• Title/Summary/Keyword: 실리케이트 수용액

Search Result 8, Processing Time 0.02 seconds

Preparation and Growth of Silica Sol from Sodium Silicate (소디움실리케이트로부터 실리카 솔 제조(製造) 및 성장(成長))

  • Yoon, Ho-Sung;Kim, Chul-Joo;Kim, Sung-Don;Jang, Hee-Dong
    • Resources Recycling
    • /
    • v.16 no.5
    • /
    • pp.31-35
    • /
    • 2007
  • The formation of silica sol from sodium silicate solution and the growth of silica sols were investigated in this study. The $SiO_2$ content of 2% in sodium silicate solution was proper to oxidize sodium silicate with sulfuric acid. After the removal of sodium ions in sodium silicate solution, the pH of silicate solution had to be controlled above 9 for a stable silicate solution. The silica sol, which size is about 10 nm, could be prepared by heating the mixed solution of sodium silicate and silicate solution removed sodium ions at pH 10 and 80. And the silica sol grew into about 50 nm as silicate solution was added to silica sol solution.

Characterization of Silica Sol Particle Prepared by Sol-Gel Reaction from Sodium Silicate Solution (소디움실리케이트 수용액(水溶液)으로부터 솔-젤 반응(反應)에 의해 제조(製造)된 실리카 솔 입자특성(粒子特性) 고찰(考察))

  • Kim, Chul-Joo;Kim, Sung-Don;Jang, Hee-Dong;Yoon, Ho-Sung
    • Resources Recycling
    • /
    • v.18 no.6
    • /
    • pp.30-37
    • /
    • 2009
  • Silica sol was prepared from the mixture of sodium silicate solution and oxidized silicate solution in which sodium had been removed by sol-gel process. The properties of sodium silicate solution and silicate solution thus prepared were characterized by yellow silicomolydate method. Moreover, the formation and growth of silica sol from sodium silicate solution was investigated. Sodium silicate solution with 2% of $SiO_2$ contains 95% of reactive silicate, and 50% of reactive silicate participates sol-gel reaction. From the results of FT-IR analysis, it was found that the intensity of silanol bond decreased and the intensity of siloxane bond increased with increasing reaction temperature. Zeta potential of silica sol prepared at each condition was -40~-60 mV and it could be known that silica sol in this study was well dispersed. The silica sol with 5~10 nm size could be prepared by heating the mixed solution of sodium silicate and silicate solution. And the silica sol grew into about 20 nm as silicate solution was added to silica sol solution.

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
    • /
    • v.31 no.2
    • /
    • pp.40-48
    • /
    • 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.

Effect of Heat Treatment and Acid Leaching of Siliceous Mudstone on the Purity of Silica Precursors (실리카 전구물질 순도에 미치는 규질이암의 열처리 및 산 침출 조건의 영향)

  • Cho, Kuk;Chang, Han-Kwon;Kil, Dae-Sup;Suh, Yong-Jae;Park, Jin-Ho;Jang, Hee-Dong
    • Journal of the Mineralogical Society of Korea
    • /
    • v.20 no.4
    • /
    • pp.247-253
    • /
    • 2007
  • The effect of heat treatment and acid leaching of siliceous mudstone on the purity of silica precursors, such as sodium silicate and silicic acid, was studied. As well as the temperatures for the heat treatment of siliceous mudstone, the concentrations of hydrochloric acid and sulfuric acid were varied to achieve the highest content of silicon in the precursors while minimizing energy and chemical consumption. It was found that the optimum conditions were achieved at the heat treatment temperature of $600^{\circ}C$ and hydrochloric acid of 1.56 M. The relative concentrations of silicon in the synthesized sodium silicate and silicic acid were as high as 99.2 and 99.5%, respectively.

Study on Performance of Lithium-Silicate Permeation and Changing Prosity Structure according to Water Content (수분의 함수율에 따른 공극구조의 변화와 리튬실리케이트의 침투성)

  • Kim, Kwang-Ki;Moon, Hyung-Jae;Kim, Jeong-Jin;Park, Soon-Jeon;Lee, Joo-Ho;Jung, Sang-Jin
    • Proceedings of the Korea Concrete Institute Conference
    • /
    • 2008.11a
    • /
    • pp.769-772
    • /
    • 2008
  • Pores can become factors of reducing the capacity of concrete by being path of degradation factors and moisture can fill up pores inside of concrete, so evaluating the effect of unidirectional permeability due to moisture on pore structure of concrete structure is very important. Therefore, the change of pore structure in cases of 0%, 40%, 60%, 80% and 90% humidity being maintained on test specimens and in case of Lithium Silicate, which is chemical compound, being coated were evaluated. As a result, the condensation due to moisture could be confirmed since unidirectional permeability was decreased and the density of Pore Structure was improved as the percentage of water content was being increased. And, solution-type Lithium Silicate fills up pores of sizes around 1$\mu$m in the condition of carrying water and improves the density but the range of capacity improvement due to osmosis will be limited according to functional conditions.

  • PDF

A Study on the Treatment of Heavy Metal in Wastewater by Redox Reaction of Cu-Zn Metal Alloy and Adsorption reaction of Al-Silicate (Cu-Zn 금속합금의 산화 환원반응과 Al-Silicate의 흡착반응을 이용한 폐수 중 중금속처리에 관한 연구)

  • Lee, Soo-Jeong;Kim, Jong Hwa;Song, Ju Yeong
    • Journal of the Korean Applied Science and Technology
    • /
    • v.33 no.3
    • /
    • pp.441-448
    • /
    • 2016
  • Heavy metal removal study is conducted from synthetic waste water by reduction and oxidation(redox) reaction of Cu-Zn metal alloy and adsorption reaction of aluminium silicate. Heavy metal whose ionization tendency is smaller than zinc are reducted in an aqueous solution, and the concentration of ionized zinc is reduced by adsorption reaction. The average diameter of metal alloy micro fiber is about $200{\mu}m$, and the surface area is wide enough to get equilibrium in a single cycle treatment. A single cycle treatment of redox reaction of Cu-Zn metal alloy, could remove 100.0 % of Cr(III), 98.0 % of Hg, 92.0 % of Sn and 91.4 % of Cu respectively. An ionization tendency of chromium is very close to zinc, but removal efficiency of chromium by redox reaction is significant. This result shows that trivalent chromium ion is expected to generate hydroxide precipitation with $OH^-$ ion generated by redox reaction. Zinc ion generated by redox reaction is readily removed by adsorption reaction of aluminium silicate in a single cycle treatment. Other heavy metal components which are not perfectly removed by redox reaction also showed very high removal efficiency of 98.0 % or more by adsorption reaction. Aluminium ion is not increased by adsorption reaction of aluminium silicate. That means heavy metal ion removal mechanism by adsorption reaction is turned out to be not an ion exchange reaction, but an adsorption reaction.

Effect of proton concentration in TEOS to improve durability of hydrophilic and high light transmittance properties of nanosilica coating (친수 및 높은 광투과 기능을 함유한 나노실리카 코팅액의 내구성 향상을 위한 수소이온 농도에 따른 TEOS의 반응 연구)

  • Lee, Soo;Chan, Sung Il;Hwang, Heon
    • Journal of the Korean Applied Science and Technology
    • /
    • v.33 no.3
    • /
    • pp.483-491
    • /
    • 2016
  • Even though the antifogging property of nanosilica coated glass surface is highly increased due to the hydrophilic hydroxyl groups on nanosilica surface, the durability of this property on outdoor glass was diminished rapidly after rain washing. In addition the topology of nanosilica coated glass surface plays very important roles to control an light transmittance or antireflection property. To improve these coating durability and characteristics a hydrophilic nanosilica coating on glass was prepared by coating with 1.5 wt% of nanosilica (Ludox) suspension in the presence of hydrolyzed tetraethylorthosilicate (TEOS). The optimum hydrolysis condition of TEOS in acidic or basic aqueous solution was also examined by contact angle measurement. The final transparent hydrophilic coating layer coated with nanosilica-TEOS in acidic condition (pH=4) showed much improved durability of hydrophilic surface as well as higher visible light transmittance than original uncoated glass by 2 % point.

Mechanical Properties of Granulated Ground Blast Furnace Slag on Blended Activator of Sulfate and Alkali (황산염 및 알칼리계의 혼합 활성화제에 대한 고로슬래그미분말의 역학적 특성)

  • Kim, Tae-Wan;Jun, Yu-Bin;Eom, Jang-Sub
    • Journal of the Korea institute for structural maintenance and inspection
    • /
    • v.19 no.5
    • /
    • pp.104-111
    • /
    • 2015
  • This study shows the mechanical properties of alkali-activated slag cement (AASC) synthesized using sulfate with NaOH solution. The used sulfates were calcium sulfate ($CaSO_4$, denoted CS) and sodium sulfate ($Na_2SO_4$, denoted SS). The replacement ratio of sulfates was 2.5, 5.0, 7.5 and 10.0% by weight of slag. NaOH solution of 2M and 4M concentration was used. A sample was activated with sulfate and activated with blended activator (blending NaOH solution with sulfate) respectively. 24 mix ratios were used and the water-binder weight ratio for the test was set 0.5. This research carried out the compressive strength, flexural strength, ultrasonic pulse velocity (UPV), absorption and X-ray diffraction (XRD). In the case of samples with CS, sample with 7.5% CS, sample with 2M NaOH+5.0% CS and sample with 4M NaOH+5.0% CS showed the good performance in the strength development. In the case of samples with SS, sample with 10.0% SS, sample with 2M NaOH+7.5% SS and sample with 4M NaOH+2.5% SS obtained good performance in strength. The results of UPV and water absorption showed a similar tendency to the strength properties. The XRD analysis of samples indicated that the hydration products formed in samples were ettringite, CSH and silicate phases. In this study, it is indicated that when compared to the use of sulfate only, the use of both sulfate and NaOH solution makes mechanical properties of AASC better.