• Title/Summary/Keyword: 이온교환반응

Search Result 503, Processing Time 0.025 seconds

Selectivity Characteristics for Equilibrium and Column Anion Exchanges (음이온 평형 및 칼럼교환 선택도 특성)

  • 이인형;이석중
    • Proceedings of the KAIS Fall Conference
    • /
    • 2002.05a
    • /
    • pp.137-139
    • /
    • 2002
  • 이온교환은 액체상 이온과 고체상 이온간의 화학반응이며 연수 및 탈염공정, 특정물질의 제거 및 회수, 토양을 통한 이온성 물질의 이동에서 널리 이용되고 있다. 이온교환수지는 이온교환시 원자가가 높을수록, 수화반경이 작을수록, 이온농도가 낮을수록 증가한다. 본 연구는 이온교환수지에 대한 평형실험을 선택도가 칼럼실험에 적용되는지 조사하였다. 이 실험치 결과에서 음이온 교환수지의 선택도 순서는 OH/sup -/ < F/sup -/ < HCO₃/sup -/ < Cl/sup -/ < Br/sup -/ ≤ No₃/sup -/ < So₄/sup 2-/ 이였으며, 음이온 칼럼 교환도 동일하였다. 또한 바탕 양이온의 가수가 높을수록 이온교환이 빠르게 진행됨을 알 수 있다.

Selective Disproportionation of Toluene over Various Cation-exchanged ZSM-5 Catalysts (양이온 교환된 ZSM-5 촉매상에서 톨루엔의 선택적인 반응)

  • Jong Shin Yoo;Byoung Joon Ahn;Hakze Chon
    • Journal of the Korean Chemical Society
    • /
    • v.27 no.2
    • /
    • pp.127-132
    • /
    • 1983
  • The catalytic activity of ZSM-5 catalyst for the disproportionation of toluene is dependent on the type of cation exchanged, the degree of ion-exchange and the reaction temperature. The activity increases in the order of alkaline-, alkali earth-, hydrogen, and rare-earth-exchanged ZSM-5 and decreases with increasing degree of cation exchange. Among the ion-exchanged ZSM-5 catalyst, only Cs-ZSM-5 shows predominant selectivity for p-xylene. The selectivity increases with increasing degree of $Cs^+$-exchange and decreasing reaction temperature. This phenomenon is interpreted in terms of shape selectivity arising from the partial blocking of channel intersections by large cesium ions.

  • PDF

The Calcium and Magnesium Ion-Exchange Properties of Snythetic δ-Na2Si2O5 from Water Glass (Water Glass로부터 합성한 δ-Na2Si2O5의 Ca2+, Mg2+ 이온교환성)

  • Jeong, Soon-Yong;Suh, Jeong-Kwon;Park, Jeong-Hwan;Doh, Myung-Ki;Koh, Jae-Cheon;Lee, Jung-Min
    • Applied Chemistry for Engineering
    • /
    • v.5 no.3
    • /
    • pp.406-412
    • /
    • 1994
  • The ion-exchange properties of $Ca^{2+}$ and $Mg^{2+}$ ions have been studied in ${\delta}-Na_2Si_2O_5$ synthesized from water glass. Results show that optimum temperature for synthesis of ${\delta}-Na_2Si_2O_5$ was $725^{\circ}C$. Ion-exchange isotherms for $Ca^{2+}$ and $Mg^{2+}$ exchange for $Na^+$ in the synthetic ${\delta}-Na_2Si_2O_5$ show that the ion-exchange capacity of magnesium is better than that of calcium, and the ion-exchange of magnesium is less sensitive for temperature than that of calcium. When initial pH of solution is increased between 2 and 6, the ion-exchange capacities of magnesium and calcium decrease a little. However, they are almost constant above pH 6 because of alkali buffer effect of ${\delta}-Na_2Si_2O_5$. In the thermodynamic studies, it was found that Gibbs free energies of reaction of calcium ion-exchange are larger than those of magnesium ion-exchange with inverse order of selectivity. The standard enthalpy and entropy of reaction of calcium ion-exchange are larger than those of magnesium ion-exchange.

  • PDF

A Study of Intercalations-complex of Montmorillonite as Model-system (III) (Model-system으로서의 몬트모릴로나이트의 층간화합물에 관한 연구 (III))

  • 조성준
    • Journal of the Korean Ceramic Society
    • /
    • v.38 no.5
    • /
    • pp.431-437
    • /
    • 2001
  • 본 연구에서는 양이온 교환반응에 의해 Na-Mont와 R$_{11}$SO$_4$로부터 R$_{11}$SO$_4$-Mont 층간화합물을 합성한 후, 이 R$_{11}$SO$_4$-Mont 층간화합물을 다시 제 4차 유기 양이온인 (Et)$_4$N$^{+}$ 이온 및 (Bu)$_4$N$^{+}$ 이온과 반응시켜 그 거동을 살펴보았다. R$_{11}$SO$_4$-Mont를 (Et)$_4$N$^{+}$이온과 반응시켰을 대보다 (Bu)$_4$N$^{+}$ 이온과 반응시킨 경우에 좀 더 큰 층간거리가 얻어졌다. R$_{11}$SO$_4$-Mont를 (Et)$_4$N$^{+}$이온 및 (Bu)$_4$N$^{+}$과 반응시켜 얻은 층간화합물을 다시 아세토니트릴, 에탄올 및 디옥산과 팽윤반응을 수행한 결과 층간거리가 확장되었으나, 이는 Na-Mont를 R$_{11}$SO$_4$와 48시간 교환 반응시킨 후에 교환용액 하에서 얻은 R$_{11}$SO$_4$-Mont의 층간거리에 불과했다. 원소분석결과, R$_{11}$SO$_4$-Mont와 (Bu)$_4$N$^{+}$를 반응시킬 경우 반응이 반응식 b에 의거 진행되고, (Bu)$_4$N-Mont를 R$_{11}$SO$_4$와 반응시킬 경우에는 반응식 c에 의거 진행됨을 예측할 수 있었다.의거 진행됨을 예측할 수 있었다.

  • PDF

Synthesis of Multifunctional Polypropylene-g-(acrylic acid/styrene) Fibrous Ion Exchanger by Electron Beam and Adsorption Properties of Lithum Ion (전자선 조사에 의한 다관능 Polypropylene-g-(acrylic acid/styrene) 섬유상 이온교환체의 합성과 리튬이온 흡착특성)

  • 황택성;박진원;이재천
    • Polymer(Korea)
    • /
    • v.24 no.6
    • /
    • pp.763-769
    • /
    • 2000
  • The multifunctional cation exchangers, sulfonated polypropylene-g-(acrylic acid/styrene) [PP-g-(AAc/Sty)] were synthesized by the irradiational grafting of AAc and Sty onto PP staple fabric with electron beam accelerator and its subsequent sulfonation. The highest degree of grafting obtained was 190% at a monomer mixture of 30 vol% AAc: 70 vol% Sty and a solvent mixture of 30 vol% water : 70 vol% methanol and the degree of grafting decreased with an increase of the AAc content in the monomer mixture at constant solvent content. Maximum ion exchange capacity of the copolymer was 4.6 meq/g. The Li$^{+}$ adsorption ability of the copolymer synthesized in the study was the best among PP-g- AAc, sulfonated PP-g-Sty, and sulfonated PP-g-(AAc/Sty).).

  • PDF

철 이온이 도입된 수산화인회석의 합성과 물성변화에 관한 연구

  • Jeong, Byeong-Hyeon;Gwon, Gi-Yeong
    • Proceedings of the Korean Vacuum Society Conference
    • /
    • 2013.02a
    • /
    • pp.285-285
    • /
    • 2013
  • 수산화인회석(Hydroxyapatite, HAP)은 인체 내 뼈와 치아의 주성분으로서 칼슘과 인산염으로 구성된 물질이다. 암모늄을 이용하여 pH를 조절함으로서 hexagonal 형태의 HAP를 수열합성법으로 합성하였다. XRD pattern을 통하여 수산화인회석의 결정구조를 확인하였으며, 전이금속 중의 하나인 Fe(III) 이온을 이온교환반응을 통하여 수산화인회석 표면에 도입하였다. ICP 측정을 통해 Fe 함량을 정량하였고 SEM과 TEM image를 통하여 크기와 형태를 관찰하였다.

  • PDF

이온교환에 의한 Silica 제거능 연구

  • Yun, Tae-Gyeong;Lee, Gang-Chun;No, Byeong-Il
    • 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.

  • PDF

Methanol-to-Olefin Conversion over UZM-9 Zeolite: Effect of Transition Metal Ion Exchange on its Deactivation (UZM-9 제올라이트에서 메탄올의 올레핀으로 전환반응: 전이금속 이온 교환이 촉매의 활성저하에 미치는 영향)

  • Kim, Sun Jung;Jang, Hoi-Gu;Seo, Gon
    • Korean Chemical Engineering Research
    • /
    • v.51 no.2
    • /
    • pp.181-188
    • /
    • 2013
  • The effect of transition metal ion exchange into UZM-9 zeolite with LTA framework on its deactivation in methanol-to-olefin (MTO) conversion was discussed. The ion exchange of copper, cobalt, nickel, and iron did not induce any notable change in the crystallinity, crystal morphology, and acidity of UZM-9. The small cage entrance of UZM-9 caused the high selectivity to lower olefins in the MTO conversion, while its large cages allowed the rapid further cyclecondensation of active intermediates, polymethylbenzenes including hexamethylbenzene, resulting in a rapid deactivation. The UZM-9 containing copper and cobalt ions showed considerably slow deactivations. The interaction between transition metal ions and polymethylbenzene cation radicals, the active intermediates, generated in the MTO conversion stabilized the radicals and slowed down the deactivation of UZM-9.

Shape Selective Catalysis of Cation-Exchanged Pentasil Zeolites (양이온 교환된 펜타실 제올라이트의 형상 선택적 촉매작용)

  • Byoung Joon Ahn;Byung Woo Hwang;Hakze Chon
    • Journal of the Korean Chemical Society
    • /
    • v.28 no.1
    • /
    • pp.62-69
    • /
    • 1984
  • The reaction of toluene with ethanol was studied over various cation-exchanged pentasil zeolite catalysts. The toluene disproportionation reaction to produce xylenes increased with increasing reaction temperature and the activity of alkylation of toluene with ethanol showed maximum at around $400^{\circ}C$. Only Cs-ZSM-5 catalyst showed pronounced p-ethyltoluene selectivity increasing to 96% with increasing degree of Cs-exchange. The sorption rate of m-xylene was lower for Cs-exchanged ZSM-5 than H-ZSM-5 catalyst. These phenomena were interpreted in terms of shape selectivity arising from the partial blocking of channel intersections by large cesium ions.

  • PDF

Kationenaustauscher auf Basis von p-carboxystyrolhaltigen Copolymeren (p-Carboxystyrol계 양이온 교환 수지)

  • Kim, Un-Young
    • Journal of the Korean Chemical Society
    • /
    • v.14 no.1
    • /
    • pp.19-27
    • /
    • 1970
  • Durch Umsetzung von vernetzten p-jodstyrolhaltigen Coplymeren mit benzolischer Butyllithiumlosung und durch anschließende Carboxylierung mit gasformigem Kohlendioxid lassen sich p-carboxystyrolhaltige Copolymere herstellen. Die erreichbare Kapazitat der erhaltenen Harze betragt etwa 2,5 bis 2,8 mval/g. Aus den Titrations-nskurven erhahlt man einen scheinbaren $pK_a$-Wert von 8,07 fur das normal hergestellte und von 7,75 fur das toluolmodifizierte Harz. Der Austauscher nimmt Kaliumoinen im alkalischen Gebiet auf. Das Gleichgewicht des Harzes mit Calciumionen stellt sich bei pH = 6 bei ca. 85% Austausch ein. Dagegen nimmt das Harz Kupferionen bei pH = 4 bis 5 in der Außenlosung bis zu 100% auf.

  • PDF