• Journal of Environmental Health Sciences
• /
• v.34 no.3
• /
• pp.226-232
• /
• 2008

A feasibility study for the application of the photoelectrocatalytic decolorization of Rhodamine B (RhB) was performed in a photoelectrochemical reactor with immobilized $TiO_2$ particle. The effects of operating conditions, such as current, electrolyte and pH were evaluated. The experimental results showed that optimum $TiO_2$ dosage and current in the photoelectrocatalytic process were 83.3 g/l and 0.5 A, respectively. It was found that the RhB could be degraded more efficiently by this photoelectrocatalytic process than the sum of the two individual oxidation processes (photocatalytic and electrolytic process). The addition of NaCl increased the initial decolorization rate and reduced reaction time. The optimum dosage of NaCl was 0.15 g/l. The decolorization rate of the photoelectrocatalytic process increased sharply with a decrease in pH value. However when the NaCl was added, the pH effect was not high.

• Bulletin of the Korean Chemical Society
• /
• v.34 no.1
• /
• pp.159-163
• /
• 2013

A new Rhodamine B hydrazide hydrazone 1 has been synthesized and investigated as a colorimetric and fluorescent "off-on" sensor for the recognition of $Cu^{2+}$ in $CH_3CN/H_2O$ (1:1, v/v, HEPES 10 mM, pH = 7.0) solution. Sensor 1 displayed highly selective, sensitive and rapid recognition behavior toward $Cu^{2+}$ among a range of biologically and environmentally important metal ions. Sensor 1 bind $Cu^{2+}$ via a 1:1 stoichiometry with an association constant of $1.92{\times}10^6\;M^{-1}$, and the detection limit is evaluated to be $7.96{\times}10^{-8}\;M$. The $Cu^{2+}$ recognition event is reversible and is barely interfered by other coexisting metal ions.

• Bulletin of the Korean Chemical Society
• /
• v.34 no.2
• /
• pp.389-393
• /
• 2013

A rhodamine B-based fluorescent probe for nitrite ion ($NO{_2}^-$) has been designed, synthesized, characterized and its properties for recognition of $NO{_2}^-$ were studied. Nearly non fluorescent probe upon reaction with nitrite ion significantly triggered the fluorescence. Fluorescence response is based on ring opening of the spirolactam of rhodamine B phenyl hydrazide showing maximum absorbance at 552 nm and maximum emission at 584 nm. Probe 3 exhibited high sensitivity and extreme selectivity for nitrite ion over other common ions and oxidants ($Cl^-$, $ClO^-$, $ClO{_2}^-$, $ClO{_3}^-$, $ClO{_4}^-$, $SO{_4}^{2-}$, $SiO{_3}^{2-}$, $NO{_3}^{2-}$, $CO{_3}^{2-}$) examined in methanol water (1:1, v/v) at pH 7.0. The probe might be a new efficient tool for detection of nitrite ion in natural water and biological system.

• Korean Journal of Food Science and Technology
• /
• v.40 no.4
• /
• pp.375-381
• /
• 2008

This study developed the simultaneous analysis method for efficient safety controls of import food of Orange II, Rhodamine B, Para Red, and Sudan dye I-IV among disapproved coloring agents that use is prohibited in foods. The analysis method was developed according to the sample pre-treatment and HPLC conditions, and a documentary survey was used to establish the detection limit of the method, followed by effectiveness verification and recovery percentage examinations. Recovery percentage examination for 26 products resulted Orange II displayed recovery percentage of 96.46-121.26%, Rhodamine B displayed recovery percentage of 70.86-106.53%, Para Red displayed recovery percentage of 97.00-116.86%, Sudan I displayed recovery percentage of 92.93-112.44%, Sudan II displayed recovery percentage of 96.63-115.10%, Sudan III displayed recovery percentage of 92.21-114.73%, Sudan IV displayed recovery percentage of 93.22-122.91%. Correlation coefficient of gradient of this analysis method exhibited more than 0.999, RSD exhibited fewer than 2 as 0.8-1.39%, exactitude exhibited more than 90%. At this time, detection limit and fixed quantity limit decided by each 0.1 mg/L, 0.3 mg/L.

• Journal of Korean Society of Environmental Engineers
• /
• v.29 no.6
• /
• pp.662-669
• /
• 2007

The effect of advanced oxidation processes such as $O_3$, $UV/TiO_2$, $O_3/UV$ and $O_3/UV/TiO_2$ on decolorization and COD removal of Rhodamine B(RhB) wastewater were considered. The results showed that the higher the $O_3$ concentration was, the higher the decolorization observed and the optimum $TiO_2$ dosage was 0.4 g/L in $UV/TiO_2$ and $O_3/UV/TiO_2$ process. $O_3/UV$ process showed the higher initial decolorization rate constant and the shorter termination time for decolorization than those of the $O_3$ process. The decolorization rate constants in various systems followed the order of $O_3/UV/TiO_2>O_3/UV>O_3{\gg}UV/TiO_2$. The decolorization rate of the RhB solution in every processes was more rapid than the mineralization rate identified by COD removal. The latter took longer time for further oxidation. The COD removal rate constants in four systems followed the order of $O_3/UV/TiO_2>O_3/UV>UV/TiO_2{\geqq}O_3$. Among four processes, combined photocatalysis and ozonation$(O_3/UV/TiO_2)$ was the most prospective process for removing color and COD such as dye wastewater.

• Journal of Environmental Science International
• /
• v.17 no.5
• /
• pp.547-553
• /
• 2008

For the RhB removal from the wastewater, electrochemical method was adapted to this study. Three dimensionally stable anode (Pt, Ir and Ru) and graphite and Ru cathode were used. In order to identify decolorization, the effects of electrode, current density, electrolyte and air flow rate were investigated. The effects of electrode material, current, electrolyte concentration and air flow rate were investigated on the decolorization of RhB. Electro-Fenton's reaction was evaluated by added $Fe^{2+}$ and $H_2O_2$ generated by the graphite cathode. Performance for RhB decolorization of the four electrode systems lay in: Ru-graphite > Ru-Ru > Ir-graphite > Pt-graphite. A complete color removal was obtained for RhB (30 mg/L) at the end of 30 min of electrolysis under optimum operations of 2 g/L NaCl concentration and 2 A current. $Fe^{2+}$ addition increased initial reaction and decreased final RhB concentration. However the effect was not high.

• Rapid Communication in Photoscience
• /
• v.4 no.4
• /
• pp.88-90
• /
• 2015

The design and development of fluorescent chemosensors have recently been intensively explored for sensitive and specific detection of environmentally and biologically relevant metal ions in aqueous solution and living cells. Herein, we report the photophysical results of rhodamine B based fluorogenic and chromogenic receptor for selective copper detection in the complete organic or mixed aqueous-organic media at neutral pH under ambient condition. The ligand exhibited the remarkable increment in the fluorescence emission and UV-visible absorption signal intensities at 587 and 547 nm, respectively, on induction of copper ion while the ligand solution remain completely silent on addition of varieties of other metal ions.

• Journal of Biomedical Engineering Research
• /
• v.10 no.3
• /
• pp.237-242
• /
• 1989

The physical properties and drug release behaviours of polyethylene glycol grafted poly ${\gamma}$- benzyl L-glutamate (PEG- g- PBLG), polyethylene glycol crosslinked poly ${\gamma}$-benzyl L- glutamate(PEG-c-PBLG), and PBLG homopolymer are compared. PBLG containing PEG segements showed higher wettability and larger enlongation than PBLG homoplymer, but lower elastic modulus. The release rate of rhodamine is strongly influenced by the wettability of the polymer. Rhodamine is more rapidly released from PEG-c-PBLG membrane having a larger water contact angle than from other polymer having a lower water contact angle. The surfaces of PBLG derivative membranes are modified by substitution reaction using hydroxyalkylamine. The resulting polymer membranes showed hider wettability and swelling ratio than virgin membranes.

• Archives of Pharmacal Research
• /
• v.28 no.1
• /
• pp.93-99
• /
• 2005

Intracellular trafficking of transferrin-conjugated dimethyldioctadecyl-ammonium bromide liposome $(T_f-liposome)/DNA$ complexes in HeLa cells was studied using the double-labeled fluorescence technique and confocal microscopy. The size of the $T_f-liposome/DNA$ complex was about 367 nm in diameter and the zeta-potential of it at a 5:1 (w/w) ratio was almost neutral. The intracellular pathway of the $T_f-liposome/DNA$ complex, noted as green (FITC), red (rhodamine) or yellow (FITC + rhodamine) fluorescence, was elucidated from the plasma membrane to the endosome (or lysosome), and finally to the nucleus. The results of this study indicate that plasmid DNA enters into the nucleus not only as a free form but as an associated form complexed with $T_f-liposome$. More interestingly, the $T_f-liposome$ undergoes a nuclear location in the form of ordered structures. This could be a very useful piece of information in designing a safe and advanced gene delivery system.

• Proceedings of the Korean Environmental Sciences Society Conference
• /
• 2007.05a
• /
• pp.370-374
• /
• 2007

난분해성 유기물 처리에 적절한 불용성 전극을 선정하고 성능을 평가하기 위하여 1-3 성분계 전극을 이용하여 양이온 염료인 Rhodamine B (RhB)의 전기분해 처리에서 다음의 결론을 얻었다. 1) 반응 2분 후 RhB 농도를 고찰한 결과 RhB 농도감소는 Ru-Sn-Ti/Ti ${\fallingdotseq}$ Ru-Sn-Sb/Ti > Ir-Sn-Sb/Ti > Sn-Sb/Ti > Ru/Ti > Ir/Ti > Pt/Ti의 순서로 나타나 3성분계 > 2성분계 > 1성분계 전극의 순서로 나타났다. Ru를 사용한 전극이 Ir을 사용한 전극보다 1성분계와 3성분계 모두 성능이 우수한 것으로 나타났다. 기존 전극으로 가장 많이 사용되고 있는 Pt 전극의 성능은 가장 떨어지는 것으로 나타났다. 2) RhB 초기 농도감소 속도는 전극 간격이 좁은 것이 유리한 것으로 나타났으나 최종 농도는 비슷하였다. 전극 간격이 좁을수록 전력 면에서 유리한 것으로 나타났다. 면적이 큰 전극이 초기 반응이 빠르고 나타났고 최종농도도 약간 낮은 것으로 나타났으나 차이는 크지 않았다. 면적이 좁은 경우 반응면적이 적지만 전류밀도가 높기 때문에 성능의 차이는 크지 않으나 면적이 적은 전극의 경우 요구 전력량이 높기 때문에 적절한 크기의 전극이 필요한 것으로 사료되었다.