• 대한화학회지
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• 제39권2호
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• pp.87-93
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• 1995

크롬도금 용액에 공존하고 있는 Cr(III)와 Cr(VI)의 양을 자외선/가시광선 분광기에 장착한 흐름계 장치를 이용하여 시료당 5분 이내에 두 가지 물질의 양을 동시에 분석하는 방법을 개발하였다. Cr(III)와 Cr(VI)는 각각 580 nm와 440 nm에서 0.05 g/L와 0.005 g/L 이상의 범위에서 Beer-Lambert 법칙에 따르는 특성 ${\lambda}_{max}$를 나타내며, 이 파장들에서의 흡광도는 pH<4의 조건에서는 pH변화에 거의 영향을 받지 않았다. 따라서 일반적으로 크롬의 농도가 수 g/L인 후처리 크롬 도금조의 용액을 흐름계의 장치에서 pH=1의 황산 용액으로 묽힌 후, 자외선/가시광선 분광기로 측정하면 Cr(III)와 Cr(VI)의 양 및 총 크롬의 양을 기존의 산화-환원 적정 방법(최소 40분/sample)보다 간편하고 신속정확하게 동시 정량할 수 있었다. 이 장치는 설치 및 사용이 간단하고, 설치 비용이 저렴하므로 많은 도금 산업 현장에서 용이하게 응용할 수 있다.

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.634-640
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• 2005

The reaction of cis-[Cr([14]-decane)(OH$_2)_2]^+$ ([14]-decane = rac-5,5,7,12,12,14-hexamethyl-1,4,8,11-teraazacyclotetradecane) with auxiliary ligands {$L_a$ = citrate(cit)} leads to a new dimeric complex cis-[{Cr([14]-decane)($\mu$-cit)}$_2](ClO_4)_2$. This binuclear complex has been structurally characterized by a combination of elemental analysis, conductivity, IR and Vis spectroscopy, mass spectrometry, and X-ray crystallography. Analysis of the crystal structure of cis-[{Cr([14]-decane)($\mu$-cit)})($_2]^+$ reveals that each chromium has a distorted octahedral coordination environment and citrato ligands are monodentate to the two chromium atoms via the carboxyl groups. For dimeric complex the bridging geometry is as follows: Cr$\ldots$Cr = 7.361 $\AA$; Cr-O(average) = 1.958 (8) $\AA$; Cr-N range = 2.108 (9)-2.147(9) $\AA$; N(1)-Cr-N(3) (equatorial position) = 98.0(4)$^{\circ}$; N(2)-Cr-N(4) (axial position) = 166.4(4)$^{\circ}$; O(1)-Cr-N(2) = 98.1(4)$^{\circ}$; O(3)-Cr-N(4) = 96.6(3)$^{\circ}$; O(1)-Cr-O(3) = 90.4$^{\circ}$. The FAB mass spectrum of the dimeric complex displays peak due to the molecular ions cis-[{Cr([14]-decane)($\mu$-cit)})($_2]^+$ at m/z 1053.

• 한국지하수토양환경학회지:지하수토양환경
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• 제22권4호
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• pp.27-32
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• 2017

In this study, a remedial investigation using reductive stabilization was conducted to treat Cr(VI)-contaminated soil. The influences of various operational parameters, including reaction time and the mass of ferrous iron, were also evaluated. The study site was contaminated with a large amount of Cr(III) and Cr(VI), and the selected treatment method was to stabilize Cr(VI) with ferrous iron, which reduced Cr(VI) to Cr(III) and stabilized the chromium, although a greater mass of ferrous iron than the stoichiometric amount was required to stabilize the Cr(VI). However, some Cr(III) re-oxidized to Cr(VI) during the drying process, and addition of a strong reducing agent was required to maintain reducing conditions. With this reducing agent, the treated soil met the required regulatory standard, and the mass of Cr(III) re-oxidized to Cr(VI) was significantly reduced, compared to the use of only Fe(II) as a reducing agent.

• 한국토양환경학회지
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• 제4권2호
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• pp.11-31
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• 1999

회분식 및 연속류 주상 실험을 통해 인공 조제 지하수로부터 입상활성탄에 의한 6가크롬 (Cr(VI)) 제거에 대한 연구를 수행하였다. 실험에 적용된 변수로는 용액의 pH, 용존산소의 존재여부를 사용하였고 2가철(Fe(II))로 활성탄을 전처리한 것을 처리하지 않은 활성탄과 그 결과를 비교하였다. 용액의 pH를 4.0에서 7.5로 증가 시킴에 따라 무처리 및 Fe(II)로 전처리한 활성탄 모두에 흡착된 Cr(VI)의 양이 현저히 감소하였다. 용존산소가 배제 (무산소조건) 되었을 경우 Cr(VI) 제기량이 증가하였는데, 이는 Cr(VI)의 Cr(III)로의 환원 때문으로 추측된다. 그러나, Fe(II)에 의한 활성탄의 전처기는 Cr(Vl)제거에 거의 영향을 미치지 않았다 흡착된 Cr(VI)를 추출하기위해 0.01M $K_2$$HPO_4$와 침전 또는 흡착된 Cr(III)를 제거하기위해 0.02N $K_2$$HPO_4$로 세척하였는데, 이는 Cr(VI)로 흡착능이 고갈된 활성탄 재생의 한 방법으로 고려될 수 있으리라 사료된다. 재생된 활성탄은 본래의 활성탄보다 큰 흡착능을 보였는데, 그 이유는 Cr(VI)가 낮은 pH에서 흡착이 잘되며 또 Cr(III)로 환원되기 때문으로 사료된다. 산세척수중의 Cr(III)의 존재는 비교적 산성 조건하에서 Cr(VI)의 Cr(III)로의 환원을 보여주는 증거로 사료된다. 5회의 재생 및 재사용 실험에서 이 재생방법이 흡착능을 악화시키는 것 없이 지속적으로 사용될 수 있음을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제34권6호
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• pp.1625-1631
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• 2013

We report a facile synthetic approach of high-quality chromium(III) terephthalate [MIL-101(Cr)] by acetate-assisted method in the absence of toxic HF. Results indicate that the morphology and surface area of the MIL-101(Cr) can be tuned by modifying the molar ratio of acetate/$Cr(NO_3)_3$. The Brunauer-Emmett-Teller (BET) surface area of MIL-101(Cr) synthesized at the optimized condition can exceed 3300 $m^2/g$. It is confirmed that acetate could promote the dissolution of di-carboxylic linker and accelerate the nucleation ratio. So the pure and small size of MIL-101(Cr) with clean pores can be obtained. $CO_2$, $CH_4$ and $N_2$ adsorption isotherms of the samples are studied at 298 K and 313 K. Compared with the traditional method, MIL-101(Cr) synthesized by acetate-assisted method possess enhanced $CO_2$ selective adsorption capacity. At 1.0 bar 298 K, it exhibits 47% enhanced $CO_2$ adsorption capacity. This may be attributed to the high surface area together with clean pores of MIL-101(Cr).

• 대한치과보철학회지
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• 제34권1호
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• pp.125-142
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• 1996

Bond strength of four different cements to dental casting alloys which were treated with #600 emery, tin-plating, and $50{\mu}m$ sandblasting were evaluated. The alloy specimens were Type III Gold alloy(Degulor C), Palladium-Silver alloy(Pors on 4), Nickel-Chromium(Rexillium III) alloy, which were embedded in acrylic resin disc. The specimens were treated with #600 emery and tin plating, #600 emery and sandblasting, then bonded using Fuji I, Ketac Cem(Glass ionomer cements), Poly F, Livcarbo(Polycarboxylate cements). The specimens were immersed in water for 24 hours and shear bond strengths were evaluated by Instron Machine. Tin plated, sandblasted, and debonded alloy surfaces were observed using scanning electron microscope. On the basis of this study, the following conclusions could be drawn. 1. In the tin plated alloy group, increase in bond strength of glass ionomer cements was statistically insignificant. 2. In the tin plated alloy group, increase in bond strength of polycarboxylate cements was statistically significant, except nickel-chromium alloy. 3. Sandblasted alloy group showed higher bond strength than that of tin-plated alloy group.

• 마이크로전자및패키징학회지
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• 제23권4호
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• pp.79-85
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• 2016

It is imperative to find environment-friendly coatings as an alternative to the currently used hexavalent chromate conversion coatings for the purpose of improving the anti-corrosion properties of aluminum alloys. Hence, in this study, the corrosion properties of a trivalent chromate conversion coating solution are analyzed and measured. Because of the presence of multiple components in trivalent chromate conversion coating solutions, it is difficult to control plating, attributed to their mutual organic relationship. It is of significance to determine the concentrations of the components present in these coatings; hence, qualitative and quantitative analysis is required. The coating solution contained not only an environment-friendly component chromium(III), but also zirconium, fluorine, sulfur, and potassium, in the coating film. These metals are confirmed to produce a film with improved corrosion resistance to form a thin layer. The excellent corrosion resistance for the trivalent chromate solution is attributed to various inorganic and organic additives.

• Environmental Analysis Health and Toxicology
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• 제13권1_2호
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• pp.1-9
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• 1998

The ROS-producing potency of chromium compounds of several oxidation states were determined in the H4 cells. $K_2Cr_2O_7$ as Cr (VI), synthetic Cr (V) compounds and Cr (III) as TPP produced high level of ROS. However, ROS values of Cr-picolinate as Cr (III), CrCl$_2$, CrCI$_2$, were almost equal to the control. The effects of physiological antioxidants compounds which react with free radicals were examined for their effects on chromate-induced production of reactive oxygen species (ROS) in A549 cells after the addition of $K_2Cr_2O_7$. The compounds used were vitamin C (ascorbate), vitamin E ($\alpha$-tocopherol), superoxide dismutase (SOD) and catalase. The preincubation of ascorbate (200uM) with A549 cells for 20hr resulted in a significant reduction of hexavalent chromate(100uM) induced ROS. However, there is no effects of preincubation of the cells with vitamin E succinate (10 and 20uM, 20hr) on the ROS production. Also, the effects of Cr (VI) on the cell cycle of A549 cells was measured by adding the DNA intercalating agent, propidium iodide. S phase of the cell cycle was increased by the chromium (VI) compounds up to 20uM indicating toxicity or possible mitogenic action of the cell. The shoulder in Go/G1 phase at 20uM Cr (VI) with 24 hr treatment indicates apoptosis.

• 청정기술
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• 제7권1호
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• pp.75-80
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• 2001

본 연구에서는 강산성 상태에 있는 고농도의 6가 크롬 도금 폐수를 환원 및 중화의 방법으로 처리하였다. 환원제로는 강산성 상태에서 급격히 빠른 속도로 6가 크롬을 3가 크롬으로 환원시키는 황산제일철($FeSO_4$)이 사용되었고, 원수의 크롬농도에 대해 몰비로 3배의 양이 필요한 것으로 확인되었다. 환원된 3가 크롬은 석회석이 충진되어 있는 회분식 석회석탑에서 폭기에 의해 중화되었고, pH 5.0 이상으로 중화되었을 때 효과적으로 불용성의 크롬수산화물 플럭으로 형성되어 제거되는 것을 확인할 수 있었다. 이와 같은 결과들을 기초로 환원조, 석회석탑, 침전/여과조로 이루어진 6가 크롬 제거 연속공정을 개발하였고, 이 공정을 통해 6가 크롬 폐수의 연속적인 처리를 실행하였다. 석회석탑 내에서의 pH 조건이 pH 5.0 부근에서 일정하게 유지되었고, 그것으로 인해 불용성의 크롬 수산화물 플럭이 효과적으로 형성되었다. 석회석탑에서 침전조로 유도된 플럭은 침전조 내부에 부착된 1450 매쉬 크기의 기공을 지닌 금속 분리막에 의해 최종 처리수와 분리되었고, 막 여과 가동 30분 후부터 배출 허용기준을 만족시키는 크롬 농도 0.25~0.90 mg/l의 최종 처리수를 얻을 수 있었다. 막의 역세척 주기는 초기에 급격히 감소하였고, 이후에는 안정적으로 유지되었다.

• Carbon letters
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• 제9권4호
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• pp.275-282
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• 2008

Chemically activated carbons were prepared from maize cobs, using phosphoric acid of variable concentration. The textural parameters of the activated carbons were determined from the nitrogen adsorption isotherms measured at 77 K. The chemistry of the carbon surface was determined by measuring the surface pH, the pHPZC and the concentration of the carbon - oxygen groups of the acid type on the carbon surface. Kinetics of Cr(VI) sorption/reduction was investigated at 303 K. Two processes were investigated in terms of kinetics and equilibrium namely; Cr(VI) removal and chromium sorption were studied at various initial pH (1-7). Removal of Cr(VI) shows a maximum at pH 2.5. At pH<2.5, sorption decreases because of the proton competition with evolved Cr(III) for ion exchange sites. The decrease of sorption at pH>2.5 is due to proton insufficiency and to the decrease of the extent of Cr(VI) reduction. The chemistry of the surface of activated carbon is an important factor in determining its adsorption capacity from aqueous solutions particularly when the sorption process involves ion exchange.