• 제목/요약/키워드: Ion in aqueous solution

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X-Ray Diffraction Studies of Uranyl Hydrolysis Precipitates Synthesized in Neutral to Alkaline Aqueous Solutions

  • 박용준;표형렬;김원호;전관식
    • Bulletin of the Korean Chemical Society
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    • 제17권10호
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    • pp.925-929
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    • 1996
  • Uranyl hydrolysis precipitates were obtained by increasing pH value of aqueous uranyl solution in the range of neutral to alkaline pH value and their phase transformation during the solubility experiment under various conditions has been examined. The precipitates formed in the hydrolysis reaction of uranyl ion had a layered structure such as a meta-schoepite phase, a schoepite structure, or a mixed phase of meta-schoepite and schoepite. Phase transformation between them was strongly dependent on the pH value at which the precipitate was formed. The distance between the layers in meta-schoepite or schoepite phase was ∼7.35 Å, and it was increased with the pH value at which the precipitate was synthesized as well as the pH values of the aqueous solution. The phase transformation from a meta-schoepite to schoepite was fast for the precipitates formed at low pH values, however, it was not the case for the precipitates formed at high pH values. A small difference of pH value in aqueous solution gave a great change on its solubilities near pH 9.7, because a layered structure of the precipitates became amorphous above that pH value. Greater solubility for the precipitate formed at higher pH value can be explained from the fact that the precipitates formed at low pH value had a better crystallinity and also that the precipitates formed at higher pH value has a slower rate of crystallization.

강화상 나노입자의 용액 반응성이 구리 도금 박막에 미치는 영향 (Influence of Reactivity of Reinforcing Nanoparticles with Aqueous Solution on Electroplating Copper Films)

  • 박지은;오민주;김이슬;이동윤
    • 한국재료학회지
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    • 제23권12호
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    • pp.695-701
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    • 2013
  • To understand how reactivity between reinforcing nanoparticles and aqueous solution affects electrodeposited Cu thin films, two types of commercialized cerium oxide (ceria, $CeO_2$) nanoparticles were used with copper sulfate electrolyte to form in-situ nanocomposite films. During this process, we observed variation in colors and pH of the electrolyte depending on the manufacturer. Ceria aqueous solution and nickel sulfate ($NiSO_4$) aqueous solutions were also used for comparison. We checked several parameters which could be key factors contributing to the changes, such as the oxidation number of Cu, chemical impurities of ceria nanoparticles, and so on. Oxidation number was checked by salt formation by chemical reaction between $CuSO_4$ solution and sodium hydroxide (NaOH) solution. We observed that the color changed when $H_2SO_4$ was added to the $CuSO_4$ solution. The same effect was obtained when $H_2SO_4$ was mixed with ceria solution; the color of ceria solution changed from white to yellow. However, the color of $NiSO_4$ solution did not show any significant changes. We did observe slight changes in the pH of the solutions in this study. We did not obtain firm evidence to explain the changes observed in this study, but changes in the color of the electrolyte might be caused by interaction of Cu ion and the by-product of ceria. The mechanical properties of the films were examined by nanoindentation, and reaction between ceria and electrolyte presumably affect the mechanical properties of electrodeposited copper films. We also examined their crystal structures and optical properties by X-ray diffraction (XRD) and UV-Vis spectroscopy.

$MgCl_2$ 수용액 중에서 SUS 304강의 SCC 특성에 관한 연구 (An Investigation of Stress Corrosion Cracking Charactistics of SUS 304 Stainless Steel in $MgCl_2$ Aqueous Solution)

  • 임우조
    • 수산해양기술연구
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    • 제20권2호
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    • pp.133-136
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    • 1984
  • 정변위 인장시험기를 사용하여 SUS 304강 용접열 영향부의 여러 가지 염화 마그네슘용액 중에서의 SCC 발생 특성을 연구한 결과 다음과 같은 결론을 얻었다. 1) SCC 발생 잠복기간은 초기 응력강도계수 K 하(Ii) 값은 낮게 함으로써 크게 지연된다. 2) 비등 염화 마그네슘 용액 중에서의 SCC 발생은 부하와 Cl 이온의 농도에 의한 부동태 피막의 파손에 기인된다. 3) SUS 304 강 용접열 영향부의 SCC 발생 감수성은 높은 농도의 염화 마그네슘 용액일수록 온도를 낮게 함으로써 둔화된다.

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전해질 수용액의 고온 열역학 (High Temperature Thermodynamics of Aqueous electrolyte Solutions)

  • 이만승
    • 자원리싸이클링
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    • 제27권2호
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    • pp.63-67
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    • 2018
  • 자유에너지는 물질의 상대적인 안정도를 나타낸다. 수용액에 존재하는 이온의 종류는 다양하고 실험조건이 광범위하므로 열역학 자료가 부족하다. 이온의 표준생성엔탈피와 엔트로피로부터 표준수화엔탈피와 표준수화엔트로피의 절대값과 상대값을 구하는 방법을 설명하였다. 또한 대응원리를 이용하여 고온에서 열역학 자료를 추산하는 방법을 설명하였다.

Effect of Residual Lithium Ions on the Structure and Cytotoxicity of Silk Fibroin Film

  • Yang, Yesol;Kwak, Hyo Won;Lee, Ki Hoon
    • International Journal of Industrial Entomology and Biomaterials
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    • 제27권2호
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    • pp.265-270
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    • 2013
  • Dialysis is the rate-limiting step in the preparation of aqueous silk fibroin (SF) solution. However, the traditional practice of dialyzing SF solution for at least 48 h to remove LiBr is not based on empirical evidence. The aim of the present study was to systematically measure LiBr content in SF solutions dialyzed for varying lengths of time and assess the potential toxicity of residual lithium ions in cells. Complete removal of lithium ions was not achieved even after 72 h of dialysis, with a residual lithium ion content in the solution of 22.85 mg/l. SF films prepared from solutions dialyzed for 8 and 24 h had predominantly random coil or b-sheet structures, respectively. The residual lithium had little cytotoxicity in NIH3T3 fibroblast cells, but viability was compromised in cells grown on SF film prepared from solution dialyzed for 24 h.

수용액 중에서 Polyamine계 유기응집제를 이용한 중금속 이온의 흡착 - 키토산의 분자량과 탈아세틸화도 - (An Investigation for the Adsorption of Heavy Metal Ions by Polyamine Organic Adsorbent from the Aqueous Solution - The Influence of Molecular Weight and Degree of Deacetylation of Chitosan -)

  • 박영미;전동원
    • 한국의류산업학회지
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    • 제8권4호
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    • pp.458-464
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    • 2006
  • The adsorption ability of heavy metal ions from the aqueous solution by chitosan, which it is well known natural biopolymer, has been investigated. The fundamental study in this research is focusing on the physicochemical adsorption utilizing the chitosan as a organic chelating adsorbent, adsorb especially heavy metal ions from the waste liquid solution. The adsorption ability of the chitosan between metal ions, having different characteristics with Mw of 188,600, 297,200, and 504,200 g/mol and degree of deacetylation (DD) of 86.92% and 100% were investigated targeting on the $Ni^{2+}$, $Co^{2+}$, $Zn^{2+}$, and $Pb^{2+}$ ions, respectively. The uptake of heavy metal ions with chitosan was performed by atomic absorption flame emission spectrophotometer (AAS) as conducted residual metal ions. It was found that chitosan has an strong adsorption capacity for some metals under certain conditions. Chitosan, which have 100% degree of deacetylation showed high adsorption recovery ratio and have an affinity for all kinds of heavy metals. In contrast, the molecular weight of chitosan was not completely affected on metal ion adsorption.

식물 잎을 이용한 중금속 이온의 제거에 관한 연구 (Removal of Heavy Metal Ions from Aqueous Solution by Leaves)

  • 김종규;이장훈;이수영;나경원;나규환;최한영
    • 환경위생공학
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    • 제24권2호
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    • pp.31-39
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    • 2009
  • In this research, I carried out the adsorption and removal test of Pb, Ni, Co and Cu ions using organic substances spread out any where in the nature which can be obtained easily from our neighbor-such as Paulownia coreana, Pinus densiflora, Juniperus chinesis, Quercus dentata, Magnolia kobus, Platanus occidentalis, Gingko biloba, Diospyros kaki leaves. As the result of the research to find the best optional condition for the adsorption and removal, shows that the adsorption and removal ratio of Pb ion by a Paulownia coreana raw leaves is 99% at $70^{\circ}C$, those of Ni ion and Co ion by Magnolia kobus formalin treatment leaves are 79% at $70^{\circ}C$, 97% at $40^{\circ}C$ respectively. And that of Cu ion by Platanus occidentalis treatment leaves is 97% at $50^{\circ}C$ in mixed solution. As the result of comparing the removal ratio by raw leaves and formalin treatment leaves, the removal ratio of treatment is 30~90% more effective than raw leaves in most cases. And I concluded Pb > Cu > Co > Ni ion in multiple solution and Co > Ni > Cu >Pb ion in single solution after testing adsorption and removal ratio of mixed solution separately as time goes by. In general, the reactions were completed within first 5 minutes. The test result of measuring the hydrolysable tannin content of each leaf shows that an overcup Quercus dentata is 11.36%, a Diospyros kaki is 10.81% and the rest of them are 2.49~4.12% in raw leaves cases. In treatment leaves cases, an overcup Quercus dentata is 3.23% and the others are less than 1%.

Quercetin의 카드뮴 착물반응에 대한 최적농도 (Optimum Concentration of the Cd(II)-Quercetin Complexation Reaction)

  • 이정호;신선우;백승화
    • 약학회지
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    • 제53권5호
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    • pp.235-240
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    • 2009
  • The interaction of cadmium (II) ion with quercetin was investigated in aqueous solution at different pH. The quercetin/cadmium stochiometries for cadmium (II) binding have been determined by UV-vis spectrophotometric method. The complexation of Cd(II) ion with 54.72 ${\mu}M$ quercetin (A=1.00793) was formed in 0.2 M $NH_3-0.2$ M $NH_4Cl$ (pH 8.0) buffer solution. 1:1 Cd(II)-complex had a maximum absorbance and showed the bathochromic shift of the long-wavelength band of the UV-vis spectra in the alkaline pH when interacted with quercetin in buffer solution. These results suggest that Cd(II)-quercetin complex has the optimal condition of chelation in basic buffer solution.

액체막형 구리이온 선택성 전극의 제작과 전위차적정에의 응용 (Preparation of a Liquid Membrance Type Ion-Selective Electrode and Its Application to the Potentiometric Titration)

  • 이흥낙;양승태
    • 대한화학회지
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    • 제29권2호
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    • pp.137-143
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    • 1985
  • 액체막형 구리이온 선택성 전극의 제작과 전위차적정에의 응용을 연구하였다. 액체 이온교환막은 수용액속의 Cu(II)을 1-(2-pyridylazo)-2-naphthol/nitrobenzene 용액 속으로 추출하여 만들었다. 액체 이온교환막 위에 HAc-NaAc 용액으로 완충된 $1.00 {\times} 10^{-3}M\;Cu(NO_3)_2$ 용액을 채우고 Ag/AgCl 내부 기준전극을 담그었다. 이 이온선택성 전극은 $1.00 {\times} 10^{-6}$ ~ $1.00 {\times} 10^{-3}$M Cu(II) 농도 범위에서 nerstian response를 보여주었다. 가장 적절한 이온교환체의 농도는 $1.00 {\times} 10^{-4}$M이었다. 여러가지 금속이온에 대한 이온선택성 전극의 선택계수를 측정하였다. EDTA를 적정제로 하여 Cu(II)에 대한 전위차적정에 응용하였다.

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태양전지용 CdSe 나노입자의 합성 (Preparation and Characterization of CdSe nanoparticle for Solar Cell application)

  • 김신호;박명국;이보람;이현주;김양도
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 추계학술대회 논문집
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    • pp.318-321
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    • 2007
  • CdSe nanoparticles were prepared by chemical solution methods using $CdCl_2{\cdot}4H_2O$ (or $Cd(NO_3)_ 2{\cdot}4H_2O$) and $Na_2SeSO_3$. The characteristics of CdSe nanoparticles were controlled by the react ion time, reaction temperature and reaction method as well as the surfactants. Cetyltrimethyl ammonium bromide(CTAB) was used as a capping agent to control the chemical reactions in aqueous solution. Polyvinylalcohol(PVA) was used as a templet in sono-chemical method. CdSe nanoparticles synthesized in aqueous solution showed homogeneous size distribution with relatively stable surface. CdSe nanoparticles synthesized in non-aqueous solution containing diethanolamine(DEA) showed the structure transformation from cubic to hexagonal as the reduction temperature increased from 80 to $160^{\circ}C$. Core shell CdSe was synthesized by sono-chemical method. Characteristics of CdSe nanoparticles were analyzed using transmission electron microscopy(TEM), x-ray photoelectron spectroscopy(XPS), x-ray diffraction(XRD), UV-Vis absorption spectra, fourier transform infrared spectroscopy(FT-IR) and photoluminescence spectra spectroscopy(PL). This paper presents simple routes to prepare CdSe nanoparticles for solar cell applications.

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