• 한국결정성장학회지
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• 제27권5호
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• pp.243-248
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• 2017

본 연구에서는 산화주석(IV) 첨가량을 달리하여 동화유약 시편을 제조하고 발색기구를 분석하기 위하여 분광 분석, 결정상 분석, 미세구조 분석을 실시하여 색상과의 상관성을 분석하였다. 산화주석(VI) 첨가량이 증가함에 따라 동화유약의 붉은색은 사라지고 CIEab 값이 감소하여 무채색으로 발색하였다. 산화주석은 유약층에 고르게 분포하여 Cu nuclei가 성장하여 붉은색으로 발색하는 것을 방해하고 기포 주변의 metal Cu와 반응하여 합금을 형성하였다. 이로 인해 산화주석 첨가량이 증가함에 따라 금속 Cu 피크는 사라지고 미세한 $Cu_2O$ 피크만 남게 된다. 산화주석을 3.79 % 첨가하였을 때는 유약에 붉은색을 내는 $Cu_2O$보다 검정색을 나타내는 CuO와 Cassiterite $SnO_2$가 색상에 더 영향을 미치는 것으로 보여진다.

• 대한화학회지
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• 제56권1호
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• pp.54-57
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• 2012

New Schiff base derivatives of organoheterobimetallic-${\mu}$-oxoisopropoxide $[Bu_2SnO_2Ti_2(OPr^i)_6]$ have been synthesized by the thermal condensation ${\mu}$-oxoisopropoxide compound with Schiff bases in different molar ratios (1:1-1:4) yielded the compounds of the type $[Bu_2SnO_2Ti_2(OPr^i)_{6-n}(SB)_n]$ (where n is 1-4 and SB=Schiff base anion) respectively. The ${\mu}$-oxoisopropoxide derivatives have been characterized by elemental, spectral analysis (IR, $^1H$, $^{13}C$, $^{119}Sn$ NMR) and molecular weight measurement The studies reveal that the derivative compounds show monomeric nature. Further these are found less susceptible to hydrolysis as compared to parent compound and may prove excellent precursors for the mixed metal oxides.

• 대한금속재료학회지
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• 제48권5호
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• pp.430-435
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• 2010

Solvent extraction experiments of Rh(III) and Ir(IV) were performed on the HCl solution by using Alamine336 and TBP. The extraction percentage of Rh and Ir by Alamine336 was much higher than that by TBP. For the solvent extraction with Alamine336, the extraction percentage of Rh and Ir decreased with a HCl concentration. However, the extraction percentage of both metals by TBP was below 12% in our experimental range and increased with an increasing HCl concentration of up to 8 M. From the mixed solution of Ir with an excess SnCl$_{2}$, most of the tin was extracted by Alamine336 and TBP. However, the extraction percentage of Ir by Alamine336 was reduced and no iridium was extracted by TBP. The extraction behavior of Ir and Sn was investigated by scrubbing experiments on the loaded Ir with a SnCl$_{2}$ solution.

• 대한치과보철학회지
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• 제33권4호
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• pp.685-692
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• 1995

The effect of five different surface treatments on the shear bond strength of the resin bond to Type IV Gold alloy was studied by bonding resin to metal. The metal surface was subjected to one of the following treatments and bonded ;(1) air abraded with $50{\mu}m$ alumina particles,(2) beads(3) beads and tin-plated at curreant density of 300mA/$cm^2$,(4) tin-plated at current density of 300mA/$cm^2$,(5) silicacoating with sililink, and bonded with an MDP Opaque primer, CESEAD resin system. The bonded specimens were immersed in water for 23 hours after 1 hour resin curing and shear bond strength were recorded. On the basis of this study, the following conclusions can be drawn; 1. Difference were found in the shear bond strength among all experimental groups. And bead glroup exihibited the highest shear bond strength and sand blasting group exhibited the lowest shear bond strength on five groups. 2. Bead group, mechanical bonding was significantly higher than that obtained with the samples, tinplating, silicacoating, and chemical bonding. 3. No statistically signiflcant difference was found between the shear bond strengths obtained with bead and bead-tinplating, and between tinplating and sili cacoating.

• 한국세라믹학회지
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• 제46권6호
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• pp.708-712
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• 2009

ITO films were achieved by sintering at $500{\sim}550{^{\circ}C}$. This was possible by inducing a seeding effect on an ITO sol by producing crystalline ITO nanoparticles in situ during heat treatment. Two kinds of ITO sols (named ITO-A and ITO-B) were prepared at 2.0 wt% from indium acetate and tin(IV) chloride in different mixed solvents. The ITO-A sol showed a high degree of crystallinity of ITO without any detectable Sn$O_2$ on XRD at $350{^{\circ}C}$/1 h, but the ITO-B sol showed a small amount of Sn$O_2$ even after annealing at $600{^{\circ}C}$/1 h. The 10 wt% ITO-A//ITO-B showed the sheet resistance of 3600$\Omega$/□, while the ITO-B sol alone showed 5200 $\Omega$/□ by sintering at $550{^{\circ}C}$ for 30 min. Processing parameters were studied by TG/DSC, XRD, SEM, sheet resistance, and visible transmittance.

• 자원리싸이클링
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• 제19권3호
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• pp.45-51
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• 2010

염산용액으로부터 TBP(Tri-butyl Phosphate)를 사용하여 주석(IV)의 추출에 대한 기초연구를 실시하였다. 수용액상에서 염산과 염소이온($Cl^-$) 농도, 주석 농도 및 추출제 농도 등과 같은 실험인자들이 주석의 추출에 미치는 영향을 조사하였다. 염산과 염소이온 농도가 증가할수록 주석의 추출율이 증가하였고, 7.0M의 염산농도에서 10% TBP에 의해 주석이 98%이상 추출되었다. McCabe-thiele 도표 분석을 통해 주석의 연속 추출에 필요한 이론적인 최적 추출단수를 구하였다. 한편 탈거액으로 NaOH 용액이 효과적이었고, 2.0M NaOH 에서 99.3%이상의 높은 탈거율을 나타냈다.

• 한국의학물리학회지:의학물리
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• 제6권2호
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• pp.35-40
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• 1995

목적 : 필름배지를 이용하여 개인 피폭 선량을 측정하는 방법을 개발하고 그 특성을 알아보고자 한다. 재료 및 방법 : 필름으로는 Agfagaevart Personal monitoring 2/10 을 사용하였고, 필터로는 구리 0.3mm, 플라스틱 1.5mm, 알루미늄 0.6mm, 주석 0.8mm를 사용하였으며, 필름은 표준기관에서 교정하였다. 사용에너지는 ANSI N13.11 Category III, IV였고, 현상기는 수동현상기를, 농도계는 Xrite 농도계를 사용하였다. H＆D 곡선을 선량에 따라 구한 뒤 다항식 전개를 이용하여 선량에 대해 직선성을 갖도록 변환하였다. 이후 필터와 방사선 에너지 관계를 구하여 선량 및 에너지를 추정할 수 있는 알고리즘을 개발하였다. 결과 : 본 연구에서 개발된 선량 평가 알고리즘은 해당 Category 의 전에너지에 대해 30% 이내의 정확도를 만족시켜 이 알고리즘이 개인 피폭 선량 측정에 이용될 수 있음을 알았다. Category I, II , V에 대하여 보완한다면 완벽한 선량 평가 알고리즘이 될 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제32권9호
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• pp.3295-3305
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• 2011

Thermal behavior of poly (methyl methacrylate) was analyzed in the presence of tin (IV) chloride. Five different proportions - polymer to additive - were selected for casting films from common solvent. TG, DTG and DTA were employed to monitor thermal degradation of the systems. IR and py-GC-MS helped identify the decomposition products. The blends start degrading at a temperature lower than that of the neat polymer and higher than that of the pure additive. Complex formation between tin of additive and carbonyl oxygen (pendent groups of MMA units) was noticed in the films soon after the mixing of the components in the blends. The samples were also heated at three different temperatures to determine the composition of residues left after the expulsion of volatiles. The polymer, blends and additive exhibited a one step, two-step and three-step degradation, respectively. $T_0$ is highest for the polymer, lowest for the additive and is either $60^{\circ}C$ or $70^{\circ}C$ for the blends. The amount of residue increases down the series [moving from blend-1 (minimum additive concentration) to blend-5 (maximum additive concentration)]. For blend-1, it is 7% of the original mass whereas it is 16% for blend-5. $T_{max}$ also goes up as the concentration of additive in the blends is elevated. The complexation appears to be the cause of observed stabilization. Some new products of degradation were noted apart from those reported earlier. These included methanol, isobutyric acid, acid chloride, etc. Molecular-level mixing of the constituents and "positioning effect" of the additive may have brought about the formation of new compounds. Routes are proposed for the appearance of these substances. Horizontal burning tests were also conducted on polymer and blends and the results are discussed. Activation energies and reaction orders were calculated. Activation energy is highest for the polymer, i.e., 138.9 Kcal/mol while the range for blends is from 51 to 39 Kcal/mol. Stability zones are highlighted for the blends. The interaction between the blended parts seems to be chemical in nature.

• 한국재료학회지
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• 제21권8호
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• pp.415-418
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• 2011

Tin (IV) dioxide ($SnO_2$) has attracted much attention due to its potential scientific significance and technological applications. $SnO_2$ nanoparticles were prepared under low temperature and pressure conditions via precipitation from a 0.1 M $SnCl_4{\cdot}5H_2O$ solution by slowly adding $NH_4OH$ while rapidly stirring the solution. $SnO_2$ nanoparticles were obtained from the reaction in the temperature range from 130 to $250^{\circ}C$ during 6 h. The microstructure and phase of the synthesized tin oxide particles were studied using XRD and TEM analyses. The average crystalline sizes of the synthesized $SnO_2$ particles were from 5 to 20 nm and they had a narrow distribution. The average crystalline size of the synthesized particles increased as the reaction temperature increased. The crystalline size of the synthesized tin oxide particles decreased with increases in the pH value. The X-ray analysis showed that the synthesized particles were crystalline, and the SAED patterns also indicate that the synthesized $SnO_2$ nanoparticles were crystalline. Furthermore, the morphology of the synthesized $SnO_2$ nanoparticles was as a function of the reaction temperature. The effects of the synthesis parameters, such as the pH condition and reaction temperature, are also discussed.

• 한국세라믹학회지
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• 제44권11호
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• pp.650-654
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• 2007

[ $SnO_2$ ]-doped $TiO_2$ thin films were prepared from tin (IV) bis (acetylacetonate) dichloride and titanium diisopropoxide bis (acetylacetonate) with pluronic P123 or degussa P25 as a structural-directing agent. These hydrolyzed sol were spin coated onto Si(100) wafer substrate. The microstructure, morphology and bonding states of thin films were studied by field-emission scanning electron microscopy (FE-SEM), X-ray diffractometry (XRD), and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of these films was investigated by using indigo carmine solution.