• Proceedings of the Materials Research Society of Korea Conference
• /
• 2003.03a
• /
• pp.248-248
• /
• 2003

층상이중수화물(Layered Double Hydroxides, LDH)은 층 사이에 무기물 음이온이 있는 2차원 충상구조물로서 이들 층 사이의 공간에 이동 가능한 수화된 음이온의 존재로 전하균형을 이룬다. 층 사이의 음이온은 교환이 가능하며, 나머지의 공간은 물분자로 채워져 있다. 이러한 특성을 응용하여 LDH는 촉매, 음이온 교환제, 흡착제, 담체로 사용가능하며, 특히 음이온 교환능이 있는 소재로 고분자에 적용되고 있으며, 층간에 염료를 삽입한 복합체의 제조 둥에 관한 연구가 활발히 이루어지고 있다. 이의 적용에서 LDH의 입도는 결정적인 한계 요인으로 작용하기도 한다. 본 실험에서는 Mg-Al-NO$_3$ 층상이중수산화물(Mg-Al-NO$_3$-LDH)을 공침전법으로 합성하고, 양이온의 농도와 공침시 pH 및 교반조건의 변화가 생성된 LDH의 결정상, 형상, 입도, 및 양이온교환능에 미치는 영향을 알아보았다. 특히 초음파 분산법을 적용하는 경우 생성되는 LDH 입자크기의 미세화에 효과적인 것을 확인 할 수 있었다.

• Proceedings of the Korean Environmental Sciences Society Conference
• /
• 2006.05a
• /
• pp.278-279
• /
• 2006

본 연구에서는 수중 silica 제거에 이온교환수지의 성능이 실험되었다. 음이온 단일수지에 비해 양이온/음이온 혼합수지가 silica제거에 효과적이었고, 혼합수지에서 온도가 높을수록 교환반응속도는 빨랐다. 음이온과 양이온교환능은 용액의 pH를 변화를 측정하여 해석할 수 있었다. 용액에 공존하는 양이온인 $Na^+$는 혼합수지에서 pH변화에 영향을 주는 물질이었고, 이러한 pH의 변화는 silica의 제거능에 영향을 주었다. 각 온도에서 도달된 평형농도로부터 각 수지에 대한 silica의 선택도계수가 측정되었다.

• Korean Chemical Engineering Research
• /
• v.46 no.2
• /
• pp.436-442
• /
• 2008

Organic-inorganic hybrid mesoporous anion-exchange resins were prepared for the adsorption of anions from aqueous solutions. The prepared samples were characterized using nitrogen adsorption-desorption measurements, Fourier transform infrared (FTIR) spectroscopy, and elemental analyses. Batch and kinetic experiments were performed to examine the anion-exchange performances of the prepared samples. Among the prepared samples, the hybrid mesoporous anion-exchange resins functionalized with tributylammonium groups showed higher adsorption capacities for perrhenate ions than did the resin functionalized with trimethylammonium groups. The surfactant, hexadecylamine, which had hydrophobic alkyl chains, also showed affinity for hydrophobic perrhenate anions.

• Applied Chemistry for Engineering
• /
• v.10 no.2
• /
• pp.206-211
• /
• 1999

Mixed-bed ion exchange performance was studied experimentally with variations of cation to anion resin ratio, resin weight and temperature at ultralow sodium chloride solution concentrations of less than $1.0{\times}10^{-4}M$. Analyzing the effluent concentration histories the performance test was examined as a function of tested solution volume for a laboratory-scale continuous flow column until both the cation and anion-exchange resins were exhausted. Initial leakage was observed for both cation and anion breakthrough curves, but serious at cation breakthrough curve because of low selectivity coefficient. The slope of breakthrough curve was affected by selectivity coefficient and temperature. The slope of anion breakthrough curve was steep because of the large selectivity coefficient, and ion exchange rates increased as temperature increased. The temperature effect decreased as the total volume was increased or as the resins were exhausted.

• Journal of Korean Society of Environmental Engineers
• /
• v.28 no.5
• /
• pp.527-534
• /
• 2006

The purpose of this study is the development of more effective filter-type polymer adsorbent for removal of anionic pollutants from wastewater. In order to synthesize the polymer adsorbent that possesses anionic exchangeable function, carboxyl(-COOH) group of PP-g-AA nonwoven fabric was converted into amine($-NH_2$) group by the chemical modification using diethylene triamine(DETA). FT-IR data indicate that amine group was introduced into PP-g-AA through amidation of grafted acrylic acid by reaction with DETA. The degree of amination increased with increase in the reaction time and temperature of the chemical modification process, and was significantly improved by the pre-swelling treatment of PP-g-AA with solvent and addition of metal chlorides as a catalyst in following order as $NH_4OH>MeOH{\geq}HCl{\geq}H_2O\;and\;AlCl_3>FeCl_3{\geq}SnCl_2{\gg}ZnCl_2{\geq}FeCl_2$, respectively. However, the addition of catalyst limited the reusability of DETA, hence was less useful from the viewpoint of cost effectiveness and waste management. The anion exchange capacity of the aminated PP-g-AA(PP-g-AA-Am) increased with increase in the degree of amination, but it reached maximum value at the degree of amination as about $50{\sim}60%$. The anion exchange capacity of PP-g-AA-Am was higher than those of commercial anion resins.

• Polymer(Korea)
• /
• v.25 no.3
• /
• pp.311-317
• /
• 2001

In this study, we synthesized bead-type GMA-DVB copolymer using glycidylmethacrylate (GMA) with high reactivity and hydrophilicity. Macrorecticular anion exchanger containing the trimethylammonium group were then prepared by amination with trimethylammonium chloride. We observed that the size of $NO_3^-$ is smaller than that of $SO_4^{2-}$ which disturb $NO_3^-$ removal in most of coexistent anions in ground water. Thus we investigated selective affinity for $NO_3^-$ and properties of individual ion exchangers with various DVB content. For each resins, we confirmed formation of copolymer by FT-IR spectrometer and investigated ion exchange capacity, swelling ratio, the amination yield and the effect with degree of crosslinking on adsorbability for nitrate. When amount of DVB is 4 wt%, amination yield, ion exchange capacity and swelling ratio was 384.3%, 3.25 meq/g and 77.1%, respectively. In these result, it can found that synthetic optimal condition is 4 wt% DVB content for monomer.

• Journal of Korean Society of Environmental Engineers
• /
• v.31 no.9
• /
• pp.775-782
• /
• 2009

PP-g-AA-Am nonwoven fabric, which possess anionic exchangeable function, was prepared by chemical modification of carboxyl (-COOH) group of PP-g-AA nonwoven fabric to amine ($-NH_2$) group using diethylene triamine (DETA). Its adsorption characteristics for anionic nutrients including isotherm, kinetics and co-anions were studied by batch adsorption experiments. Adsorption equilibriums of $PO_4$-P on PP-g-AA-Am fabric were well described by the Langmuir isotherm model, and their adsorption energies were ranged 10.3 kJ/mol indicating an ion-exchange process as primary adsorption mechanism. The adsorption selectivity of PP-g-AA-Am nonwoven fabric for anions under competition with each other was in following order: $SO_4\;^{2-}$>$PO_4\;^{3-}$>$NO_3\;^-$>$NO_2\;^-$. Also, all results obtained from this study indicate that the $PO_4$-P removal capacity of PP-g-AA-Am nonwoven fabric was extremely superior to that of PA308 anion-exchange resin.

• Membrane Journal
• /
• v.32 no.5
• /
• pp.348-356
• /
• 2022

With the development of the bio industry, membrane chromatography with a high adsorption efficiency is emerging to replace the existing column chromatography used in the downstream processes of pharmaceuticals, food, etc. In this study, through the deacetylation reaction of two commercial cellulose acetate (CA) membranes with different pore sizes, the porous regenerated cellulose (RC) supports for membrane chromatography were obtained to attach the anion exchange ligands. The adsorptive membranes for anion exchange were prepared by attaching an anion exchange ligand ([3-(methacryloylamino) propyl] trimethylammonium chloride) containing quaternary ammonium groups on the RC supports by grafting and UV polymerization. The protein adsorption capacities of the prepared membranes were obtained through both the static binding capacity (SBC) and the dynamic adsorption capacity (DBC) measurement. As a result, the membrane chromatography with the smaller the pore size, the larger the surface area showed the highest protein adsorption capacity. Membrane chromatography which was prepared by using deacetylated commercial CA support with MAPTAC ligand (i.e., RC 0.8 + MAPTAC: 43.69 mg/ml, RC 3.0 + MAPTAC: 36.33 mg/ml) showed a higher adsorption capacity compared to commercial membrane chromatography (28.38 mg/ml).

• Proceedings of the Korean Environmental Sciences Society Conference
• /
• 2008.11a
• /
• pp.423-427
• /
• 2008

지하수 중에 함유된 불소이온을 제거하기 위한 흡착제로 상용의 음이온교환수지(PA), 란탄산화물(La) 및 수산화아파타이트(HAp)를 선정하고 각각의 흡착특성을 회분식 실험을 통해 검토하였다. 그 결과를 요약하면 다음과 같다. 1) PA, La 및 HAp의 불소흡착은 Fruendlich isodtherm model 및 Pseudo-second-order kinetics model과 일치하는 거동을 보였다. 2) D-R model로부터 구한 흡착에너지는 9.66$\sim$12.90 kJ/mol로 이온교환메커니즘을 나타내는 흡착에너지 6$\sim$16 kJ/mol의 범위에 속하였다. 3) Van't Hoff 식에 이용하여 구한 ${\Delta}H^{\circ}$ 및 ${\Delta}G^{\circ}$값은 각각 3.40$\sim$89.28 kJ/mol과 -12.26$\sim$-13.76 kJ/mol의 범위를 보여 모두 흡착과정이 발열반응이며 자발적으로 일어나는 조건임을 알 수 있었다. 4) PA는 pH 6$\sim$8인 중성영역에서 가장 높은 불소 제거율을 보였으며, La과 HAp는 산성영역으로 갈수록 불소 제거율이 증가하는 특성을 나타내었다. 5) 불소에 대한 흡착선택성은 La$\geq$HAp>PA 순으로 높았으며, La의 경우 불소를 제외한 모든 음이온에 대한 흡착능이 없을 정도로 불소에 대한 흡착 특이성을 보였다.

• 한국신재생에너지학회:학술대회논문집
• /
• 2006.11a
• /
• pp.525-528
• /
• 2006

아임계 및 초임계수에 의한 목질바이오매스의 당화특성을 분석하기 위하여 분해공정 동안 압력을 23MPa(물의 임계압력)로 고정하고 물의 아임계 온도$(325^{\circ}C,\;350^{\circ}C)$와 초임계 온도$(380^{\circ}C,\;400^{\circ}C,\;425^{\circ}C)$에서 현사시나무 목분을 각각 60초 동안 처리하였다. 생성된 현사시나무의 분해산물에는 액상과 고형분의 분해산물이 섞여 있었다. 각 처리조건에 따른 목질바이오매스의 분해율은 온도가 상승함에 따라 증가하였으며 초임계 온도인 $425^{\circ}C$에서 최고 83.1%의 분해율을 나타냈다. 아임계 및 초임계수에 의해서 생성된 단당류는 고성능 음이온 교환 크로바토그래프(HPAEC)를 이용하여 분석하였다. 목질바이오매스의 초임계수 분해과정에서 처리 온도가 높아지면서 단당류 수율은 증가하는 경향을 보였으며, $425^{\circ}C$에서 가장 높은 7.3%의 단당류 수율을 나타내었다. 아임계 온도 범위에서는 현사시나무의 섬유소 성분 중에서 자일란이 우선적으로 분해되어 자일로스의 생성비율이 비교적 높았으며, 처리온도가 높아지면서 셀롤로오스의 분해에 의한 글루코오스 생성율이 급격히 상승하였다. 이렇게 생성된 단당류 성분들은 고온의 반응조건하에서 열분해 반응에 의해서 더욱 분해되어 퓨란계 화합물로 변형되었다.