• 분석과학
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• 제20권3호
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• pp.246-250
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• 2007

The quantitative determination of chromium(VI) by separation from chromium(III) complex of 8-hydroxyquinoline using solvent extraction has been studied. The reaction conditions for chromium(III) complex of 8-hydroxyquinoline and the solvent extraction of complex were investigated in detail. The chromium(III) complex was extracted with organic solvent (n-hexane) and residual chromium(VI) was determined by ICP-AES in aqueous layer. This technique is quantitative in the pH range of 8-9 and the limitations such as interfering ions were discussed.

• 분석과학
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• 제16권1호
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• pp.25-31
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• 2003

Cr(III) picolinate는 생체이용성 물질로 동물이나 사람에게 필수 미네랄 크롬을 공급하는 물질로 알려져 있다. 본 연구에서는 두 가지 방법으로 Cr(III)- picolinate를 합성하고 원소분석, FT-IR, 고성능액체크로마토그래피 및 MALDI-MS 등으로 생성물 및 부산물의 순도와 구조를 확인하였다.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 2003년도 International Symposium on Clean Environment
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• pp.103-108
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• 2003

A method to determine chromium(III) ion in aqueous solution by chemiluminescence method using a lucigenin entrapped silica sol-gel film has been studied. An optical probe for chromium(III) ion has been prepared by entrapping lucigenin into silica sol-gel film coated on a glass support by dip coating. The chromium(III) optical sensor is based on the catalytic effect of chromium(IIII) ion on the reaction between lucigenin and hydrogen peroxide in basic solutions. The effects of Nafion, DMF and Triton X-100 were investigated to find the optimum condition to minimize cracking and leaching from the probe. The effects of pH and concentrations of lucigenin and hydrogen peroxide on the chemiluminescence intensity were investigated. The chemiluminescence intensity was increased linearly with increasing chromium(III) concentration from $2.5{\times}10^{-4}$M to $8.0{\times}10^{-7}$M and the detection limit was $4.0{\times}10^{-7}$M.

• 약학회지
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• 제13권1호
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• pp.38-42
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• 1969

Chloropentammine chromium(III) chloride를 출발물질로 하여 여러가지의 thiocyanatoammine계 착화합물을 합성하는 실험에 있어서 그 수득량이 예상보다 매우 적고 그 염의 모액이 농적자색이라는 점으로 보아 그 모액중에 어떠한 다른 착화합물이 다량 형성되어 있으리라고 추측하여 그 분리를 시도하였다든바 미려한 적자색의 결정을 얻었다. 그리고 분석에 의하여 이 물질이 potassium hexathiocyanatochromate(III) 임을 증명하였다. Cr$^{+++}$ 의 thiocyanate 착화합물형성에 관하여는 Niel Bjerrm$^{(8)}$에 의한 보고문이 있고 또 이들의 제법으로서는 Roesler$^{(9)}$들에 의하여 Potassium chromium alum에서부터 이 물질을 만드는 방법만이 보고되어 있을뿐이다. 따라서 Chloropentammine chromium(III) chloride에서 부터 이 물질을 만드는 이 새로운 방법이 이러한 화합물들의 제법으로서 앞으로 이용될 수 있는것으로 사료한다. 제조 방법: Chloropentammine chromium(III) chloride 3g을 KSCN 24g, 빙초산 24ml및 물 48ml의 혼합수용액에 현탁시킨 혼합물을 처음에는 잘 교반하면서 가온하고 다음 완전히 용해될때까지 끊인다. 냉각시킨 다음 생성된 증황색의 침반 Thiocyanatopentammine chromium(III) thiocyanate를 여과하고 여액 65ml에 KSCN 50g을 추가하여 완전용해시킨다. 이 용액을 방냉시키면 적자색의 미려한 결정이 석출되므로 이 결정을 여과하여 ethanol로 세척하고 진공 desiccator중에서 건조시켰다. 수득량 1.2~1.3g.

• 한국표면공학회지
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• 제21권4호
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• pp.160-167
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• 1988

Electrochemical behaviors od chromium electrodeposition from 0.05M chromium (III) sulface complexes in aqueous solutions using sodium formate-glycine mixtures as a complexing agent were studied. In the cathodic current-potential cures, it is found that the intial limiting current of Cr(III) is proportional to square root of scan rate and activiation energy from Arrhenius plot is s obtained 3.05Kcal/mol. From this results, the reaction is considered, Cr3++e longrightarrow Cr2+, which is controlled diffusion of Cr (III). It is also found that the chromium is deposited when the potential reaches to hydrogen evolution potential. Effects of NaSCN as a catalyser in the electrolyte were investigated NCS- anion seems to react strongly by specific absorption at the inner HelmholtZ layer, so that, it is considered to suppress the electrodeposition reaction reaction for chromjum, and also it is considered multipe-bridge such as Cr(III)-NCS---M(M;cathode).

• 한국표면공학회지
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• 제21권4호
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• pp.149-159
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• 1988

Electrodeposition of chromium from low concentration chromjum (III) sulfate complexess in aqueous using sodium formate-glycine mixtures as a complexing agent was studied. In the bath formation, it is found that the optimum again temperature and time for equilibration of the electrolytes are nrcessary for 24 hrs at 45$^{\circ}C$and the optimum elecrical charge for low current electrolysis which might be produced Cr(II) ions in the electrolytes is necessary for minum 2Ah/$\ell$. The optmun concentration off standard electrolyte for main composition is 0.05M chromium(III) sulfate, 0.2M sodium formate-0.2M glycine, and I mMNaSCN as a catalysea, respectivwly. The standard electrolyte is shows good covering, good throwing power, and 6% of current efficiency (Cr(III)basis). The oppearance of electrodeposits shows att active bright chromium. The SEM morphology of the chromjum coating is observed as smooth surfaces and dispersed micro prcro pores. X-ray diffraction analysis shows a bcc structure which the perferred orintation of the chromium electrodeposits is strongin(200)plane.

• 분석과학
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• 제13권4호
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• pp.544-547
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• 2000

By using surface modified activated alumina with AI(III) and flame atomic absorption spectrometry, a rapid and convenient method for the selective analysis of chromium (III) and chromium (VI) in water has been developed. This technique appears to work accurately under optimum pH range from 3 to 5.

• 한국암석학회:학술대회논문집
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• 한국암석학회 1999년도 춘계학술대회
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• pp.25-29
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• 1999

Manganese (Mn) oxides in soils and sediments differ in structure and composition. The influence of that diversity on the chromium (Cr) oxidation is the subject of this report. Oxidation of Cr(III) to Cr(VI) by coarse clay size Mn oxides (synthetic pyrolusite and natural lithiophorite, todorokite, and bimessite) was studied. Chromium oxidation by Mn oxides was initially fast and followed by a slow reaction. More Cr was oxidized by the Mn oxides at lower pH and higher initial Cr(III) concentration in solution. Birnessite had the highest chromium oxidation capacity per unit external surface area (COCUESA) and lithiophorite had the lowest COCUESA. The kinetics of Cr oxidation and COCUESA of Mn oixdes were apparently controlled by reactivity of surface Mn, mineralogy, and solution properties (pH and Cr(III) concentration).

• 한국결정학회지
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• 제9권2호
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• pp.143-148
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• 1998

Tris(biuret)chromium(III) Perchlorate Monohydrate (Cr(C2H5N3O2)3·(ClO4)3·H2O)의 결정 및 분자구조를 X-선 회절법으로 연구하였다. 결정의 공간군은 P, a=10.486(3) , b=11.371(5) , c=11.485(4) , α=88.70(3)o β=66.85(3)0, γ=67.11(3)o, V=1146.2(7) 3가 Z=2이다. 회절반점들의 세기는 Enraf-Noninus CAD-4 Diffractometer로 얻었으며, MoKα radiation X-선을 사용하였다. 분자구조는 직접법으로 풀었으며 최소자승법으로 정밀화하였다. 최종 신뢰도 R값은 1528개의 회절반점에 대하여 0.114이었다. Tris(biuret)chromium(III) cation은 octahedral 배열을 하고 있으며, 평균 Cr-O 결합길이는 1.94 이다. 모든 perchlorate anion은 각각 두가지 위치로 disorder되어 있다. 양이온과 음이온들은 물분자들을 포함한 수소결합들로 결합되어 결정을 이루고 있다. 양이온내의 모든 N-H가 모두 수소결합에 참여하고 있다.

• Applied Microscopy
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• 제17권1호
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• pp.29-46
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• 1987

To study hexavalent chromium effects on mitochondrial electron transport, the activities of electron transport enzymes and conformational change of mitochondria treated with $40{\mu}M$ of sodium dichromate ($Na_{2}Cr_{2}O_{7}\;2H_{2}O$) were investigated. And so were those of liver mitochondria isolated from mouse intraperitoneally injected with sodium dichromate, 40mg per kg body weight. On both treatment with chromium(VI), the activities of electron transfer enzymes (Complex I and IV) were increased to some extent and the ultrastructural transformation of mitochondria from a condensed to an orthodox conformation was inhibited under State IV respiration. These results represent' inhibitory effect of hexavalent chromium on electron transport without inhibiting electron transfer enzymes (Complex I and IV) in mitochondria. On intraperitoneal treatment with hexavalent chromium as sodium dichromate and trivalent chromium as chromic chloride, containing 37.5 mg of chromium per kg body weight, respectively, the activities of electron transfer enzymes of liver isolated from mouse with chromium(VI) was reduced, but that with chromium(III) was not affected. And with chromium(VI), all mice after 12 hours of treatment died, only after 6 hours survived. With chromium(III), however, all survived. This indicates that hexavalent chromium is more toxic than trivalent chromiumin mouse liver.