• Environmental Engineering Research
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• v.25 no.4
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• pp.529-535
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• 2020

The present study investigated the photodegradation of synthetic organic dye; violet-3B, without and with the addition of C-N-codoped TiO₂ catalyst using a visible halogen-lamp as a light source. The catalyst was synthesized by using a peroxo sol-gel method with free-organic solvent. The effects of initial dye concentration, catalyst dosage, and pH solution on the photodegradation of violet-3B were examined. The efficiency of the photodegradation process for violet-3B dye was higher at neutral to less acidic pH. The kinetics reaction rate of photodegradation of violet-3B dye with the addition of C-N-codoped TiO₂ followed pseudo-first order kinetics represented by the Langmuir-Hinshelwood model, and increasing the initial concentration of dyes decreased rate constants of photodegradation. Photodegradation of 5 mg L^-1 violet-3B dye achieved 96% color removal within 240 min of irradiation in the presence of C-N-codoped TiO₂ catalyst, and approximately 44% TOC was removed as a result of the mineralization.

• Analytical Science and Technology
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• v.15 no.5
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• pp.393-398
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• 2002

A method to determine simultaneously fluorene and anthracene in aqueous solution by synchronous fluorescence spectrometry has been studied. The emission characteristics and optimum wavelength interval (${\Delta}{\lambda}$) for synchronous spectra of fluorene and anthracene in aqueous solution were investigated. The optimum wavelength interval (${\Delta}{\lambda}$) was found to be 50 nm. The calibration curve for fluorene and anthracene in the synthetic mixture solution of both compounds was linear over the range from $5.0{\times}10^{-8}M$ to $1.0{\times}10^{-3}M$ and from $5.0{\times}10^{-8}M$ to $1.0{\times}10^{-3}M$ for fluorene and anthracene, respectively. The detection limit was $3.0{\times}10^{-9}M$ and $7.0{\times}10^{-9}M$, for fluorene and anthracene, respectively under the optimal wavelength interval.

• Analytical Science and Technology
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• v.23 no.5
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• pp.477-484
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• 2010

Personal care products are a diverse group of synthetic organic chemicals such as antimicrobial compounds, UV filters and organo-phosphate flame retardants and derived from individual usages of soaps, toothpaste and cosmetics. It has been detected in municipal sewage effluent and various environmental samples such as surface water, marine, soil, sediment and aquatic biota in many countries. The occurrence of personal care products in environmental samples could negatively impact the health of the ecosystem and humans, due to persistent, long-term chronic exposure of aquatic organisms. In this study, fifteen personal care products in aquatic environmental samples were determined by gas chromatography-mass spectrometry (GC-MS) with liquidliquid extraction (LLE). Method detection limits were in the range of $0.004\sim0.273\;{\mu}g/L$. Two compounds (TCEP, TCPP) were detected in surface waters and seven compounds (triclosan, 4-MBC, EHMC, BP-3, TCEP, TPP, TBEP) were detected in sewage treatment plants (STP) influents or effluents.

• Analytical Science and Technology
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• v.11 no.3
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• pp.213-221
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• 1998

The determination of inorganic anions by capillary zone electrophoresis is reported. A ten component synthetic mixture of anions of bromide, chloride, fluoride, nitrite, nitrate, sulfite, sulfate, perchlorate, chlorate and chlorite was separated by the capillary column and detected by indirect UV method. The running buffer contained 5 mM ammonium dichromate, 10 mM ammonium acetate, 20 mM diethylenetriamine, 10% methanol solution at pH 9.3. A potential of 15 kV at the cathode (reversed polarity) was utilized for the separation of inorganic anions. A complete separation of anions was achieved in less then 10 min and the applicabilities of the method for the analysis of real samples was demonstrated. We compare the concentration of anions in toluene inhaled humen's urine and in postmortem bloods obtained by capillary zone electrophoresis and ion chromatograph.

• Analytical Science and Technology
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• v.13 no.5
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• pp.573-583
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• 2000

Activated carbon fibers (ACFs) were prepared from various precursors of plantic, synthetic, and mixed fabrics of viscous rayon and cotton. Their adsorption performances of phenol and methylene blue in aqueous phase were evaluated through their adsorption isotherms, adsorption rates and breakthrough curves. The two adsorbates showed type I adsorption isotherm on ACFs. Adsorption rates to ACFs were 100 fold faster than to GAC. The effective diffusion coefficients of the adsorbates in ACFs were twenty fold greater than in GAC. The ACFs removed completely ten organic pollutants from a prepared water specimens through the 2nd column of a natural filtration method where 50 L of the water samples were treated.

• Analytical Science and Technology
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• v.5 no.2
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• pp.177-184
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• 1992

A preparation method and response characteristics of a glucose sensor which consisted of pH-ISFET and glucose oxidase-immobilized membrane were investigated. The pH-ISFET glucose sensor was fabricated by immbilizing bovine serum albumin and glucose oxidase with glutaraldehyde on gate of the pH-ISFET. Effects of pH and concentration of working buffer and enzyme load on the pontentiometric response of the pH-ISFET glucose sensor were examined. Response characteristics for the determination of glucose in synthetic physiological saline solution(pH 7.4) were as follows. That is the concentration range of linear response, slope of linear response(sensitivity), and response time were $1.0{\times}10^{-4}{\sim}6.0{\times}10^{-3}M $, 4.1 mV/decade, and 12~15 min., respectively.

• Analytical Science and Technology
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• v.11 no.6
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• pp.452-459
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• 1998

Crosslinked chitin was prepared from epichlorohydrin and chitin which was isolated from waste marin source. The crosslinked chitosan were prepared by the deacetylation of the crosslinked chitin with a strong base. 2,2'-Iminodibenzoic acid-crosslinked chitosan was prepared by reacting 2,2'-Iminodibenzoic acid salt with crosslinked chitosan-Cl which was obtained by chlorination of crosslinked chitosan. The adsorptivity of Pb(II), Cu(II), Cd(II) was studied as a synthetic adsorbent. Experimental results for the adsorption and the recovery characteristics showed that the more pH increase, the more amount of adsorbed metal ion increase. Optimum adsorption time was 1 hr, and adsorption capacity was increased in order of $Cu^{2+}$<$Cd^{2+}$<$Pb^{2+}$, and recovery capacity was increased in order of $Cd^{2+}$<$Cu^{2+}$<$Pb^{2+}$.

• Analytical Science and Technology
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• v.13 no.1
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• pp.89-95
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• 2000

Three grades of activated carbon fibers (ACFs) were prepared from various precursors of plantic, synthetic, and mixed fabrics of viscose rayon and cotton. The ACFs an exhibited type I isotherms on the adsorption of nitrogen or argon. Micropore analysis revealed that the ACFs have uniform micropore size distribution in which their peak diameters were in the range of $5.6{\pm}0.3{\AA}$. The BET surface area of ACFs up to $1600m^2g^{-1}$ was proportional to the adsorption capacity of iodine. The BET values of the ACFs prepared were proportional to the burn-off degree of the products.

• Journal of KIISE:Databases
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• v.28 no.4
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• pp.665-676
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• 2001

The most expensive spatial operation in patial database in a spatial join which computes a combined table of which tuple consists of two tuples of the two tables satisgying a spatial predicate. Although the execution time of sequential processing of a spatial join has been so far considerably improved the response time is not tolerable because of not meeting the requiremetns of interactive users. It is usually appropriate to use parallel processing to improve the performance of spatial join processing. in spatial database the fixed grids which consist of the regularly partitioned cells can be employed the previous works on the spatial joins have not studied the parallel processing of spatial joins using fixed grids. This paper has presented an analytical cost model that estimates the comparative performance of a parallel spatial join algorithm based on the fixed grids in terms of the number of MBR comparisons. disk accesses, and message passing, Several experiments on the synthetic and real datasets show that the proposed analytical model is very accurate. This most model is also expected to used for implementing a very important DBMS component, Called the query processing optimizer.

• Analytical Science and Technology
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• v.32 no.2
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• pp.56-64
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• 2019

Recently, a number of adulterated products, which are advertised as hair-growth enhancer have been emerged among those who suffer hair loss disease. For continuous control of illegal products, in this study, a rapid and sensitive method for simultaneous screening of 12 compounds that enhance hair-growth was established to protect public health by ultrahigh-performance liquid chromatography coupled to quadrupole-orbitrap mass spectrometry (UHPLC-Q-Orbitrap-MS). Fragmentation pathways of them were proposed based on $MS^2$ spectral data obtained using the established method. In this analysis, the LODs and LOQs ranged from 0.05 to 50 ng/mL and from 0.17 to 167 ng/mL, respectively. The square of the linear correlation coefficient ($R^2$) was determined as more than 0.995. The intra- and inter-assay accuracies were respective 88-112 % and 88-115 %. Their precision values were measured within 5 % (intra-day) and 10 % (inter-day). Mean recoveries of target compounds in adulterated products ranged from 84 to 115%. The relative standard deviation of stability was less than 12 % at $4^{\circ}C$ for 48 h. The method was employed to screen 14 dietary supplements advertised to be effective for the treatment of hair loss. Some of the products (~21 %) were proven to contain synthetic drugs that promote hair growth such as triaminodil, minoxidil, and finasteride.