• YAKHAK HOEJI
• /
• v.9 no.1_2
• /
• pp.14-17
• /
• 1965

It has been known that the organic base complexes formed with the anionic acid base indicators are highly soluble in non-polar solvents but relatively insoluble in water. In the work reported here the formation of the complex between chloropromazine and bromothymol blue was studied and applied it to the determination of the base. The values to determine the binding ratio of the base with the indicator at pH 3.5 obtained from the application of Job's method of continuous variation and mol ratio method were both 1:1. From the application of this reaction to the determination of the base with carbon tetrachloride as the solvent for the extraction, fairy good results have been obtained.

• Analytical Science and Technology
• /
• v.16 no.6
• /
• pp.509-512
• /
• 2003

Pretreatment method for the determination of total arsenic in seafood sample was studied. NIST SRM 1566a oyster tissue ($14.0{\pm}1.2mg\;As/kg$) as a standard arsenic compound in order to establish the decomposition method. We confirmed that the best way for pretreatment of seafoods to analyze total arsenic content precisely was $HNO_3-H_2SO_4-HCIO_4$ method by comparison of two methods which are dry ashing and wet ashing methods.

• Analytical Science and Technology
• /
• v.8 no.4
• /
• pp.535-538
• /
• 1995

This study employs the variety of mixtures of XAD resin and active carbons as concentration base for solid phase extraction (SPE) which has been widely used to preconcentrate and purify phenol and chlorophenols in determination of environmental water samples. In this study, we employed variety of mixtures of copolymer based XAD-4 resin with active carbons. This cartridges shows advantages of both materials, such as better affinity to phenol by active carbon and better mechanical stabilities from XAD resin. The better enrichment factor, pretreatment time, recoveries and limit of detection (LOD) were achieved by the attempts to pack precolumns with both meterials for preconcentration.

• Analytical Science and Technology
• /
• v.8 no.4
• /
• pp.753-758
• /
• 1995

Thermal desorption/gas chromatography/mass selective detection method using Tenax cartridges for the determination of gaseous polycyclic aromatic hydrocarbons(PAH) is described. Glass fiber filter can collect only PAH in particulate. Gaseous PAH may penetrate the filter. Glass cartridge packed Tenax-GC was uses fur adsorption of gaseous PAH. The air of inhalation zone was collected fur 2-10 hours. Cartridges were thermally desorbed in the reverse direction to sample flow. The desorption conditions were as follows; desorption temperature; $300^{\circ}C$; desorption time; 20min; column head pressure; 30psi; inlet split vent; closed during desorption.

• Analytical Science and Technology
• /
• v.8 no.3
• /
• pp.391-396
• /
• 1995

A rapid preconcentration method based on solvent extraction is described for the determination of gold by flame atomic absorption spectrophotometry. Trace amounts of gold was extracted as a new chelating agent, 3-thiophenaldehyde-4-phenyl-3-thiosemicarbazone from pH 4.0 in diisobutyl ketone. The method is simple, fast, free from the effect of many interfering ions and has a high sensitivity and a good precision. Gold is quantitatively separated and concentrated from the elements in standard sample, and the value of the recovery was 91.7 and 108.3% by the proposed method.

• Journal of Korean Society of Industrial and Systems Engineering
• /
• v.24 no.69
• /
• pp.1-12
• /
• 2001

In this paper, the consumable concurred spare parts requirement determination problem of newly procured equipment systems is considered. The problem is formulated as the operational availability maximization problem with any given fund limitation. the that the failure of a part follows a Poisson process and part failure rate is constant in spite of the decrease of number of equipments during operational period, an analytical method is developed to obtain spare part requirements using the generalized Lagrange multipliers method, The numerical examples show that analytic solution is mostly equal to the realistic solution obtained from simulation regardless of assumptions about part failure rate. It is expected that the analytical method developed in the paper can be effectively used to make a budget for provisioning the concurrent spare parts of newly procured equipment system.

• Analytical Science and Technology
• /
• v.17 no.2
• /
• pp.180-183
• /
• 2004

A simple and sensitive determination method of histidine has been investigated using the spectrofluorometry. An emission peak of $Eu^{3+}$ - TTA- histidine complex occurs at 470 nm in aquous solution with excitation at 235 nm and the fluorescence intensity increased linearly with addition of histidine in the range of $1{\times}10^{-7}-4{\times}10^{-6}M$. The detection limits was $5{\times}10^{-7}M$ with 3.5% RSD. The present method was applied to determine histidine content in the synthetic sample.

• Analytical Science and Technology
• /
• v.17 no.6
• /
• pp.532-535
• /
• 2004

A method on the determination of Co(II) after adsorbing of Co(II) on 2-mercaptobenzothiazole-loaded silica gel was studied. The conditions on the separation of Co(II) such as pH of solution, the amount of 2-mercaptobenzothiazole, the flow rate for adsorption, and the desorption solvent were optimized to 9.0, 0.05 g, $10mL\;min^{-1}$ and 1 M $HNO_3$ in ethanol, respectively. Under these optimum conditions, the calibration curve of Co(II) was obtained over concentration range of $2{\sim}120ng\;mL^{-1}$. The detection limit was $0.6ng\;mL^{-1}$. Recovery yields of Co(II) in various natural water samples were more than 90%.

• Analytical Science and Technology
• /
• v.17 no.4
• /
• pp.363-367
• /
• 2004

A simple and convenient digestion method was developed for the determination of heavy metal in polyurethane sample using only nitric acid in open system without heating. This digestion method had prevented loss of volatile elements of Hg and As and reduced the pretreatment time for the sample digestion. The detection limit is lowered over 10 times than that of microwave digestion method. Recoveries in polyurethane material were 108% for As, 96 ~ 99% for Hg, 102 ~ 103% for Cr, 98 ~ 102% for Pb, 86 ~ 90% for Cd, and 90 ~ 93% for Cu.

• Analytical Science and Technology
• /
• v.7 no.4
• /
• pp.461-469
• /
• 1994

Trace vanadium was determined by Adsorptive stripping voltammetry with HMDE in PIPES buffer solution. N-Benzoylphenylhydroxylamine was used as a ligand. The calibration curve of vanadium was linear over the range of $10{\sim}70{\mu}g/L$ on accumulation potential of +0.15V and on accumulation time of 10 sec. The various metal ions did not interfere with the determination of vanadium(V) in this case.