• Bulletin of the Korean Chemical Society
• /
• 제30권9호
• /
• pp.1996-2000
• /
• 2009

Alkali metal salts were introduced to enhance the ionization efficiency of glucose and maltooligoses in electrospray ionization-mass spectrometry (ESI-MS). A mixture of the same moles of glucose, maltose, maltotriose, maltotetraose, maltopentaose, maltohexaose, and maltoheptaose was used. Salts of lithium, sodium, potassium, and cesium were employed as the cationizing agent. The ionization efficiency varied with the alkali metal cation types as well as the analyte sizes. Ion abundance distribution of the [M+$cation]^+$ ions of the carbohydrates varied with the fragmentor voltage. The maximum ion abundance at low fragmentor voltage was observed at maltose, while the maximum ion abundance at high fragmentor voltage shifted to maltotriose or maltotetraose for Na, K, and Cs. Variation of the ionization efficiency was explained with the hydrated cation size and the binding energy of the analyte and alkali metal cation.

• 한국수소및신에너지학회논문집
• /
• 제28권4호
• /
• pp.331-337
• /
• 2017

Proton Exchange Membrane Water Electrolysis (PEMWE) is one of the most popular and widely used methods for hydrogen production. PEMWE contributes to eco-friendly system via its energy storage system application, hence making it environmentally friendly to use. However, its main drawback is contamination of proton exchange membrane during water electrolysis. Existing cation such as magnesium, calcium and the likes are the cause for membrane contamination. As a result, the cation contamination give rise to degradation of performance of electrolysis and the reverse electrolysis is effective method to remove cation.

• The Korean Journal of Physiology and Pharmacology
• /
• 제5권2호
• /
• pp.107-122
• /
• 2001

A function of the kidney is elimination of a variety of xenobiotics ingested and wasted endogenous compounds from the body. Organic anion and cation transport systems play important roles to protect the body from harmful substances. The renal proximal tubule is the primary site of carrier-mediated transport from blood into urine. During the last decade, molecular cloning has identified several families of multispecific organic anion and cation transporters, such as organic anion transporter (OAT), organic cation transporter (OCT), and organic anion-transporting polypeptide (oatp). Additional findings also suggested ATP-dependent organic ion transporters such as MDR1/P-glycoprotein and the multidrug resistance-associated protein (MRP) as efflux pump. The substrate specificity of these transporters is multispecific. These transporters also play an important role as drug transporters. Studies on their functional properties and localization provide information in renal handling of drugs. This review summarizes the latest knowledge on molecular properties and pharmacological significance of renal organic ion transporters.

• 한국방사성폐기물학회:학술대회논문집
• /
• 한국방사성폐기물학회 2005년도 추계 학술대회 논문집
• /
• pp.79-86
• /
• 2005

In PSR on the Kori 3&4 NPP, The low level radioactive waste resin from SGBD demineralizer is more than $65\%$ of total waste resin in NPP So, it needs to be improved. The secondary cooling water pH control methods are used ammonia-AVT from the first. According to changing ETA which is better than ammonia, SGBD cation load is increased about 2-3 times. Waste resin product is also increased in proportion to the SGBD cation load. To reduce the waste volume, new cation resin exchange criteria is confirmed that demineralizer is almost saturated.

• Bulletin of the Korean Chemical Society
• /
• 제26권9호
• /
• pp.1335-1338
• /
• 2005

Thianthrene cation radical perchlorate ($Th^{+{{\cdot}}}{ClO_4}^-$) reacted readily with two isomeric thiols, benzylthiol (1) and 4-methylbenzenethiol (7) in an acetonitrile solution at room temperature. From the reaction of 1, the major products, N-benzylacetamide (4) and benzyl sulfide (5), are characteristic of benzyl carbocations while the minor one, benzyl disulfide (6) implies free radical component of the reaction. It is unprecedented that the formation of a benzyl carbocation was caused by the extrusion of sulfur atoms from benzyl sulfur cations (3). In contrast, from the reaction of 7, only p-tolyl disulfide (10) was obtained from both sulfur radicals and cations. In the reaction of 7 the thio-extrusion was not observed from the p-tolyl sulfur cation (9). A thianthrene cation radical ($Th^{+{{\cdot}}}$) was reduced quantitatively to thianthrene (Th) in both reactions.

• 한국자기공명학회논문지
• /
• 제6권2호
• /
• pp.103-112
• /
• 2002

The photoproduced cation radical of N-methylphenothiazine $(PC_1)$ doped into phenyltriehtoxysilane (PhiTEOS), vinyltriethoxysilane (VTEOS) and methyltriethoxysilane (METOS) was studied with electron spin resonance (ESR) and electron nuclear double resonance (ENDOR). The photoinduced charge separation efficiency was determined by integration of ESR spectra which correspond to the amount of photoproduced cation radical in the matrices. This was correlatively studied with the polarity and pore size of the gel matrices. The relative polarity of the matrices was determined by measuring ${\lambda}_{max}$ values of $PC_1$ in the different matrices. The relative pore size among the matrices was determined by measuring relative proton matrix ENDOR line widths of the photoproduced cation of $PC_1$. The decay kinetic constants of the cation radical of $PC_1$ in the different matrices with relatively studied with fitting the biexponential decay curves after exposure at the ambient condition. This is correlatively interpreted with the polarity and pore size of the matrices.

• Bulletin of the Korean Chemical Society
• /
• 제1권3호
• /
• pp.98-101
• /
• 1980

For the first time we have synthesized thiabenzene radical by the reaction of thiopyrylium cation with alkali metals. As might be expected for a free radical, ESR-spectrum of 2,4,6-triphenylthiabenzene radical shows the single signal with g-value of 2.0045. The proton signal of 2,4,6-triphenylthiabenzene radical in nmr spectrum shifts to the higher field than that of 2,4,6-triphenylthiopyrylium cation by ca. 0.5 ppm. From the UV-spectrum of thiabenzene radical the presence of 6${\pi}$ non-benzenoid aromatic system was observed as in the case of thiopyrylium cation. The reactivity of alkali metals with thiopyrylium cation increases in the order of decreasing ionization energy, Li

• Bulletin of the Korean Chemical Society
• /
• 제10권2호
• /
• pp.132-133
• /
• 1989

To probe the geometrical effects of cyclopropyl moiety on the stabilization of an adjacent cation center, chemical shift of 2-p-fluorophenyl-8,9-dehydro-2-adamantyl cation (3) was compared with that of 5-p-fluorophenyl-2,4-dehydro-5-homoadamantyl cation (4). Difference between the chemical shift of 8,9-dehydro-2-adamantyl cation 3 and that of 2,4-dehydro-5-adamantyl cation 4 is 5.1 ppm (${\Delta}{\Delta}{\delta}$). We conclude, therefore, that ion 3 is about 3.82 kcal more stadble than ion 4 of which rigid carbon skeleton requires significant distortion of the cyclopropane ring from the ideal bisected conformation. The energy difference between these cations can be calculated by Taft-Relationship$^8$ on the basis of chemical shift.

• 한국산학기술학회논문지
• /
• 제4권3호
• /
• pp.296-300
• /
• 2003

다성분 양이온 교환을 위한 평형과 동역학 데이터는 질량 작용 법칙과 표면 착화 모델을 이용하여 수행 및 평가하였다. 양이온 흡착의 평형과 칼럼 실험은 양이온 교환 합성 수지 IRN 77로 H/sup +/, Li/sup +/, Na/sup +/, NH₄/sup +/, Mg²/sup +/ 이용하여 2, 3, 4, 5 성분 양이온 교환을 수행하였다. 질량 작용 법칙과 표면 착화 모델은 이온 선택도와 경쟁적 양이온 교환을 조사하기 위하여 데이터에 대해 시험하였다. 표면 착화 모델은 질량 작용 모델보다 평형과 동역학 실험 데이터를 정확히 예측하였다.

• Korean Chemical Engineering Research
• /
• 제44권4호
• /
• pp.340-344
• /
• 2006

폴리스티렌을 acetyl sulfate 시약을 사용하여 술폰화시킨 후 다공성 양이온교환 막으로 제조하였다. 제조된 막의 특성을 분석한 결과 다공성의 형태를 가졌음을 확인할 수 있었고, IR 분석결과 술폰산기의 도입을 확인할 수 있었다. 전체적으로 반응물 중 황산의 양이 증가할수록 이온교환능력이 증가하는 경향을 확인할 수 있었고, 전기투석 공정에 적용가능성을 판단한 결과 양이온에 대한 선택성과 음이온에 대한 배제성을 간접적으로 확인할 수 있었다.