• Bulletin of the Korean Chemical Society
• /
• 제23권1호
• /
• pp.35-40
• /
• 2002

Photoreaction of guest organic anions in layered organic-inorganic hybrid materials was investigated. The layered hybrids were synthesized by an anion-exchange reaction of $[LiAl_2(OH)_6]Cl{\cdot}yH_2O$ layered double hydroxide with aqueous (Z,Z)- and (E,E)-muconates under inert atmospheric condition, to give new organicinorganic hybrids of $[LiAl_2(OH)_6]_2[(Z,Z)-C_6H_4O_4]{\cdot}zH_2O$ and $[LiAl_2(OH)_6]_2[(E,E)-C_6H_4O_4]{\cdot}H_2O$, respectively. The basal spacings calculated by XRPD of intercalates indicate that muconate anions have almost vertical arrangements against the host $[LiAl_2(OH)_6]^+$ lattices in the interlayer of organic-inorganic hybrid materials. When UV light was irradiated on the suspension of $[LiAl_2(OH)_6]_2[(Z,Z)-C_6H_4O_4]{\cdot}zH_2O$, the (Z,Z)-muconate anions of the gallery space of hybrids were polymerized in the aqueous media while it was isomerized into more stable (E,E)-muconate in the methanollic suspension in the presence of catalytic amount of molecular iodine. All the products were characterized using elemental analysis, TGA, XRPD, FT-IR, $^1H$ NMR and $^{13}C$ CP-MAS NMR.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2009년도 제38회 동계학술대회 초록집
• /
• pp.394-394
• /
• 2010

Ammonium ion (${NH_4}^+$) was suggested as the origin of interstellar $6.85\;{\mu}m$ band. Early study, in which organic molecule and water ice film mixtures were photolyzed so that organic acids could be produced, explained the generation of ${NH_4}^+$ from the reaction of photogenerated organic acid and ammonia ($NH_3$). However, the observed abundance of organic acids or their counter-anions are not so high in interstellar ice and not enough to protonate $NH_3$ into ${NH_4}^+$ in the observed level. Because of the shortage in photogenerated organic acids, the candidate of acid which protonates $NH_3$ should be modified. Here, we prepare $NH_3/H_2O$ binary mixtures and photolyze them with vacuum ultraviolet (VUV, peak at 10.6 and 10.0 eV). We find the ammonium ion (${NH_4}^+$) from photolyzed mixture by using low energy sputtering (LES) and reflection absorption IR spectroscopy (RAIRS). As a hydronium ($H_3O^+$) can be produced by UV irradiation and protonate bases, ${NH_4}^+$ may be formed from the reaction of photogenerated $H_3O^+$ and $NH_3$. We show the generation of ${NH_4}^+$ without any kind of organic molecules or acids, and it may explain the relatively high abundance of ${NH_4}^+$ compared to the counter-anions or organic acids in interstellar ice.

• 농업과학연구
• /
• 제23권2호
• /
• pp.250-260
• /
• 1996

Observed results of the adsorption between two competing anions for the shared sorption sites represent that the adsorption phenomena may depends on the characteristics of anion and available sorption sites in a given conditions. In binary systems, adsorption of one species can significantly influence the fate of the other anion, resulting in control of the extent of solute-adsorbate distributions throughout soil profile. And the proton-donation mechanisms by organic anions having a carboxyl as a functional group can also influence the adsorption of inorganic anions onto the hydroxylated sites of Fe and Al oxides. However, study of competitive adsorption of specifically adsorbed anions illustrates some of difficulties which arise in interpretation of reactions at oxide/aqueous solution interfaces. At least two factors prevented a simple analysis of reactions. First, at any pH value the maximum amount of adsorbate taken up at the surface depends on the identity of the anion. Second, it was necessary to postulate the sorption sites where the anion can be adsorbed. Hence, anions having non-specific adsorption characteristics are less capable for sorption sites, compared to those of specific adsorption characteristics, even though competition complies both ordinary and electrostatic interactions for sorption sites. Therefore, competition among chemical species in soil matrix can be of major significance in determining the effective mobility of any reactive anions with sorption sites.

• Korean Chemical Engineering Research
• /
• 제46권2호
• /
• pp.436-442
• /
• 2008

수용액에서 음이온을 제거하기 위하여 다양한 종류의 유기/무기 복합음이온교환수지를 제조하였다. 제조된 음이온교환수지들은 질소흡탈착 실험, 적외선분광실험, 원소분석 등을 통하여 그 특성을 조사하였다. 또한 제조된 음이온교환수지의 음이온 교환 특성을 조사하기 위하여 배치(batch) 실험과 키네틱(kinetic) 실험을 수행하였다. 제조된 시료들 가운데 트리메틸암모늄 기능기를 사용했을 때보다 트리부틸암모늄 기능기를 사용하였을 때 더욱 큰 흡착량을 나타내었는데, 이것은 호프마이스터 효과와도 부합된다. 또한, 소수성기를 다량 보유하고 있는 계면활성제인 헥사데실아민도 소수성 음이온에 대한 교환능이 있는 것을 알 수 있었다.

• 대한화학회지
• /
• 제32권2호
• /
• pp.113-121
• /
• 1988

역상 액체 크로마토그래피에 의한 방향족 슬폰산 및 카르복시산들의 머무름 기구와 분리를 브롬화 도데실트리메틸 암모늄(DTAB)을 포함하는 이동상에서 연구하였다. 머무름 기구는 DTAB가 정지상에 일차층을 형성하고 반면 음이온 시료와 이동상에 존재하는 다른 공존 음이온들이 경쟁적으로 이차층을 형성하는 이온-상호작용 모델임을 확인하였다. 시료들의 용량인자들은 pH, 여러 유기 용매들의 농도, 이동상에 존재하는 공존 음이온 및 시료의 작용기 등 여러 인자들에 의해 영향을 받았다. 그리고 몇 가지 유기 혼합시료들을 최적 조건하에서 상호 분리를 시도하였다

• 한국염색가공학회:학술대회논문집
• /
• 한국염색가공학회 2011년도 제45차 학술발표회
• /
• pp.34-34
• /
• 2011

Recently, people have concerned about environmental pollution. This environmental pollution occur due to many reasons such as heavy metal ions and anions. In this regard, many researchers have studied organic materials to monitor above reasons to protect environmental pollution. One of the organic materials for this function is chemosensor. This chemosensor has been studied and reported about monitoring toxic heavy metal ions and anions. In this study, the dye sensor was designed and synthesized through reaction of Rhodamine 6G and 1,3-Indanedion. this dye sensor selective detected $Hg^{2+}$ metal ions while showing red color absorption and yellowish-green strong fluorescence emission compared to other heavy metal ions such as $Cu^{2+}$, $Hg^{2+}$, $Ag^{2+}$, $Zn^{2+}$, $Fe^{2+}$ and $Fe^{3+}$. In this regard, we anticipated that this dye senosr can provide an significant material for monitoring mercury which cause environmental pollution. Thus, We investigated detailed properties of this dye sesnor with using UV-Vis absorption and fluorescent spectrophotometer, Job's plot method for metal binding complex, computational simulated calculation named Material Studio 4.3 suite to approach for electron distribution and HOMO/LUMO.

• 공업화학
• /
• 제32권2호
• /
• pp.190-196
• /
• 2021

저품질 석회석의 탈황 성능 개선을 알아보기 위해 초산, 젖산, 개미산 등 3종의 유기산 첨가제를 사용하여 기포형 반응기에서 탈황 반응을 수행하였다. 유기산이 첨가되지 않은 석회석 슬러리는 pH 5.2 이하에서 초기 탈황 효율의 저하가 일어났다. 반면, 유기산이 첨가된 석회석 슬러리는 pH 4.2~4.5에서 안정된 초기 탈황 효율을 나타내었다. 슬러리 pH 4 이하에서 유기산이 첨가된 석회석 슬러리의 탈황 성능은 유기산의 해리에 의해 생성된 음이온의 양과 연관될 수 있다. 슬러리 중 유기산의 음이온 양이 많으면 슬러리 pH의 완충 기능 저하가 급격히 일어나지 않았다. 이와 같은 결과들은 유기산의 산성도 및 해리도에 기인하였다. 3종의 유기산 첨가에 따른 저품질 석회석 슬러리의 탈황 성능 증가율은 초산(2.6%) < 젖산 (6.4%) < 개미산 (16.7%) 순으로 나타났다.

• Journal of Pharmaceutical Investigation
• /
• 제23권3호spc1호
• /
• pp.41-50
• /
• 1993

The iontophoretic delivery across rat skin of quaternary ammonium salts (isopropamide: ISP, pyridostigmine: PS), which are positively charged over a wide pH range, was measured ill vitro. The study showed that: (a) iontophoresis significantly enhanced delivery of ISP and PS compared to respective passive transport; (b) delivery of ISP and PS was directly proportional to the applied continuous direct current density over the range of $0-0.69\;mA/cm^2;$ (c) delivery of ISP and PS was also proportional to the drug concentration in the donor compartment over the range of $0-2{\time}l0^{-2}M:$ (d) sodium ion in the donor compartment inhibited the drug transport possibly due to decreasing the electric transference number of the drug; (e) delivery of ISP and PS increased as the pH of the donor solution increased over the pH range 2-7 suggesting permselective nature of the epidermis, and inhibition of the transference number of the drugs by hydronium ion; (f) some organic anions such as taurodeoxycholate, salicylate and benzoate which form lipophilic ion-pair complexes with ISP inhibited the delivery of ISP. The degree of inhibition by the organic anions was linearly proportional to the extraction coefficient $(K_e)$ of ISP from the partition system with each counteranion between phosphate buffer (pH 7.4) and n-octanol. For PS, however, taurodeoxycholate, but not salicylate and benzoate inhibited the iontophoretic delivery. It suggests that not only sodium ion and hydronium ion but also the counteranions which form lipophilic ion-pairs with quaternary ammonium drugs are not favorable components in formulating the donor solution of the drugs to achieve an effective iontophoretic delivery.

• 환경위생공학
• /
• 제8권2호
• /
• pp.99-108
• /
• 1993

It is well known that we should take 2L of drinking water per day to maintain our health. The drinking water quality is becoming worse owing to sewage discharge and industrial wastewater. Surface water is polluted by various kinds of contaminants and ground water were known as clean and unpolluted water, but through recent many reports the ground waters are also contaminated by waste disposal and intrusion of organic and bacterial movement. This research was undertaken to make a water index of water contamination by referringcations cations and anions. NH$_{4}$, Fe, Mn, and Pb are chosen as cations and $NO_3$, Cl, and $SO_4$ ions are chosen as anions to make a index, and the following water index was made as the contamination index. (Fe+Mn+Pb)/0.7+$(NH_4+NO_3+Cl+SO_4)$/10.5<6.0 By using ton Chromatography the cations and anions are rapidly analyzed and plotting the analyzed data to the equation, we can easily get the degree of contaminations by avoiding analysis of over 37 water parameters in several days. Of course this index of water contamination is not perfect and detail one, but in case of emergent case or to know the overall trends of contamination, it is convenient to use this index. Among the tested 5 kinds of samples the ground water showed contamination index of 6.87. Authors used the already published healthy index and tasty index and differentiated their degrees in detail.

• 분석과학
• /
• 제8권1호
• /
• pp.33-40
• /
• 1995

미량의 hydroxide 이온은 Tetra-n-Butyl Ammonium(TBAC)에 의해 수액상에서 유기상으로 추출될 수 있다. 일차 알코올류, 특히 다이올류의 적은 양을 첨가하면 상전이 촉매계의 거동이 급격히 변하고 과량의 염기를 유기상에서 발견할 수 있다. 정량 측정은 유기상에서 1차, 2차 알콕사이드와 다이올 음이온들의 추출한 양에 대해 행하였다. 한편, 일차 알코올류와 벤질 알코올의 추출에 대한 선택상수들은 수액상과 유기상에서 $Q^+RO^-$($Q^+$ : quaternary 양이온, $RO^-$ : 알콕사이드 이온)와 $Q^+Cl^-$과 같은 이온쌍들의 평형상수와 이 두 상간의 분배계수로 분리되었다. 따라서 $Q^+RO^-$의 선택성에 대한 전제 특성을 본 연구결과에서 언급된 여러 상수들에 대하여 자유에너지에 상응하는 값들을 사용해서 더욱 상세하게 논하였다.