• 공업화학
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• 제10권6호
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• pp.857-862
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• 1999

아민화된 poly(ether sulfone)(APES)는 poly(ether sulfone)(PES)를 질산과 황산(촉매)의 혼산으로 니트로화한 poly(ether sulfone)(NPES)를 아민화하여 제조되었다. FT-IR의 분석 결과 1537과 $1351cm^{-1}$에서 $NO_2$의 비대칭 신축진동과 대칭 신축진동에 의한 흡수피크로 니트로화가 되었음이 확인되었다. 또한 NPES의 아민화는 $NO_2$에 의한 흡수피크가 사라지고 3470과 $3374cm^{-1}$에서 $NH_2$기에 의한 비대칭 신축진동과 대칭 신축진동의 흡수피크로 확인되었다. PES(5 g; 21.55 mmol.)에 대한 니트로화의 최적 조건은 반응시간 12시간, 반응온도 $120^{\circ}C$, 질산의 농도 28.00 mmol. 황산의 농도 52.00 mmol. 이었다. APES의 원소분석결과 반복단위당 0.89개의 아민기가 도입되었다. 실리카겔이나 활성탄소보다 흡착속도는 느리나 NO에 대한 흡착능이 우수하였고, 화학적인 흡착속도는 물리적 흡착속도보다 느리며, 화학적 흡착량이 물리적 흡착량 보다 높은 것을 알 수 있었다.

• 멤브레인
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• 제28권5호
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• pp.326-331
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• 2018

축전식 탈염(capacitive deionization)에 이용할 수 있는 폴리페닐렌 옥사이드(PPO) 음이온 교환막의 가교결합에 대해 조사하였다. 브롬화와 아민화 반응단계를 거쳐 PPO 음이온 교환 고분자를 제조하고 비스페놀 A 디글리시딜에테르(BADGE), m-페닐렌디아민(m-PDA), 헥사메틸렌디아민(HMDA) 등으로 가교하였다. 가교에 따른 겔화되는 시간은 HMDA > m-PDA > BADGE 순으로 짧았으며, 일정한 함량 이상으로 실온에서 가교하면 1-메틸피롤리돈(NMP)과 같은 비양성자성 용매(aprotic solvent)에 녹지 않아 내화학성이 증대되었다. 가교제(BADGE) 함량에 따른 음이온 교환막의 이온 교환 용량과 함수율을 측정하고 비교하였다. HMDA 용액에 침적하여 표면 가교한 PPO 음이온 교환막을 축전식 탈염에 적용한 결과 그 탈염 성능은 가교하지 않은 막과 비교하여 흡착단계의 초기 부분을 제외하고 거의 차이가 없었다.

• 한국토양환경학회지
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• 제2권2호
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• pp.25-33
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• 1997

비점오염원으로 토양과 수환경에 영향을 미치는 우분퇴비의 영향을 조사하기 위하여 상부와 하부에 연결한 다층토양칼럼을 가지고 음이온의 토양으로부터 용출경향을 조사하였다. 상부 칼럼은 건조 우분 퇴비를 0, 2,4, 6%의 비율로 Ap토양에 처리한후 균일하게 채웠고 하부칼럼은 15, 30, 45cm의 길이의 아크릴칼럼에 B층 토양을 용적비중 1.3g/$\textrm{cm}^3$으로 채운 후 결합하였다. 이렇게 조합된 칼럼을 충분히 포화시킨 후 증류수를 칼럼의 상부에서 일정 수두높이를 유지하면서 칼럼의 하부에서 수집되는 용출수의 수리전도도와 용출된 음이온의 농도를 조사하였다. 상부와 하부의 각각의 수리전도도는 3$\times$$10^{-4}$cm/sec 와 1.6$\times$$10^{-3}$cm/sec 이었고 비특정흡착특성을 지니는 대부분의 수용성 염소와 황산이온은 90%가 0.2 공극수량에서 그리고 대부분의 음이온은 1 공극수량이내에 용출되는 경향을 보였는데 이는 이들 이온이 토양에 가해진 유기물에 의해 이동에 영향을 받지 않았음을 보여주는 것이다. 또한 이들 음이온이 통과하는 토양의 깊이도 이들 음이온의 이동에 영향을 주지 않았음을 알 수 있었다. 그러나 비특정과 특정 모두의 흡착특성을 가지는 황산이온의 경우 용출곡선이 오른쪽으로 약간 이동하여 용출이 지연되는 경향을 보여주고 있다. 그리고 인산이온의 경우 조사된 5 공극수량 이내에서 전혀 용출되지 않았다.

• Membrane and Water Treatment
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• 제11권1호
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• pp.69-77
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• 2020

Former studies revealed that sepiolite thermally treated at high temperature have high adsorption capacity for phosphate. However, its micron size (75 ㎛) limits its application to water treatment. In this study, we synthesized sepiolite impregnated polysulfone (PSf) beads to separate it easily from an aqueous solution. PSf beads with different sepiolite ratios were synthesized and their efficiencies were compared. The PSf beads with 30% impregnated sepiolite (30SPL-PSf bead) possessed the optimum sepiolite ratio for phosphate removal. Kinetic, equilibrium, and thermodynamic adsorption experiments were performed using the 30SPL-PSf bead. Equilibrium adsorption was achieved in 24 h, and the pseudo-first-order model was suitable for describing the phosphate adsorption at different reaction times. The Langmuir model was appropriate for describing the phosphate adsorption onto the 30SPL-PSf bead, and the maximum adsorption capacity of the 30SPL-PSf bead obtained from the model was 24.48 mg-PO₄/g. Enthalpy and entropy increased during the phosphate adsorption onto the 30SPL-PSf bead, and Gibb's free energy at 35 ℃ was negative. An increase in the solution pH from 3 to 11 induced a decrease in the phosphate adsorption amount from 27.30 mg-PO₄/g to 21.54 mg-PO₄/g. The competitive anion influenced the phosphate adsorption onto the 30SPL-PSf bead was in the order of NO₃^- > SO₄^2- > HCO_3^-. The phosphate breakthrough from the column packed with the 30SPL-PSf bead began after ~2000 min, reaching the influent concentration after ~8000 min. The adsorption amounts per unit mass of 30SPL-PSf and removal efficiency were 0.775 mg-PO₄/g and 61.6%, respectively. This study demonstrates the adequate performance of 30SPL-PSf beads as a filter for phosphate removal from aqueous solutions.

• Bulletin of the Korean Chemical Society
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• 제27권4호
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• pp.545-548
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• 2006

We investigated the Surface-enhanced Raman Spectroscopy (SERS) spectrum of ethephone (2-chloroethylphosphonic acid). We observed significant signals in the ordinary Raman spectrum for solid-state ethephone as well as when it was adsorbed on a colloidal silver surface, strong vibrational signals were obtained at a very low concentration. The SERS spectra were obtained by silver colloids that were prepared by the $\gamma$-irradiation method. The influence of pH and the influence of anion $(Cl^-,\;Br^-,\;I^-)$ on the adsorption orientation were investigated. Two different adsorption mechanisms were deduced, depending on the experimental conditions. The chlorine atom or the chlorine and two oxygen atoms were adsorbed on the colloidal silver surface. Among halide ions, $Br^-$ and $I^-$ were more strongly adsorbed on the colloidal silver surfaces. As a result, the adsorption of ethephone was less effective due to their steric hinderance.

• 한국환경과학회지
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• 제16권6호
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• pp.689-698
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• 2007

Mesoporous silicas for heavy metals adsorption were prepared by co-condensation of surfactant as a template and Ludox HS-40 as a silica precursor. Various mesoporous silicas with the introduction of chelating ligands (mercaptopropyl and aminopropyl groups) were synthesized to remove heavy metal ions from aqueous solutions. The surface modification was conducted with a co-condensation process using the sequential or simultaneous addition of mesoporous silica and high concentration of the organosilane(3-mercaptopropyltrimethoxysilane and 3-aminopropyltriethoxysilane). These materials have been characterized by elemental analysis, XRD, SEM and TEM analysis. Adsorbents synthesized with 3-mercaptopropyltrimethoxysilane and 3-aminopropyltriethoxysilane shows a high loading capacity for Hg(II), Pb(II), Cd(II) and anion Cr(VI). Especially the one synthesized with a mercaptopropyl function has the highest adsorption capacity for Hg(II) and Cd(II).

• 한국입자에어로졸학회지
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• 제9권4호
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• pp.221-230
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• 2013

We demonstrated the efficacy of magnetic nanoparticles (MNPs) produced from a low grade iron ore as an adsorbent for the removal of Cr(VI), a toxic heavy metal anion present in wastewater. The adsorption of Cr(VI) by these MNPs strongly depended on the dosage of MNPs, the initial concentration of the Cr(VI) solutions, and pH. The highest Cr(VI) adsorption efficiency of 22.0 mg/g was observed at pH 2.5. The adsorption data were best fit with the Langmuir isotherm and corresponded to a pseudo-second-order kinetic model. The used adsorbent was regenerated by eluting in highly alkaline solutions. Sodium bicarbonate showed the highest desorption efficiency of 83.1% among various eluents including NaOH, $Na_2HPO_4$, and $Na_2CO_3$. Due to the high adsorption capacity, the simple magnetic separation, and the high desorption efficiency, this nano-adsorbent produced from inexpensive and abundant resources may attract the attention of the industries to apply for removing various metal anionic contaminants from wastewater.

• 한국물환경학회지
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• 제23권1호
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• pp.27-32
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• 2007

This study focused on estimating the feasibility of a strong basic anion exchanger (PA312OH) as a sorbent for the removal of residual reactive dye and saving chemicals and water. Cellulose reactive dye C.I.RB49 was tested because reactive dye is the largest single group of dyes and that dye needs larger amount of inorganic salts as dyeing agent but nearly 50% of reactive dyes may be lost to the effluent. The adsorption characteristics of PA312OH for C.I.RB49 were as follows. Ion-selectivity among the dye and inorganic salts was Dye > ${SO_4}^{2-}$ > ${CO_3}^{2-}$ > $Cl^-$. C.I.RB49 was exchanged more than 3 times ${SO_4}^{2-}$ and ${CO_3}^{2-}$ and $Cl^-$ was not exchanged absolutely. The exchanging velocity was increased exponentially with increasing temperature. This result is positive effect on treating the high temperature dyeing process wastewater. The exchanged dye percents to initial were 96.8% and 99% at flow rate 20.5 mL/min. and 3.7 mL/min.. The exchanging capacity of PA312OH for C.I.RB49 was 215.2 mg/g at conc.=369.2 mg/L, Temp.=$25^{\circ}C$. 74% inorganic salts were recrystallized from real dark reactive color dyeing wastewater treated with PA312OH.

• 공업화학
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• 제18권5호
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• pp.454-458
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• 2007

본 연구는 알루미나를 이용하여 수용액 중에 존재하는 $Ca^{2+}$, $Mg^{2+}$, $Sr^{2+}$, $SO{_4}^{2-}$, $NO{_3}^-$, $Cl^-$ 이온의 제거 특성을 분석하기 위하여 실시하였다. 알루미나는 $Al(NO_3)_3{\cdot}9H_2O$와 $NH_4OH$를 사용하여 합성한 수화물을 $450{\sim}750^{\circ}C$로 5 h 동안 열처리하고 FT-IR과 Brunauer-Emmett-Teller (BET)법으로 물성을 분석하였다. 실험결과에 의하면 알루미나의 비표면적은 열처리 온도가 증가하면 감소하는 특성을 나타내었다. 알루미나에 의한 흡착능은 $SO{_4}^{2-}$와 $NO{_3}^-$가 각각 23 mg/g와 12.4 mg/g의 값을 보였다. 반면에 $Cl^-$는 4 mg/g으로 비교적 낮은 값을 보였다. 일반적으로 음이온 제거 효율은 알루미나의 제조를 위한 열처리 온도가 증가할수록 감소하였으며, $450^{\circ}C$로 처리한 알루미나의 경우에 가장 좋은 처리 효율을 나타내었다. 양이온인 $Ca^{2+}$, $Mg^{2+}$, $Sr^{2+}$의 제거 효율은 알루미나의 열처리 온도에 비례하여 증가하는 경향을 보였다.

• Journal of Microbiology and Biotechnology
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• 제19권4호
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• pp.416-423
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• 2009

Hepatitis B core antigen(HBcAg) is an important serological marker used in the diagnosis of hepatitis B virus(HBV) infections. In the current study, a fast and efficient preparative purification protocol for truncated HBcAg from Escherichia coli disruptate was developed. The recombinant HBcAg was first captured by anion exchange expanded bed adsorption chromatography integrated with a cell disruption process. This online capture process has shortened the process time and eliminated the "hold-up" period that may be detrimental to the quality of target protein. The eluted product from the expanded bed adsorption chromatography was subsequently purified using size-exclusion chromatography. The results showed that this novel purification protocol achieved a recovery yield of 45.1% with a product purity of 88.2%, which corresponds to a purification factor of 4.5. The recovered HBcAg is still biologically active as shown by ELISA test.