• Analytical Science and Technology
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• v.11 no.2
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• pp.120-124
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• 1998

A rapid and accurate determination method of ultra-trace amounts of germanium in spring water by ICP-MS has been developed. Mass number 74 was not only the best mass but also the smallest mass interference. Only 30% of water samples contain germanium more than $0.1{\mu}g/L$, and a few of them has organogermanium species.

• Analytical Science and Technology
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• v.5 no.1
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• pp.17-24
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• 1992

Germanium(IV) was determinated in perchloric acid supporting electrolyte solution containing catechol derivates 3.4-dihydroxy benzoic acid, 3.4-dihydroxy benzaldehyde, adrenaline by hanging mercury electrode(HMDE) of anodic stripping polarography. And then to apply this experimental method for determination of germanium(IV) in natural samples. Germanium(IV) was determinated $300{\mu}g/L$ in ginseng and $210{\mu}g/L$ in mineral water.

• Journal of the Korean Chemical Society
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• v.40 no.2
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• pp.109-116
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• 1996

A matrix modification was studied for the determination of trace germanium in mineral waters by electrothermal atomic absorption spectrophotometry (ET-AAS). For this, the type and quantity of modifier as well as the use of auxiliary modifier were investigated to realize the efficient modification. Germanium suffers from low sensitivity and poor reproducibility in ET-AAS determination because of the premature loss of germanium via volatile germanium monoxide formation when heated in the presence of carbon. Therefore, the addition of a matrix modifier is necessary to stablize the germanium, thermally and chemically. By the addition of palladium (10 ${\mu}g/mL)$ as a single modifier to the sample containing 500 ng/mL germanium, the charring temperature could be raised from 800 to $1000^{\circ}C$, and its absorbance was also increased, but the atomization temperature was not raised. In this case, the absorbance of germanium was not changed in the range of 10∼70 ${\mu}g/mL$ of palladium added. On the other hand, it was considered that the use of a mixed modifier could modifiy the matrix more effectively than with a single modifier. The best results were obtained by using 1% ammonium hydroxide as an auxiliary modifier together with 10 ${\mu}g/mL$ palladium. The charring temperature could be raised from 800 to $1100^{\circ}C$, without any change of the atomization temperature. With above optimum conditions, the trace amount of germanium in several mineral waters were determined by a calibration curve method, and good recoveries of more than 95% were also obtained in the samples in which a given amount of germanium was spiked. The detection limit of this method was about 6.9 ng/mL.

• Analytical Science and Technology
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• v.10 no.3
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• pp.179-186
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• 1997

This study was carried out to improve the analytical method for determination of germanium in plants by atomic absorption spectrometry with graphite furnace. For the decomposition of plant samples, the mixed acid of $HNO_3+HClO_4+H_2SO_4$(10 : 4 : 1, v/v) was used. Under this condition, time requirement for the decomposition was 4~5 days and recovery rate was more than 98%. Solution for filling up to constant volume after decomposition was 0.1M acetic acid-sodium acetate. Detection limit for determination of germanium was 0.02 ppm by atomic absorption spectrometry with graphite furnace and argon gas. These results were corresponded with the above-mentioned research projects for improving the determination method of germanium in plants.

• Analytical Science and Technology
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• v.9 no.3
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• pp.253-261
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• 1996

Analytical method for the determination of trace germanium in inorganic matrices by differential pulse polarography(DPP) was studied. The reduction peak of germanium(IV) in perchloric acid solution containing 1, 2, 3-trihydroxy benzene appeared at -0.45V(vs. Ag/AgCl) and the peak current for germanium complex varied linearly with concentration variation. Factors affecting sensitivity and precision for germanium quantification were studied and detection limit under the investigated parameters was 1ng/ml. Inorganic samples were decomposed by fusion with potassium pyrosulfate. Serious interferences of Se(IV), Pb(II), As(III) for the determination of germanium were discussed. Interferences of these elements could be avoided by extraction of germanium from decomposed matrices by $CCl_4$ in 10M HCl solution. The germanium contents of inorganic samples(Pb bf. dust, Cu bf. dust, gneiss, Cu anode slime) were determined by the above method.

• Bulletin of the Korean Chemical Society
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• v.21 no.11
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• pp.1090-1094
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• 2000

A reaction between germanium (Ge) and the ligand, o-chlorophenylfluorone (o-CPF) has been carried out. The reaction sensitive at pH 4.5 in the presence of triton x-100 was selective in the presence of EDTA. The spectral correction technique was ap plied to the analysis of the reaction instead of single wavelength spectrophotometry because the absorption of excess of o-CPF was not negligible. An updated determination of the properties of the Ge(IV)-o-CPF complex is given, which involved the complex ratio, stepwise absorptivity and stability constant of the complex. In present work, the results show that the complex $Ge(o-CPF)_3was$ formed and its cumulative stability constant was 1.09 ${\times}$1016 . For sample analysis, the detection limit of germanium was 0.01 mg/L, and the recoveries were between 96.4% and 102%, with relative standard deviations of less than 6.5%.

• Journal of the Korean Chemical Society
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• v.37 no.11
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• pp.943-950
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• 1993

The determination of trace level germanium in 5.0 ${\times}\;10^{-2}$ M perchloric acid supporting electrolyte solution containing 8.0 ${\times}\;10^{-2}$ M catechol has been investigated by the square wave anodic stripping voltammetry. The optimum conditions in determination of germanium were as follows: deposition time; 120 sec, deposition potential; -0.9 volts vs. Ag/AgCl and frequency; 100 Hz. The determination of germanium was possible regardless of coexistent ion such as copper, lead and silicon. Calibration curve was shown a good linearlity in the range of 0.40 ppb to 2.0 ppm and the detection limit was 0.080 ppb. This method was useful for trace level germanium due to the short analysis time and higher sensitivity.

• Analytical Science and Technology
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• v.11 no.5
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• pp.400-403
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• 1998

The germanium content of the cultivated Korean medicinal herbs in several growing district was determined by adsorption stripping voltammetry. The optimum conditions in germanium determination were as following: deposition time; 120 sec, deposition potential; -0.9 volts vs. Ag/AgCl, and frequency; 100 Hz in $5.0{\times}10^{-2}M$ perchloric acid supporting electrolyte solution containing $8.0{\times}10^{-2}M$ catechol. Calibration curve was shown a good lineality in the range of 0.4 ppb to 2.0 ppm and the detection limit was 0.08 ppb. There was a large difference in content of the cultivated hermit leaf according to growing district such as 29.7~385.7 ppm and the content of nontreated hermit leaf was higher than the processed health foodstuffs. The content of the Korean ginseng (5 years) was 83 ppm while the Korean herb of life was 214 ppm.

• YAKHAK HOEJI
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• v.23 no.3_4
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• pp.141-146
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• 1979

Germanium in various botanical drugs was determined by flameless atomic absorption spectro-photometry with a graphite tube atomizer. The amounts of Ge in Zingiberis Rhizoma and Angelicae Radix were $169{\mu}g/g$ and $146{\mu}g/g$, respectively. The amounts of Ge in some other drugs ranged from $70{\mu}g/g$ to $130{\mu}g/g$. There is much more Ge in botanical drugs than in foods.

• Journal of Mushroom
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• v.2 no.3
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• pp.157-162
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• 2004

The objectives of this experiment were to study the growth and development of fruiting body of the two Ganoderma lucidum isolates on log of the soft wood Paraserianthes falcataria and the hard wood Shorea sp., and determination of organic germanium and crude ganoderic acid content of the fruiting body produced. The two Ganoderma lucidum isolates used were one Indonesian native (Indonesia isolate) and another isolate was purchased from Fungi Perfecti, USA (commercial isolate). The development and quality of the primordium and fruiting body of the mushroom, in general, were influenced by the isolates used. The types of wood, however, had no effect on the quality of the primordium and fruiting body produced. The Indonesian isolate produced better fruiting body compared to that of the commercial isolate. The development of fruiting body from primordium, however, was low for the two isolates tested. In general, only about one third of the primordium developed further into mature fruiting bodies, except for the commercial isolate grown on the soft wood medium in which more than 60% of the primordium developed into mature fruiting body. Apart from producing normal fruiting body, the commercial isolate also produced an abnormal one, which had a white mature pileus, whereas the normal one was brownish red. The organic germanium concentration of the fruiting body produced on the hard wood, in general, was higher than that of grown on the soft wood. The fruiting body from commercial isolate had higher organic germanium concentration compared to that of Indonesian isolate in both wood types. The two isolates used, however, had almost the same value of the crude ganoderic acid concentration in both types of wood tested. The Indonesian isolate had higher total yield of both organic germanium and crude ganoderic acid of the fruiting body produced compared to that of the commercial isolate.