by XPS and $N_2$ adsorption at 77 K. The heavy metal adsorption of ACFs was conducted by ICP. As a result, the adsorption amount of the anodized ACFs was improved in order of B-ACFs > A-ACFs > pristine-ACFs. In case of the anodized treated ACFs, the specific surface area was decreased due to the pore blocking or pore destroying by acidic electrolyte. However, the anodic oxidation led to an increase of the Cr(VI) adsorption, which can be attributed to an increase of oxygen-containing functional groups, such as, carboxylic, lactonic, and phenolic groups. It was clearly found that the Cr(VI) adsorption was largely influenced by the surface functional groups, in spite of the reduced specific surface area of the ACFs.

• Bulletin of the Korean Chemical Society
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• 제11권1호
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• pp.54-58
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• 1990

Acid-base equilibria and spectroscopic properties of diazepam and chlorodiazepoxide were investigated in sodium dodecyl sulfate (SDS) micellar solutions as functions of pH. The results were compared with the behaviors in homogeneous aqueous media. The presence of SDS increased the $pK_a$ of chlorodiazepoxide to 6.3 from 4.7, while it has little effect on the $pK_a$ of diazepam. The acidic protonated form of diazepam was moderately fluorescent when the solution was excited at 350 nm, and emissnion intensity of the species was enhanced about 5 fold by the presence of SDS. On the other hand, the acidic solution of chlorodiazepoxide was non-fluorescent, but the neutral solution of the compound was fluorescent upon excitation at 350 nm. The emission peak of the neutral chlorodiazepoxide shifted to shorter wavelength region without significant change in the emission intensity upon the addition of SDS. Procedures for assay of the individual drugs from their mixture by the use of SDS micelle were discussed.

• 분석과학
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• 제22권6호
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• pp.519-523
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• 2009

본 연구는 수용액 중에 존재하는 방사성 동위원소인 요오드 즉, 요오드이온($I^-$), 요오드산이온(${IO_3}^-$)및 요오드($I_2$)를 효과적으로 제거하는 방법에 관한 것이다. 별도로 물리적 화학적 변화의 과정이 필요하지 않고, 표면 개질된 활성 산화알루미늄과 활성탄을 이용하여 완전하게 제거할 수 있어 방사성 폐수 및 일반 산업폐수에도 유용하게 적용될 수 있다. 요오드이온($I^-$), 요오드산이온(${IO_3}^-$)의 혼합수용액 중의 각 이온들을 은 처리된 염기성 알루미나와 산성 알루미나를 이용한 흡착제거 방법으로 각각 99% 이상 제거하는 효과를 나타내었다.

• Tribology and Lubricants
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• 제18권4호
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• pp.299-304
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• 2002

This paper reports the studies on the wear-corrosion behavior of ductile cast iron in the acidic environment. In atmosphere and variety of pH solution, specific wear rate and wear-corrosion characteristics of GCD 60 with various sliding speed and distance were investigated. And electrochemical polarization test of GCD 60 was examined in the environment of various pH values. The main results are as following : As the contact pressure increases, the critical velocity of specific wear rate becomes transient at low sliding speed. As pH value becomes low, wear-corrosion loss increases in the aqueous solution. As the corrosion environment is acidified, corrosion potential of GCD 60 becomes noble and corrosion current density increases.

• 대한화학회지
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• 제28권3호
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• pp.176-184
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• 1984

XAD-2 지지체를 이용하여 알코올성 수용액 중에서 벤조산과 그 유도체들의 머무름 거동을 조사하였으며, 또한 분리를 시도하였다. 벤조산과 그 유도체들의 머무름은 첨가한 유기용매의 농도와 종류, 유동상의 pH와 첨가된 $R_4N^+$에 의해 영향을 받았으며 시료 분자내의 치환기 종류와 위치에 의해서도 영향을 받았다. 약산 분자들이 산성 용액에서는 주로 흡착에 의하여 무극성 XAD-2표면에 머무름이 되고 반대이온을 첨가한 경우 염기성 용액에서는 이온쌍 모델을 따라 약산의 전리된 음이온들이 머무르는 것을 확인하였다. 이러한 결과들을 기초로 pH 8.50의 염기성 수용액에서 혼합시료를 분리하였다.

• Bulletin of the Korean Chemical Society
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• 제23권4호
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• pp.549-554
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• 2002

Thermosensitive poly(organophosphazenes) bearing methoxy-poly(ethylene glycol) (MPEG) and alkylamines as substituents have been synthesized and characterized by elemental analysis, NMR spectroscopy, GPC, and DSC. All the polymers exhibited crystallinity, which was probably induced by the MPEG side chain of the polymers. All the polymers exhibited the lower critical solution temperature (LCSTs) in the range of 28 to $94^{\circ}C$ depending on several factors such as mole ratio of the substituents, kinds of PEG and alkylamines. The higher content of MPEG and shorter chain length of alkylamines of the polymers afforded the higher LCST. The LCSTs of the polymers exhibited almost concentration-independent behavior in the range of 3-30 wt % of the polymers in aqueous solutions. The polymers showed the higher LCSTs in the acidic solutions than in the neutral and basic solutions. The ionic strength of the polymer solution affected the LCST, which decreased with increased NaCl concentration. The polymer bearing almost equimolar substitutuents with the -N-P-N- unit has shown the LCST more sensitive to NaCl and pH than that with the -N-P-O- unit. The polymers were found to degrade in acidic solution but be very stable in alkali solution as well as in the buffer solution of pH 7.4.

• 공업화학
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• 제21권2호
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• pp.188-194
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• 2010

전해살균수는 수도물에 식염이나 염산 등의 전해보조제를 첨가시킨 수용액을 전기분해하여 유용한 기능을 갖게 한 수용액이다. 전해살균수는 살균을 목적으로 한 식품위생관리에 사용되는 것으로, 강산성전해수, 미산성전해수 및 차아염소산나트륨수로 나눌 수 있다. 본 연구에서는 살균효과를 지닌 전해살균수의 제조원리, 장단점 분석과 함께 연도별, 국가별, 출원인별, 기술종류별로 기술동향 특허분석을 하였다.

• Journal of Pharmaceutical Investigation
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• 제30권4호
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• pp.267-271
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• 2000

The effect of cyclodextrins on the solubility and stability of aspalatone (acetylsalicylic acid maltol ester, AM, CAS 147249-33-0), which has been recently found to have an antithrombotic effect, was investigated. The addition of ${\beta}-cyclodextrin\;({\beta}-CD),\;dimethyl-{\beta}-cyclodextrin\;(DMCD)\;or\;2-hydroxypropyl-{\beta}-cyclodextrin\;(HPCD)$ to the aqueous solution increased the solubility of AM concentration-dependently. From the phase solubility diagram, stability constants for $AM-{\beta}-CD$, -DMCD or -HPCD complexes were calculated to be 43.1, 78.3 and $53.0\;M^{-1}$. The addition of ${\beta}-CD$, DMCD or HPCD to AM solution retarded the degradation rate of AM in the acidic region. However, ${\beta}-CD$ and HPCD rather acted as an accelerator of degradation in the neutral and alkaline regions. DMCD had a stabilizing effect at all pHs studied.

• Bulletin of the Korean Chemical Society
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• 제19권2호
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• pp.197-201
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• 1998

The complex formation from Cu(Ⅱ) ion and 1,3-bis(tris(hydroxymethyl)methylamino)propane (bistrispropane) in aqueous solution has been studied potentiometrically and spectrophotometrically. Bistrispropane (btp) coordinates to Cu(Ⅱ) as multidentate. In the btp (L) complex CuL2+, two of the hydroxyl oxygen atoms as well as the amine nitrogens of the ligand are coordinated. In neutral and weakly acidic media, one of the coordinated hydroxyl groups is deprotonated. In basic media, an additional hydroxyl group undergoes deprotonation. The equilibrium constants for the formation of CuL2+, CuLH-1+, and CuLH-2 have been determined. The nature of the coordinate bonds has been deduced from the potentiometric data and the spectra of these complexes.