• Title/Summary/Keyword: 염화물 수용액

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Effect of Metal Chloride Coloring Liquids on Color and Strength Changes of Tetragonal Zirconia Polycrystals (금속염화물 착색제 침투가 정방정 지르코니아 다결정체의 색조와 강도 변화에 미치는 영향)

  • Oh, Jong-Jin;Noh, Hyeong-Rok
    • Journal of dental hygiene science
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    • v.15 no.5
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    • pp.577-584
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    • 2015
  • The purpose of this study was to evaluate the effect of metal chloride infiltration treatment on color and strength changes of the yttria-stabilized tetragonal zirconia polycrystals (Y-TZP). Fifty disc specimens were prepared with a Y-TZP powder (ZPEX; Tosoh, Japan). Thirty different metal chloride solutions containing 0.03~0.08 wt% chromium and 0.03~0.07 wt% terbium ions were prepared. Presintered Y-TZP specimens were soaked in metal chloride coloring liquids for 3 minutes and sintered in air at $1,450^{\circ}C$ for 2 hours. The color of the specimens was measured with spectrophotometer and color difference (${\Delta}E^*$) was obtained based on the CIE $L^*$, $a^*$, $b^*$ color coordinate values. To evaluate the effect of metal chloride infiltration strength changes, the biaxial flexural test was performed at crosshead speed 0.5 mm/min. Colors of the sintered Y-TZP showed the colors of Vita shade guide A1, A2 and A3 with the infiltration of chromium and terbium chloride solutions. Density of the sintered Y-TZP increased by the infiltration of chromium and terbium chloride solutions. Bi-axial flexural strength of the sintered Y-TZP did not show statistically significant differences by the infiltration of chromium and terbium chloride solutions (p>0.05). Chromium and terbium chloride did not affect the crystal phase of zirconia, and all specimens showed tetragonal phase. Accordingly, this study suggests that chromium and terbium chlorides can make colored zirconia while adding in a liquid form. The color of colored zirconia differ from that of vita shade guide but it can use all ceramic restoration as substructure in dental clinic.

Relationship Analysis between Half Cell Potential and Open Circuit Potential Considering Temperature Condition (온도 영향을 고려한 RC 구조의 반 전위 및 OCP의 상관성 분석)

  • Yoon, Yong-Sik;Kwon, Seung-Jun
    • Journal of the Korean Recycled Construction Resources Institute
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    • v.10 no.1
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    • pp.124-132
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    • 2022
  • The corrosion potential in concrete varies greatly with exposure and concrete mix conditions. In this study, RC (Reinforcement Concrete) samples were prepared considering cover depth, chloride concentration, and W/C(water to cement) ratio as variables, and HCP(Half Cell Potential) was measured, which evaluated comparative potential between embedded steel and concrete surface. In addition, OCP(Open Circuit Potential) was measured using buried steel and CE(Counter Electrode). Agar and NaOH solution were used as ion exchange materials and Hg/HgO was used for RE(Reference Electrode), which was more sensitive to temperature than HCP. Among the influencing factors, the exposure period and chloride concentration had a relatively greater effect than cover depth and w/c ratio. Additionally, the entire measured HCP and OCP showed a clearly linear relationship with increasing cover depth and w/c ratio. Through multiple regression analysis, the relationship between HCP and OCP was quantified, and an improved correlation was obtained with temperature effect.

Evaluation of Chloride Extraction under Electrochemical Chloride Extraction (전기화학적 염화물 추출법에 따른 염소이온 제거 성능 평가)

  • Jiseok, Kim;Ki-Yong, Ann
    • Journal of the Korean Recycled Construction Resources Institute
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    • v.10 no.4
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    • pp.553-557
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    • 2022
  • The present study evaluate the chloride extracion under electrochemical chloride extraction method. Chloride was penetrated into the concrete from external reservoir using a 4M NaCl solution, and an electrochemical chloride extraction method was applied after the curing period of 1 year. The current density was constantly kept 1000 mA/m2 for coulostatic application with the variation in potential difference. The duration of the ECE treatment was 2, 4, 8 weeks, respectively. The residual chloride concentration at all depths decreased, and the chloride concentration decreased as the application period increased. After the application period of 8 weeks, 62.9 to 77.6 % of chloride extracted in the total chloride profile, and 77.7 to 99.5 % of chloride extracted in the free chloride profile. In particular, the concentration of free chloride at a depth of 7 mm or more from the concrete surface was 0.01 % or less by cement. In addition, it was confirmed that the bound chloride could be extracted by the electrochemical chloride extraction.

Nucleophilic Displacement at Sulfur Center (ⅩⅡ). Solvolysis of Dimethylsulfamoyl Chloride in Aqueous Binaries (황의 친핵성 치환반응 (제12보). 이성분 수용액에서의 염화디메틸술파모일의 가용매 분해반응)

  • Byong Choon Lee;Ikchoon Lee
    • Journal of the Korean Chemical Society
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    • v.24 no.5
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    • pp.342-346
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    • 1980
  • Rates and activation parameters have been determined for the solvolysis of N, N-dimethylsulfamoyl chloride in aqueous binaries of MeOH, EtOH, $(Me)_2CO$ and MeCN. Various solvent effect correlation showed that the solvolysis proceeded via the dissociative $S_n2$ mechanism.

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Effect of Concentration Polarization on The Pervaporation of Aqueous Chlorinated-Organic Solution (유기염화물 수용액의 투과증발에 미치는 농도분극의 영향)

  • Cho, Min-Suk;Kim, Seung-Jai;Kim, Jin-Hwan
    • Applied Chemistry for Engineering
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    • v.9 no.5
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    • pp.698-703
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    • 1998
  • The pervaporation experiments of aqueous solutions of trichloroethylene (TCE) and chlorobenzene (CB) through the silicone rubber (polydimethylsiloxane, PDMS) membrane were carried out and the effect of concentration polarization on the separation characteristics was investigated. The resistance-in-series model was used to explain the boundary layer resistance. It was clear that the concentration polarization phenomenon had a significant effect on the permeation behavior in the pervaporation separation of the trace organic chlorides from aqueous solutions. With the same membrane thickness, the permeation of TCE, which has a stronger affinity for the PDMS, appeared to be more influenced by the boundary layer resistance than that of CB. The effect of boundary layer resistance was reduced and the membrane resistance became dominant with increasing membrane thickness at a given hydrodynamic condition. The separation factor was increased to approach the intrinsic separation factor of the membrane with its thickness.

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Crystallization of Neodymium carbonate from Neodymium Chloride Solution (염화네오디뮴 수용액으로부터 탄산네오디뮴 결정화)

  • Kim, Chul-Joo;Yoon, Ho-Sung;Kim, Joon-Soo;Lee, Seung-Won
    • Resources Recycling
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    • v.16 no.2 s.76
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    • pp.23-31
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    • 2007
  • In this study, the crystallization of neodymium carbonate from neodymium chloride solution by addition of ammonium bicarbonate was investigated. The concentration of reactants such as neodymium chloride and ammonium bicarbonate, and reaction temperature play an important part in order to obtain the crystal of neodymium carbonate. It seemed that amorphous neodymium carbonate was prepared by aggregation of primary particles formed through nucleation. If reaction rate was increased by increasing the concentration of reactants and reaction temperature, then neodymium carbonate crystal could be obtained. Lanthanite-type neodymium carbonate[$Nd_2(CO_3)_3{\cdot}8H_2O$] and tengerite-type neodymium carbonate[$Nd_2(CO_3)_3{\cdot}2.5H_2O$] could be obtained with reaction renditions. Lanthanite-type neodymium carbonate was sensitive to temperature. The thermal decomposition of neodymium carbonate contained the processes or dehydration, decarbonation and crystalization of $Nd_2O_3$. The shape of lanthanite-type neodymium carbonate was irregular lump type, and tengerite-type neodymium carbonate had the shape of needle type. The shape of $Nd_2O_3$ was affected by the shape of neodymium carbonate.

Solvolysis of 2-Thiophenesulfonyl Chloride (2-염화티오펜술포닐의 가용매 분해반응)

  • Jin-Chel Choi;Jieun Oh;Dae Ho Kang;In Sun Koo;Ikchoon Lee
    • Journal of the Korean Chemical Society
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    • v.37 no.8
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    • pp.695-701
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    • 1993
  • Rate constants of solvolysis of 2-thiophenesulfonyl chloride were determined in aqueous binary mixtures with methanol, ethanol, acetone in water and in methanol. These data are interpreted using the equation of Grunwald-Winstein and Kivinen relationship. Also, kinetic solvent isotope effects in water and in methanol and product selectivities in alcohol-water mixtures were determined. Kinetic solvent isotope effect for hydrolysis of 2-thiopenesulfonyl chloride was 2.24 and 1.47 for methanol and water, respectively. Selectivity values for formation of ester relative to acid in ethanol-water mixtures show maximum S value. From kinetic solvent isotope effect in methanol and water, selectivity data in aqueous alcoholic solvents and solvent effects, it is proposed that the reaction channel favoured in low polarity solvents is general-base catalysis and/or is possibly addition elimination (S$_A$N) reaction pathway and in high polarity solvents iS S$_N$2 reaction mechanism.

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Linear Stability of Compositional Convection in a Mushy Layer during Solidification of Ammonium Chloride Solution (염화암모늄 수용액 응고시에 Mush 층에서 성분적 대류의 선형안정성)

  • Hwang, In Gook
    • Korean Chemical Engineering Research
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    • v.50 no.1
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    • pp.61-65
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    • 2012
  • The onset of convection in a mushy layer is analyzed by using linear stability theory in time-dependent solidification of a binary melt. A simplified model of a near-eutectic mush, in which the mush is assumed to be a porous block, is used and the propagation theory is applied to determine the critical conditions for the onset of convection. The present critical Rayleigh number is higher than the existing experimental result and also theoretical results obtained by considering the mushy layer with an overlying liquid layer. The constant pressure (permeable) condition applied on the mush-liquid interface produces a lower critical Rayleigh number, which is closer to the experimental results of aqueous ammonium chloride solution, compared with the impermeable condition.

Recovery Process of Vanadium from the Leaching Solution of Salt-Roasted Vanadate Ore (바나듐광 염배소물 수침출 용액으로부터 바나듐 회수공정 고찰)

  • Yoon, Ho-Sung;Heo, Seo-Jin;Park, Yu-Jin;Kim, Chul-Joo;Chung, Kyeong Woo;Kim, Rina;Jeon, Ho-Seok
    • Resources Recycling
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    • v.31 no.2
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    • pp.40-48
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    • 2022
  • In this study, the effects of solution components were investigated in the recovery of vanadium as ammonium metavanadate from vanadium-ore-salt roasting-water leaching solution. The vanadium-containing solution is strongly alkaline (pH 13), so the pH must be lowered to 9 or less to increase the ammonium metavanadate precipitation efficiency. However, in the process of adjusting the solution pH using sulfuric acid, aluminum ions are co-precipitated, which must be removed first. In this study, aluminum was precipitated in the form of an aluminum-silicate compound using sodium silicate, and the conditions for minimizing vanadium loss in this process were investigated. After aluminum removal, the silicate was precipitated and removed by adjusting the solution pH to 9 or less using sulfuric acid. In this process, the concentration and addition rate of sulfuric acid have a significant influence on the loss of vanadium, and vanadium loss was minimized as much as possible by slowly adding dilute sulfuric acid. Ammonium metavanadate was precipitated using three equivalents of ammonium chloride at room temperature from the aluminum-free, aqueous solution of vanadium following the pH adjustment process. The recovery yield of vanadium in the form of ammonium metavanadate exceeded 81%. After washing the product, vanadium pentoxide with 98.6% purity was obtained following heat treatment at 550 ℃ for 2 hours.

Crystallization of cerium carbonate from cerium chloride solution (염화(鹽貨)세륨 수용액(水溶液)으로부터 탄산(炭酸)세륨 결정화(結晶化) 특성(特性) 고찰(考察))

  • Kim, Sung-Don;Kim, Chul-Joo;Yoon, Ho-Sung
    • Resources Recycling
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    • v.17 no.6
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    • pp.10-16
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    • 2008
  • In this study, the crystallization of cerium carbonate from cerium chloride solution by addition of ammonium bicarbonate was investigated. The concentration of reactants such as cerium chloride(0.5-2M) and ammonium bicarbonate, and reaction temperature($20-60^{\circ}C$) have a great effect on the crystal types of cerium carbonate such as lanthanite-type cerium carbonate[$Ce_2(CO_3)_3{\cdot}8H_2O$] and tengerite-type cerium carbonate[$Ce_2(CO_3)_3{\cdot}2.5H_2O$]. The crystallinity of cerium carbonate changed from lanthanite to tengerite as the concentration of reactants and reaction temperature increased. Transformation of cerium carbonate hydrate was transformed to cerium hydroxy carbonate depended on the drying conditions. Cerium carbonate of lanthanite and tengerite has the shape of aggregates with plate type crystal, and the size of lanthanite and tengerite crystal was $3{\mu}m$ and $5{\mu}m$, respectively. Cerium hydroxy carbonate has the shape of aggregates with needle type crystal, and the crystal size was about $7{\mu}m$.