• Corrosion Science and Technology
• /
• 제7권4호
• /
• pp.212-218
• /
• 2008

Inorganic ion exchange compounds (IECs) including hydrotalcites and bentonite clays are a well known classes of layered mixed metal hydroxides or silicates that demonstrate ion exchange properties. These compounds have a range of applications from water purification to catalyst supports. The use of synthetic versions of these compounds as environmentally friendly additives to paints for storage and release of inhibitors is a new and emerging application. In this paper, the general concept of storage and release of inhibiting ions from IEC-based particulate pigments added to organic coatings is presented. The unique aspects of the IEC structure and the ion exchange phenomenon that form the basis of the storage and release characteristic are illustrated in two examples comprising an anion exchanging hydrotalcite compound and a cation exchanging bentonite compound. Examples of the levels of corrosion protection imparted by use of these types of pigments in organic coatings applied to aluminum alloy substrates is shown. How corrosion inhibition translates to corrosion protection during accelerated exposure testing by organic coatings containing these compounds is also presented.

• 한국연초학회지
• /
• 제26권2호
• /
• pp.159-167
• /
• 2004

This work has been conducted to select appropriate filter materials for removing carbonyl compounds in mainstream tobacco smoke. To investigate of the usability of this filter materials, two types of bead ion exchangers were synthesized and their adsorption characteristics for carbonyl compounds were investigated. Sulfonic acid group-containing cation exchanger and ammonium group-containing anion exchanger were synthesized by the suspension polymerization of glycidylmethacrylate(GMA) and divinylbenzene(DVB) followed by the subsequent functionalization, respectively. The removal efficiency of carbonyl compounds by these two ion exchangers increased in the presence of moisture. However, the amount of carbonyl compounds adsorbed on the anion exchanger was larger than that on the cation exchanger under two levels of water contents tested. This phenomenon seems to arise from the electron delocalization in carbonyl group of the anion exchangers. There was not any significant relationship between the amount of carbonyl compounds adsorbed on ion exchangers and the length of adsorption column. From the large ion exchange capacity and rapid ion exchange reaction rate of the anion exchanger, it is suggested that the anion exchanger may be a good filter material for removing carbonyl compounds in the mainstream tobacco smoke.

• 폴리머
• /
• 제29권1호
• /
• pp.74-80
• /
• 2005

담배 주류연 중 카보닐 화합물의 감소를 위한 필터 물질로 비드 형상의 양이온 및 음이온교환체를 glycidylmethacrylate(GMA)와 d9ivinylbenzene(DVB)의 현탁중합에 의해 중합체를 합성한 후 설폰화 반응 및 아민화 반응에 의해 합성하였다. 합성한 이온교환체의 구조는 FT-IR/ATR을 이용하여 확인하였으며 SEM을 이용하여 주류연 흡착에 따른 이온교환체의 표면을 관찰하였다. 또한 이온교환용량, 관능화율 및 담배 주류연 중 카보닐 화합물의 흡착 특성을 확인하였다. 관능화율과 이온교환용량은 공단량체 중 DVB의 함량이 5 wt%에서 최대를 나타내었다. 이온교환체에 의한 담배 주류연 중 카보닐 흡착량은 카보닐기 내의 전자 편재화에 의한 음이온교환반응이 더 용이하여 음이온교환체에서 더 높게 나타났으며, 수분 존재 시 더 많은 흡착량을 나타내었다. 또한 짧은 접촉 시간에서도 높은 흡착량을 가지고 있어 궐련 필터의 적용 가능성을 확인할 수 있었다.

• 한국환경과학회지
• /
• 제22권8호
• /
• pp.1009-1017
• /
• 2013

Perfluorooctanoic acid (PFOA) and perfluorooctyl sulfonate (PFOS) is a new persistent organic pollutants of substantial environmental concern. This study investigated the potential of magnetic ion exchange resin (MIEX$^{(R)}$) as the adsorbent for the removal of PFOA and PFOS from Nakdong River water. In our batch experiments, we studied the effect of some parameters (pH, temperature, sulfate concentration) on the removal of PFOA and PFOS. The results of sorption kinetics on MIEX$^{(R)}$ show that it takes 90 min to reach equilibrium but the economical contact time and dosage were 30 min and 10 mL/L. An increase in pH (pH 6~10) leads to a decrease in PFOA (2.0%) and PFOS (3.6%) sorption on MIEX$^{(R)}$. The sorption of both PFOA and PFOS decreases with an increase in ionic strength for sulfate ion (${SO_4}^{2-}$), due to the competition phenomenon. An increase in water temperature ($8^{\circ}C{\sim}28^{\circ}C$) in water leads to a increase in PFOA (2.8%) and PFOS (4.3%) sorption on MIEX$^{(R)}$. Based on the sorption behaviors and characteristics of the adsorbents and adsorbates, ion exchange and hydrophobic interaction were deduced to be involved in the sorption, and hemi-micelles possibly formed in the intraparticle pores.

• Environmental Sciences Bulletin of The Korean Environmental Sciences Society
• /
• 제10권S_2호
• /
• pp.79-88
• /
• 2001

Humic acids react with chlorine to produce Trihalomethanes(THMs), known as carcinogens, during disinfection, the last stage in water purification. Currently, the removal of organic humic acids is considered the best approach to solve the problem of THM formation. Accordingly, the current study examined the adsorption of organic compounds of humic acids onto an inorganic carrier prepared from oyster shell waste. The adsorbent used was activated oyster shell powder(HAP) and silver ion-exchanged oyster shell powder(HAP-Ag), with CaCO$_3$ as the control. The adsorbates were phthalic acid, chelidamic acid, catechol, dodecylpyridinium chloride(DP), and 2-ethyl phenol(2-EP). The adsorption experiments were carried out in a batch shaker at $25^{\circ}C$ for 15 hours. The equilibrium concentration of the adsorbate solution was analyzed using a UV spectrophotometer and the data fitted to the Langmuir isotherm model. Since the solution pH values were found to be greater than the pKa values of the organic compounds used as adsorbates, the compounds apparently existed in ionic form. The adsorptive affinities of the organic acid and phenolic compounds varied depending on the interaction of electrostatic forces, ion exchange, and chelation. More carboxylic acids and catechol, rather than DP and 2-EP, were adsorbed onto HAP and HAP-Ag. HAP and HAP-Ag exhibited a greater adsorptive affinity for the organic compounds than CaCO$_3$, used as the control.

• 에너지공학
• /
• 제27권2호
• /
• pp.70-80
• /
• 2018

Natural organic matter (NOM) is among the most common pollutant in underground and surface waters. It comprises of humic substances which contains anionic macromolecules such as aliphatic and aromatic compounds of a wide range of molecular weights along with carboxylic, phenolic functional groups. Although the concentration of NOM in potable water usually lies in the range of 1-10 ppm. Conventional treatment technologies are facing challenge in removing NOM effectively. The main issues are concentrated to low efficiency, membrane fouling, and harmful by-product formation. Ion-exchangers can be considered as an efficient and economic pretreatment technology for the removal of NOM. It not only consumes less time for pretreatment but also resist formation of trihalomethanes (THMs), an unwanted harmful by-product. This article provides a comprehensive review of ion exchange processes for the removal of NOM.

• Korean Chemical Engineering Research
• /
• 제53권4호
• /
• pp.463-467
• /
• 2015

We investigated catalytic activity of ion-exchange resins in acetalization of 1,2-propylene glycol with acetaldehyde. The impacts of reaction variables, such as temperature, reaction time, catalyst loading and feedstock composition, on the conversion of 1,2-propylene glycol were measured. The life of the catalyst was also studied. Furthermore, the reaction kinetics of 1,2-propylene glycol acetalization was studied. It was found that reaction rate followed the first-order kinetics to acetaldehyde and 1,2-propylene glycol, respectively. Therefore, overall acetalization reaction should follow the second-order reaction kinetics, expressed as. Key words: 1,2-propylene Glycol, 2,4-dimethyl-1,3-dioxolane, Ion-exchange Resin, Polyhydroxy Compounds, Acetalization $r=kC^{nA}_AC^{nB}_B=19.74e^{\frac{-6650}{T}}C^1_AC^1_B$.

• KSBB Journal
• /
• 제24권5호
• /
• pp.415-419
• /
• 2009

본 연구에서는 리그노셀룰로스 가수분해물과 유사한 조성을 갖는 합성 용액을 이용하여 무독화 실험을 진행하였다. 생물학적 무독화 방법으로는 peroxidase와 laccase와 같은 효소를 이용하였고, 이온교환과 흡착과 같은 물리화학적 방법으로는 이온교환수지와 활성탄을 이용하였다. 효소 중 peroxidase는 페놀계 화합물의 제거에 탁월한 효율을 보였으며, 5-HMF와 furfural은 활성탄에 의해 거의 모두 제거되었고, 아세트산은 음이온교환수지를 사용하는 것이 가장 효율적이었다. 활성탄과 이온교환수지는 다소간의 당손실을 일으켰다. 무독화 방법은 당화액에 포함되어 있는 저해물질의 조성을 고려하여 결정되어야 한다.

• Biomolecules & Therapeutics
• /
• 제6권4호
• /
• pp.364-370
• /
• 1998

Glycosidase inhibitors from urine of Bombyx mori were isolated and their inhibitory activities on glycosidases were evaluated. Six compounds were isolated by using several ion exchange columns, and their chemical structures were identified by the physicochemical and spectral data. Compound IV, V and Ⅵ were identified as 1-deoxynojirimycin, fagomine and 1,4-dideoxy-1,4-imino-D-arabinitol, respectively. Among six compounds isolated,1-deoxynojirimycin(IV) was the most potent inhibitor on $\alpha$-glucosidase and $\beta$-galactosidase of rat intestine, and its inhibitory activities for trehalase and almond $\beta$-glucosidase were relatively weak. Compound V and Ⅵl retained a little inhibitory potency toward $\alpha$-glucosidase and $\beta$-galactosidase. Compound II and III, however, have been found to have no effect on all glycosidases tested in this study.

• 멤브레인
• /
• 제12권3호
• /
• pp.143-150
• /
• 2002

전기투석은 이온성 물질을 분리하고 농축하는데 안정하고 효과적인 공정으로 알려져 있다. 그러나 전기투석 공정은 고가의 이온교환막 때문에 실제 공정에 적용하는데 많은 제한을 받아오고 있다. 따라서 전기 투석공정의 운전 전류밀도를 가능한 높게 공급함으로써 이온교환막의 단면적당 flux를 증가시켜 주어야 한다. 그러나 실제 공정의 운전에 있어서 운전 전류밀도는 이온교환막 표면에서의 농도분극 현상으로 제한을 받게 된다. 본 총설에서는 이온교환막을 통한 이온의 이동현상을 설명하고 전류-전압 곡선을 이용한 막특성 분석을 소개하였다. 또한 한계전류밀도 전후의 전류 영역에서 농도분극 현상과 동반하는 전기대류(Electroconvection), 물 분해 현상 등에 대한 최근 연구결과를 정리하였다.