• 대한화학회지
• /
• 제38권9호
• /
• pp.660-666
• /
• 1994

이웃하는 란탄족 원소의 분리에서 온도와 흐름속도의 영향을 치환크로마토그래피로 연구하였다. 일렬로 연결된 두 컬럼에 Amberlite 120 양이온 교환수지를 채워서 충전용과 분리용으로 나누어 사용하였다. 보유이온은 $H^+$을, 흐름용액은 0.012M과 0.015M의 EDTA 용액을 사용하였다. 실험중에는 관의 온도를 90$^{\circ}C$로 유지하였으며 이온교환수지 관 속에 생기는 기포를 줄이기 위해 일정한 압력을 걸었다. 용출액은 ICP-AES로 직접 분석하였다. 이 실험에서 란탄족 원소쌍 La: Ce, Ce :Pr, Pr: Nd에 대한 분리인자는 각각 4.6, 2.8, 1.9이었으며 이것은 25$^{\circ}C$에서 이론적으로 얻은 것보다 큰 값이다. 흐름속도를 2.5 ml/min에서 1.5 ml/min로 줄이면 이론단해당높이(HETP)도 1.60 cm에서 0.88 cm로 줄었다. 따라서 용리액의 흐름속도를 줄이고 온도를 높이므로써 분리효율을 증가시킬 수 있었다. 이 실험에서 99.9% 이상의 순수 란탄족 원소에 대한 회수율은 49∼77%이었다.

• 대한화학회지
• /
• 제43권2호
• /
• pp.161-166
• /
• 1999

Ionophore ETH4120의 이온담체작용에 의한 란탄족원소이온의 액체/액체계면에서의 상전이를 순환전압전류법(cyclic voltammetry)과 순환전류주사 대시간전위차법(Chronopotentiometry with cyclic linear current scanning; CPCLCS)으로 고찰하였다. 수용액 중의 란탄족원소이온농도가 유기용액중의 착화제 농도보다 훨씬 높을 때 순환전압전류법과 CPCLCS 곡선에서 하나의 양극전류(수용액상에서 유기상으로 전이)파와 두개의 음극전류(유기상에서 수용액상으로 전이)파가 관찰되었다. 양극전류파는 1:1(금속:착화제) 착물형성과 관계되는 봉우리이고, 두 음극전류파는 각각 1:2와 1:3의 연속적인 착물형성과 관계된 파이다. 그러나 1:1 착물의 양극전류파와 대응하는 1:1 착물의 음극파와, 1:2 착물과 1:3 착물의 음극전류파에 대응되는 양극전류파는 나타나지 않았다. 이와 관련되는 이온 상전이 메카니즘을 검토하였다.

• 대한화학회지
• /
• 제38권1호
• /
• pp.50-54
• /
• 1994

흐름주입법에 의하여 분광광도법으로 몇 가지 가벼운 란탄족 원소를 정량하였다. Chromeazurol S는 양이온 계면활성제인 DTAB존재하에서 란탄족 이온과 착물을 형성한다. Tris 완충용액(pH 10.5)에서 이 착물의 최대흡수파장은 650 nm 에서 655 nm범위이고 몰흡광계수는 약 $1.8{\times}10^5\;L mol^{-1}cm^{-1}$였다. FIA에 의한 Nd(III), Eu(III) 및 Sm(III)의 검정곡선은 0.1 ~ 0.6 ppm에서 직선관계를 보였고, 이 검정곡선의 상관계수(${\gamma}$)는 0.9993이였다. 검출한계(S/N)는 Nd(III)과 Eu(III)에 대하여는 10 ppb이고, Sm(III)에 대하여는 20 ppb였다. 상대표준편차는 시료 0.4 ppm에 대하여 약 ${\pm}$1.2%이고, 시료의 분석 속도는 약 $50hr^{-1}$였다.

• Bulletin of the Korean Chemical Society
• /
• 제28권8호
• /
• pp.1249-1255
• /
• 2007

We have investigated the photophysical properties of dansyl-N-methylaminobenzoic acid (DABAH) as a ligand and its lanthanide (Ln3+)-cored complexes (Ln3+-(DABA)3(terpy)) in order to determine the main energy transfer pathway for sensitized near infrared emission of Ln3+ ions (Ln3+ = Nd3+ and Er3+) in Ln3+- (DABA)3(terpy). The fluorescence spectrum of DABAH shows a large Stokes shift with increasing solvent polarity. This large Stokes shift might be due to the formation of a twisted intramolecular charge transfer (TICT) state, as demonstrated by the large dipole moment in the excited state. It is in good agreement with the result that the phosphorescence even in the Gd3+-cored complex based on the DABAH ligand was not observed, maybe due to the highly forbidden character of the S1 → T1 transition in the DABAH ligand. A short decay component (ca. 1 ns) was observed in Er3+-(DABA)3(terpy) whereas the fluorescence lifetimes of DABAH and its Gd3+-(DABA)3(terpy) are observed about ~10 ns. The short component could be originated from the energy transfer process between the ligand and the Ln3+ ion. Based on the fluorescence of DABAH its Ln3+- (DABA)3(terpy), the sensitization of Ln3+ luminescence in the Ln3+-(DABA)3(terpy) takes place by the energy transfer via the TICT state of DABAH in the excited singlet state rather than via the excited triplet state.

• Bulletin of the Korean Chemical Society
• /
• 제27권11호
• /
• pp.1839-1843
• /
• 2006

Hydrothermal reactions of $Ln(NO_3)_3{\cdot}5H_2O $ (Ln = Eu (1), Sm (2), Ho (3), Dy (4)) with 3,5-pyridinedicarboxylic acid (3,5-pdcH2) in the presence of 4,4'-bipyridine led to the formation of the 3-D Ln(III)-coordination polymers with a formula unit of $[Ln_2(3,5-pdc)_2(C_2O_4)(H_2O)_4]{\cdot}2H_2O$. These polymers contain a bridging oxalate ligand ($C_2O_4\;^2$). On the basis of GCMS study of the mother liquor remaining after the reaction, we proposed that the $C_2O_4\;^2$ formation proceeds in three steps: (1) Ln(III)-mediated decarboxylation of $3,5-pdcH_2$ to give $CO_2$, (2) the reduction of $CO_2$ to $CO_2\;^{\cdot}$ by the Ln(II) species, and (3) the reductive coupling of the two $CO_2\;^{\cdot}$ radicals to the oxalate ($C_2O_4\;^2$) ion. All polymers were structurally characterized by X-ray diffraction.

• 대한방사성의약품학회지
• /
• 제7권2호
• /
• pp.69-77
• /
• 2021

No-carrier-added holmium-166 (n.c.a ¹⁶⁶Ho) separation is performed based on the results of separation conditions using stable isotopes dysprosium (Dy) and holmium (Ho) to minimize radioactive waste from separation optimization procedures. Successful separation of two adjacent lanthanides was achieved by cation-exchange chromatography using a sulfonated resin in the H+ form (BP-800) and α-hydroxyisobutyric acid (α-HIBA) as eluent. For the identification process after separation of stable isotopes, the use of chromogenic reagents alternatively enables on-line detection because the lanthanides are hardly absorb light in the UV-vis region or exhibit radioactivity. Four different chromogenic reagents were pre-tested to evaluate suitable coloring reagents, of which 4-(2-Pyridylazo)resorcinol is the most recommendable considering the sensitivity and specificity for lanthanides. Lanthanide radioisotopes (RI) were monitored for separation with an RI detector using a lab-made separation LC system. Under the proper separation conditions, the n.c.a ¹⁶⁶Ho was effectively obtained from a large amount of 100 mg dysprosium target within 2 hrs.

• 한국환경과학회지
• /
• 제20권4호
• /
• pp.511-517
• /
• 2011

Ti-SBA-15 catalysts doped with samarium ion were synthesized using conventional hydrothermal method. The physical properties of Sm/Ti-SBA-15 catalysts have been characterized by XRD, FT-IR, DRS and PL. In addition, we have also examined the activity of these materials on the photocatalytic decomposition of methylene blue. The Sm/ Ti-SBA-15 was shown to have the mesoporous structure regardless of Sm ion doping. With doping amount of 1% lanthanide ion, the pore size and pore volume of Sm(Er, Cs)/Ti-SBA-15 decreased and the surface area increased. For the purpose of vibration characteristics on the Ti-SBA-15 and Sm/Ti-SBA-15 photocatalysts, the IR absorption at 960 $cm^{-1}$ commonly accepted the characteristic vibration of Ti-O-Si bond. 1% of Sm/Ti-SBA-15 had the highest photocatalytic activity on the decomposition of methylene blue but the catalysts doped with Er ions had lower activity in comparison with pure Ti-SBA-15 catalyst.

• 대한화학회지
• /
• 제36권2호
• /
• pp.205-211
• /
• 1992

아세트아미드(AA)의 CO기와 희토류 금속이온(Ln(II))을 포함하는 몇 가지 lanthanide shift reagent(LSR) 사이의 상호작용을 이해하기 위하여 AA의 $2{\nu}_{C=0}$ + amide III 조합띠를 $15^{\circ}$ ${\sim} 45^{\circ}C$에서 조사하였다. 묽은 $CCl_4$ 용액속에서 하나의 AA가 사용된 LSR에 배위되어 1 : 1 AA-LSR 복합체를 이루며, Ln(Ⅲ)이온에 대한 AA의 배위 위치는 카르보닐의 산소임을 알았다. 온도 및 농도에 따른 이 조합띠의 변화로부터 Ln(III)${\cdot}$O=C 결합에 대한 여러가지 열역학적 함수들을 구했다. Eu$(dpm)_3$, Yb$(dpm)_3$ 및 Pr$(dpm)_3$에 대한 AA의 결합의 세기를 나타내는 ${\Delta}H^{\circ}$는 각각 -39.1, -28.4 및 -25.5kJ/mol이다. 이들 값을 비교해보면 AA 분자가 배위될 때 중심금속이온의 ionic potential 효과보다는 이미 배위되어 있는 커다란 dpm 분자에 의한 입체장애효과가 더 큼을 알 수 있다.

• Bulletin of the Korean Chemical Society
• /
• 제24권1호
• /
• pp.49-54
• /
• 2003

TiO₂nanoparticles were synthesized using the metallorganic chemical vapor deposition process. Particles with and without metal ion dopants were obtained. X-ray photoelectron and energy dispersive X-ray spectroscopic measurements confirmed the stoichiometry of the TiO₂nanoparticles. X-ray diffraction patterns showed a polycrystalline anatase structure of TiO₂. Transmission electron microscopy revealed that these particles are of nanoscale dimensions. Exact particle size and size distribution analyses were carried out by dynamic light scattering. The average particle size was determined to be 22 nm. The nanosize particles provided large surface area for photocatalysis and a large number of free surface-charge carriers, which are crucial for the enhancement of photocatalytic activity. To improve the photocatalytic activity, metal ions, including transition metal ions $(Pd^{2+},\;Pt^{4+},\;Fe^{3+})$ and lanthanide ion $(Nd^{3+})$ were added to pure TiO₂nanoparticles. The effects of dopants on photocatalytic kinetics were investigated by the degradation of 2-chlorophenol under an ultraviolet light source. The results showed that the TiO₂nanoparticles with the metal ion dopants have higher photocatalytic activity than undoped TiO₂. The $Nd^{3+}$ ion of these dopant metal ions showed the highest catalytic activity. The difference in the photocatalytic activity with different dopants is related to the different ionic radii of the dopants.

• 한국유가공학회:학술대회논문집
• /
• 한국유가공기술과학회 1997년도 춘계 제44회 유가공 심포지움
• /
• pp.23-34
• /
• 1997

Calcium-stimulated ATPase ($Ca^{2+}$-ATPase) which has optimal pH value at 7.0 was found in the membrane fraction of human milk, and its enzymatic properties were studied. The purified $Ca^{2+}$-ATPase required 0.45 mM Ca ion for maximal activity. Among the nucleosides, $Ca^{2+}$-ATPase showed a higher substrate specificity to ATP and UTP than to CTP and GTP. $Ca^{2+}$-ATPase had apparent Km value of 0.065, and V max of 7.63 mol ATP hydrolyzed/mg pro-tein per min, respectively. $Ca^{2+}$-ATPase was potently inhibited by lanthanide, vanadate, and p-chloromercuribenzoate, and inactivated by EDTA, and CDTA and EGTA, but were unaffected by N-ethylmaleimide, $NaN_3$, ouabain, or oligomycin, and was completely inactivated by heating at $60^{\circ}C$ for 10 min. This enzyme activity was concentrated in the membrane fraction of the cream and skim milk membrane, but not founded in bovine milk.