Pseudomonas otitidis WL-13, which has a high capacity to decolorize triphenylmethane dyes, was isolated from activated sludge obtained from a wastewater treatment plant of a dyeing industry. This strain exhibited a re...Pseudomonas otitidis WL-13, which has a high capacity to decolorize triphenylmethane dyes, was isolated from activated sludge obtained from a wastewater treatment plant of a dyeing industry. This strain exhibited a remarkable color-removal capability when tested against several triphenylmethane dyes under both shaking and static conditions at high concentrations of dyes. More than 95% of Malachite Green and Brilliant Green was removed within 12 h at 500 μmol/L dye concentration under shaking conditions. Crystal Violet lost about 13% of its color under the same conditions tested. The rate of decolorization increased when the M9 medium was supplemented with yeast extract. The optimum pH and temperature for color removal were 7-9 and 35-40℃, respectively. The observed changes in the visible spectra and the inspection of bacterial growth indicated the color-removal by the adsorption of dye to the cells during incubation with strains.展开更多
In pH 4.5-7.0 Britton-Robinson buffer solution,furosemide (FUR) reacted with Pd (II) to form a 1:1 anionic chelate.This chelate could further react with such basic triphenylmethane dyes (BTPMD) as ethyl violet (EV),cr...In pH 4.5-7.0 Britton-Robinson buffer solution,furosemide (FUR) reacted with Pd (II) to form a 1:1 anionic chelate.This chelate could further react with such basic triphenylmethane dyes (BTPMD) as ethyl violet (EV),crystal violet (CV),methyl violet (MV),methyl green (MeG) and brilliant green (BG) to form 1:1 ion-association complexes.This not only resulted in the change of absorption spectra,but also led to the significant enhancement of resonance Rayleigh scattering (RRS),second-order scattering (SOS) and frequency doubling scattering (FDS).The maximum RRS wavelengths were located at 324 nm for the EV,CV and MV system,and 340 nm for the BG and MeG system.The maximum SOS wavelengths were located at 550 nm for the EV,CV,BG and MeG system,and 530 nm for the MV system.The maximum scattering peaks of all the systems were at 392 nm for FDS.The enhanced RRS,SOS and FDS intensities were directly proportional to the concentration of FUR.The detection limits for the different dye systems were 0.3-4.9 ng mL-1 for the RRS method,3.2-33.1 ng mL-1 for the SOS method and 9.0-85.7 ng mL-1 for the FDS method.These methods could be used for the determination of trace amounts of FUR.The effects of the formation of ternary ion-association complexes on the spectral characteristics and intensities of absorption,RRS,SOS and FDS have been investigated.The optimum conditions of these reactions,the influencing factors and the analytical properties have been tested.The influences of coexisting substances were tested by RRS method and the results showed that this method exhibited a high sensitivity.Based on the aforementioned research,the highly sensitive,simple and rapid methods for the determination of trace amounts of FUR by resonance light scattering technique have been established,which could be applied to the determination of FUR in tablet,injection,human serum and urine samples.The composition and structure of the ternary ion-association complex and the reaction mechanism were discussed.展开更多
This paper described a novel method for the preconcentration of Pb（II） using microcrystalline triphenylmethane loaded with quinolin-8-olate prior to the determination by flame atomic absorption spectrometry. Pb（II...This paper described a novel method for the preconcentration of Pb（II） using microcrystalline triphenylmethane loaded with quinolin-8-olate prior to the determination by flame atomic absorption spectrometry. Pb（II） could be enriched by controlling appropriate condition. The preconcentration factor could reach to 200 and the detection limit of Pb（II） was 0.074 μg/L. The recovery was in a range of 93.5-103% with relative standard deviation of 1.0-2.2%. The proposed method had been successfully applied to the determination of trace Pb（U） in various water samples with satisfactory result.展开更多
The paper describes a novel method for copper preconcentration using microcrystalline triphenylmethane loaded with malachite green prior to the determination by the flame atomic absorption spectrometry （FAAS）. Under...The paper describes a novel method for copper preconcentration using microcrystalline triphenylmethane loaded with malachite green prior to the determination by the flame atomic absorption spectrometry （FAAS）. Under the optimum conditions, Cu（Ⅱ） can be totally adsorbed on the surface of microcrystalline triphenylmethane, and completely separated from Pb（Ⅱ）, Cd（Ⅱ）, Co（Ⅱ）, Cr（Ⅲ）, Ni（Ⅱ）, Mn（Ⅱ）, Fe（Ⅲ） and Al（Ⅲ） by controlling acidity. The preconcentration factor of this proposed method is 200. The recovery is in a range of 97.5%-105%. The relative standard deviation （RSD） is not beyond 3.0%. The proposed method has been successfully applied to the determination of trace copper in various water samples with satisfactory results.展开更多
Herein,we found that anthraquinone(AQ)acted as a catalyst for the rapid and effective removal of triphenylmethane dye containing tertiary amino group(TDAG).Results showed that AQ had an enhanced catalytic reactivity t...Herein,we found that anthraquinone(AQ)acted as a catalyst for the rapid and effective removal of triphenylmethane dye containing tertiary amino group(TDAG).Results showed that AQ had an enhanced catalytic reactivity towards the removal of TDAG compared to hydro-quinone,which was further proved and explained using density functional theory(DFT)calculations.AQs could achieve a TDAG removal efficiency and rate of approximately 100%and 0.3583 min^(−1),respectively,within 20 min.Quenching experiments and electron paramagnetic resonance(EPR)tests indicated that the superoxide radical(O_(2)^(•−))generated through the catalytic reduction of an oxygen molecule(O_(2))by AQ contributed to the effective removal of the TDAG.In addition,itwas found that the electrophilic attack of the O_(2)^(•−)radical on the TDAG was the driving force for the dye degradation process.Decreasing the pH led to protonation of the substituted group of AG,which resulted in formation of an electron deficient center in the TDAGmolecule(TDAG-EDC+)through delocalization of the π electron.Therefore,the possibility of the electrophilic attack for the dye by the negative O_(2)^(•-)radical was significantly enhanced.This study revealed that the H+and the O_(2)^(•−)generated by the catalytic reduction of O_(2) have synergistic effects that led to a significant increase in the dye removal rate and efficiency,which were higher than those obtained through persulfate oxidation.展开更多
In recent years, the ability of microorganisms to decolorize textile wastewater has received great attention due to the environmental persistence and toxicity of these pollutants. In this paper biological decolorizati...In recent years, the ability of microorganisms to decolorize textile wastewater has received great attention due to the environmental persistence and toxicity of these pollutants. In this paper biological decolorization of triphenylmethane dye, C.I. Basic Green 4 (BG 4), by Chlorella species was investigated. The effect of operational parameters (temperature, pH, initial dye concentration and algal concentration) on decolorization efficiency was examined. Results indicated that the desired initial pH was 9. The stability and efficiency of the algae in long-term repetitive operations were also examined. Michaelis–Menten kinetics was employed to describe the apparent correlation between the decolorization rate and dye concentration. The optimal kinetic parameters, νmax (specific decolorization rate) and Km (maximum specific decolorization rate) were 4.6 mg dye g cell-1 h-1 and 151.0 mg L-1, respectively.展开更多
A systematic study of the synthesis of C.I.Acid Blue 9 leuco compound in water is reported.The kinetic analysis of experimental data for the condensation reaction between 2-formylbenzenesulfonic acid sodium and N-ethy...A systematic study of the synthesis of C.I.Acid Blue 9 leuco compound in water is reported.The kinetic analysis of experimental data for the condensation reaction between 2-formylbenzenesulfonic acid sodium and N-ethyl-N-(3'-sulfonic acid benzyl) aniline obtained at four different temperatures ranging between 85 and 100°C is discussed.It is shown that the reaction followed second-order rate kinetics.The overall rate constant(k) increased with the increase of temperature.On the basis of the value of k,activation energy(E_a) of the reaction was evaluated.Importantly,it is found that reactant concentration has great effect on the formation of C.I.Acid Blue 9 leuco compound,implying that it is not enough to improve the conversion of N-ethyl-N-(3'-sulfonic acid benzyl) aniline by only prolonging reaction time in the late period of the reaction.展开更多
In a thin HCl medium,RRS intensities of an alone CS or acidic triphenylmethane dye (TPMD) are very week. However,when TPMD reacts with a CS to form an ion-associate,the RRS intensity is enhanced greatly and a new RRS ...In a thin HCl medium,RRS intensities of an alone CS or acidic triphenylmethane dye (TPMD) are very week. However,when TPMD reacts with a CS to form an ion-associate,the RRS intensity is enhanced greatly and a new RRS spectrum appears. The spectral characteristics of the RRS for the ion-associates and the optimum conditions for the reactions are investigated. The intensity of RRS is directly proportional to the mass concentration of CS in the range of 0—3.5 or 0—5.0 μg/mL. The method has a high sensitivity for the determination of CS,their detection limits are between 3.1 and 9.8 ng/mL depending on the different CS. In this case,most metal and non-metal ions do not interfere,so that the method has a good selectivity. Therefore,a sensitive,selective,simple and rapid method for the determination of CS by RRS is developed. [WT5HZ]展开更多
基金supported by the Dong-A University Research Fund in 2007
文摘Pseudomonas otitidis WL-13, which has a high capacity to decolorize triphenylmethane dyes, was isolated from activated sludge obtained from a wastewater treatment plant of a dyeing industry. This strain exhibited a remarkable color-removal capability when tested against several triphenylmethane dyes under both shaking and static conditions at high concentrations of dyes. More than 95% of Malachite Green and Brilliant Green was removed within 12 h at 500 μmol/L dye concentration under shaking conditions. Crystal Violet lost about 13% of its color under the same conditions tested. The rate of decolorization increased when the M9 medium was supplemented with yeast extract. The optimum pH and temperature for color removal were 7-9 and 35-40℃, respectively. The observed changes in the visible spectra and the inspection of bacterial growth indicated the color-removal by the adsorption of dye to the cells during incubation with strains.
文摘In pH 4.5-7.0 Britton-Robinson buffer solution,furosemide (FUR) reacted with Pd (II) to form a 1:1 anionic chelate.This chelate could further react with such basic triphenylmethane dyes (BTPMD) as ethyl violet (EV),crystal violet (CV),methyl violet (MV),methyl green (MeG) and brilliant green (BG) to form 1:1 ion-association complexes.This not only resulted in the change of absorption spectra,but also led to the significant enhancement of resonance Rayleigh scattering (RRS),second-order scattering (SOS) and frequency doubling scattering (FDS).The maximum RRS wavelengths were located at 324 nm for the EV,CV and MV system,and 340 nm for the BG and MeG system.The maximum SOS wavelengths were located at 550 nm for the EV,CV,BG and MeG system,and 530 nm for the MV system.The maximum scattering peaks of all the systems were at 392 nm for FDS.The enhanced RRS,SOS and FDS intensities were directly proportional to the concentration of FUR.The detection limits for the different dye systems were 0.3-4.9 ng mL-1 for the RRS method,3.2-33.1 ng mL-1 for the SOS method and 9.0-85.7 ng mL-1 for the FDS method.These methods could be used for the determination of trace amounts of FUR.The effects of the formation of ternary ion-association complexes on the spectral characteristics and intensities of absorption,RRS,SOS and FDS have been investigated.The optimum conditions of these reactions,the influencing factors and the analytical properties have been tested.The influences of coexisting substances were tested by RRS method and the results showed that this method exhibited a high sensitivity.Based on the aforementioned research,the highly sensitive,simple and rapid methods for the determination of trace amounts of FUR by resonance light scattering technique have been established,which could be applied to the determination of FUR in tablet,injection,human serum and urine samples.The composition and structure of the ternary ion-association complex and the reaction mechanism were discussed.
文摘This paper described a novel method for the preconcentration of Pb（II） using microcrystalline triphenylmethane loaded with quinolin-8-olate prior to the determination by flame atomic absorption spectrometry. Pb（II） could be enriched by controlling appropriate condition. The preconcentration factor could reach to 200 and the detection limit of Pb（II） was 0.074 μg/L. The recovery was in a range of 93.5-103% with relative standard deviation of 1.0-2.2%. The proposed method had been successfully applied to the determination of trace Pb（U） in various water samples with satisfactory result.
基金Project supported by the Natural Science Foundation of Henan Province （No. 0511020500） and Innovation Project Foundation of University in Henan Province （No. 2001-513）.
文摘The paper describes a novel method for copper preconcentration using microcrystalline triphenylmethane loaded with malachite green prior to the determination by the flame atomic absorption spectrometry （FAAS）. Under the optimum conditions, Cu（Ⅱ） can be totally adsorbed on the surface of microcrystalline triphenylmethane, and completely separated from Pb（Ⅱ）, Cd（Ⅱ）, Co（Ⅱ）, Cr（Ⅲ）, Ni（Ⅱ）, Mn（Ⅱ）, Fe（Ⅲ） and Al（Ⅲ） by controlling acidity. The preconcentration factor of this proposed method is 200. The recovery is in a range of 97.5%-105%. The relative standard deviation （RSD） is not beyond 3.0%. The proposed method has been successfully applied to the determination of trace copper in various water samples with satisfactory results.
基金supported by the Strategic Research and Development Program of Shaanxi Province (No. 2019ZDLSF06-02)the Special Project for Serving Local S&T Development of Education Department, Shaanxi Province (No. 21JC022)。
文摘Herein,we found that anthraquinone(AQ)acted as a catalyst for the rapid and effective removal of triphenylmethane dye containing tertiary amino group(TDAG).Results showed that AQ had an enhanced catalytic reactivity towards the removal of TDAG compared to hydro-quinone,which was further proved and explained using density functional theory(DFT)calculations.AQs could achieve a TDAG removal efficiency and rate of approximately 100%and 0.3583 min^(−1),respectively,within 20 min.Quenching experiments and electron paramagnetic resonance(EPR)tests indicated that the superoxide radical(O_(2)^(•−))generated through the catalytic reduction of an oxygen molecule(O_(2))by AQ contributed to the effective removal of the TDAG.In addition,itwas found that the electrophilic attack of the O_(2)^(•−)radical on the TDAG was the driving force for the dye degradation process.Decreasing the pH led to protonation of the substituted group of AG,which resulted in formation of an electron deficient center in the TDAGmolecule(TDAG-EDC+)through delocalization of the π electron.Therefore,the possibility of the electrophilic attack for the dye by the negative O_(2)^(•-)radical was significantly enhanced.This study revealed that the H+and the O_(2)^(•−)generated by the catalytic reduction of O_(2) have synergistic effects that led to a significant increase in the dye removal rate and efficiency,which were higher than those obtained through persulfate oxidation.
基金Financially supported by the University of Tabriz, Iran
文摘In recent years, the ability of microorganisms to decolorize textile wastewater has received great attention due to the environmental persistence and toxicity of these pollutants. In this paper biological decolorization of triphenylmethane dye, C.I. Basic Green 4 (BG 4), by Chlorella species was investigated. The effect of operational parameters (temperature, pH, initial dye concentration and algal concentration) on decolorization efficiency was examined. Results indicated that the desired initial pH was 9. The stability and efficiency of the algae in long-term repetitive operations were also examined. Michaelis–Menten kinetics was employed to describe the apparent correlation between the decolorization rate and dye concentration. The optimal kinetic parameters, νmax (specific decolorization rate) and Km (maximum specific decolorization rate) were 4.6 mg dye g cell-1 h-1 and 151.0 mg L-1, respectively.
基金Supported by the National Natural Science Foundation of China(U1608223,21576044,21421005,21536002)the Dalian University of Technology Innovation Team(DUT2016TB12)
文摘A systematic study of the synthesis of C.I.Acid Blue 9 leuco compound in water is reported.The kinetic analysis of experimental data for the condensation reaction between 2-formylbenzenesulfonic acid sodium and N-ethyl-N-(3'-sulfonic acid benzyl) aniline obtained at four different temperatures ranging between 85 and 100°C is discussed.It is shown that the reaction followed second-order rate kinetics.The overall rate constant(k) increased with the increase of temperature.On the basis of the value of k,activation energy(E_a) of the reaction was evaluated.Importantly,it is found that reactant concentration has great effect on the formation of C.I.Acid Blue 9 leuco compound,implying that it is not enough to improve the conversion of N-ethyl-N-(3'-sulfonic acid benzyl) aniline by only prolonging reaction time in the late period of the reaction.
文摘In a thin HCl medium,RRS intensities of an alone CS or acidic triphenylmethane dye (TPMD) are very week. However,when TPMD reacts with a CS to form an ion-associate,the RRS intensity is enhanced greatly and a new RRS spectrum appears. The spectral characteristics of the RRS for the ion-associates and the optimum conditions for the reactions are investigated. The intensity of RRS is directly proportional to the mass concentration of CS in the range of 0—3.5 or 0—5.0 μg/mL. The method has a high sensitivity for the determination of CS,their detection limits are between 3.1 and 9.8 ng/mL depending on the different CS. In this case,most metal and non-metal ions do not interfere,so that the method has a good selectivity. Therefore,a sensitive,selective,simple and rapid method for the determination of CS by RRS is developed. [WT5HZ]
