• Title/Summary/Keyword: Sodium Silicate

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Effect of Silicate Ions on the Hydration of 4CaO · Al2O3 · Fe2O3 with Gypsum

  • You, Kwang-Suk;Ahn, Ji-Whan;Kim, Hwan;Goto, Seishi
    • Journal of the Korean Ceramic Society
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    • v.41 no.9
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    • pp.642-646
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    • 2004
  • Na$_2$Si$_2$O$_{5}$ added to the solution affects the hydration of 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$ with calcium sulfate. The reaction between 4CaOㆍAl$_2$O$_3$ Fe$_2$O$_3$and CaSO$_4$ㆍ 2$H_2O$ decrease with increasing amount of Na$_2$Si$_2$O$_{5}$ in solution, owing to low hydraulic reactivity of 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$by the adsorption of silicate ions on the surface of 4CaOㆍAl$_2$O$_3$ㆍ Fe$_2$O$_3$ particles. The dissolution rate of 4CaOㆍAl$_2$O$_3$ㆍ Fe$_2$O$_3$ particles deceased with the increase of the concentration of silicate ion in solution. When the 4CaOㆍAl$_2$O$_3$ㆍFe$_2$O$_3$ particles was hydrated in gypsum - Na$_2$Si$_2$O$_{5}$ solution, the hydration was retarded and the rate could not discriminate between formation of ettringite and that of monosulfate, and it stopped in high concentration of silicate ions. However, silicate ion did not any effect on the dissolution rate of gypsum.ypsum.

Application of Synthetic Mineral Microparticles with Various Metal Species

  • Lee, Sa-Yong;Hubbe, Martin A.
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.40 no.5
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    • pp.1-10
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    • 2008
  • Synthetic mineral microparticles (SMM) is a patented system which has been developed to promote drainage of water and retention of fine particles during papermaking. It is shown in patents that the SMM system can have advantages in both of drainage and retention, compared with montmorillonite (bentonite), which is one of the most popular materials presently used in this kind of application. Turbidity and gravity drainage time were measured using a Britt-Jar test with representative SMM formulations, in order to confirm the efficacy of SMM covering a wide range of compositions and discover effects of some key variables that have the potential to lead to unexpected advantages in terms of the effectiveness of the microparticles, when used in combination with a cationic polyacrylamide treatment of papermaking furnish. An iron silicate showed highest retention performance, as well as suitably fast drainage time relative to other metal silicate and bentonite. Zinc silicate improved retention and drainage. SMM synthesized from aluminum sulfate ($Al_2(SO_4){_3}$) did not show a benefit in retention and drainage, relative to bentonite. SMM synthesized from aluminum chloride ($AlCl_3$) performed better in drainage and retention than bentonite when the Al/Si ratios were 0.76 and 1.00. It was found that when the Al/Si ratio and neutralization are considered, pH variation due to the change of Al/Si ratio can be a key factor to control the size of primary metal silicate particles and the degree of coagulation of the primary particles.

The Adsorption of Amines on Silicates. Distinction Protonic and Aprotonic Acids Sites (Silicate 上에서의 아민의 吸着. Protonic 酸 자리와 Aprotonic 酸 자리의 區別)

  • Kim Jong-Taik;Sohn Jong-Rack
    • Journal of the Korean Chemical Society
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    • v.20 no.6
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    • pp.441-447
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    • 1976
  • The infrared spectra obtained in the region of $4000∼1200 $cm^{-1}$ has been measured for pyridine, tertiary butylamine, and ethylenediamine adsorbed on various cation-exchanged silicates at various degassing temperature. It was possible to distinguish between protonic and aprotonic acid sites of all cation-exchanged silicates which exhibited both Bronsted and Lewis acidity. The sodium form appeared to be the least reactive towards adsorbates. The relative ratio of the band intensities of tertiary butylamine was directly related to the polarizing power of exchanged cations. Ethylenediamine was less easily desorbed from silicate surface than tertiary butylamine due to the additional amino group to react with surface active site, and probably to form ether hydrogen bond with surface oxgen by liberating migrating proton besides the coordination bond with Lewis acid site and the formation of$NH3^+$ species with Bronsted acid site.

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Evaluation of the grouting in the sandy ground using bio injection material

  • Kim, Daehyeon;Park, Kyungho
    • Geomechanics and Engineering
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    • v.12 no.5
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    • pp.739-752
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    • 2017
  • This study was intended to evaluate the improved strength of the ground by applying the bio grouting method to a loose sandy ground. The injection material was prepared in the form of cement-like powder, with the bio injection material produced by microbial reactions. The grouting test was conducted under the conditions similar to the field where the bio injection material can be applied. In addition, the injection materials (cement and sodium silicate No. 3) used for Labile Waterglass (LW) method and the conventional grouting methodwere prepared through a two-solution one-step process. The injection into the specimens was done at a pressure of 150 kPa and then, with a bender element, their moduliof elasticity were measured on the 7th, 14th, 21st and 28th curingdays to analyze their strengths according to the duration of curing. It was confirmed that in all injection materials the moduli of elasticity increased over time. In particular, when 30% of the bio injection material was added to 100% cement, the modulus of elasticity tended to increase by about 15%. This confirmed that the applicability became higher when the bio injection material was used in place of the conventional sodium silicate.

Characterization and Acid Catalytic Properties of Beryllia-Silica Catalysts (베릴리아-실리카 촉매의 특성과 산촉매성질)

  • Sohn, Jong-Rack;Park, Eun-Hee;Jang, Hyang-Ja;Kim, Hae-Won
    • Applied Chemistry for Engineering
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    • v.7 no.2
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    • pp.245-251
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    • 1996
  • A series of $BeO-SiO_2$ catalysts were prepared by coprecipitation from the mixed solution of berylium chloride and sodium silicate. The addition of BeO to $SiO_2$ caused the increased of acidity, acid strength, specific surface area, and acid catalytic activity, giving a maximum at 20 mol% of BeO. On the basis of x-ray diffraction pattern, the catalysts calcined at $400{\sim}500^{\circ}C$ were found to be amorphous, having both $Br{\ddot{o}}nsted$ and Lewis acid sites. Catalytic activities for cumene dealkylation were closely correlated with the acidity of catalysts.

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Preparation of Adsorbents Reutilizing the Leached Sludge of Red Mud (적니 침출슬러지를 재활용한 흡착제의 제조)

  • Lee, Jae-Rok;Hwang, In-Gook;Bae, Jae-Heum
    • Clean Technology
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    • v.12 no.3
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    • pp.171-174
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    • 2006
  • The adsorbent for removal of heavy metal ions is prepared reutilizing the leached sludge generated in process of making the red mud coagulant we have develope. The pellet-type adsorbent is made by heat-treating a mixture of 10g of the leached sludge, 1g of kaolin, and 2 g of sodium silicate solution at $600^{\circ}C$ for 2 hours. In experiments of batch adsorption, the adsorbent shows good performance in adsorption of $Pb^{2+}$ ion.

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Estimation of Strength and Pore Structure of Alkali-Activated Fire Protection Materials at High Temperature (고온에서의 알칼리 활성화 내화성 결합재의 강도 및 공극구조 평가)

  • Song, Hun;Kim, Young-Ho;Kim, Wan-Ki;So, Hyung-Suk
    • Journal of The Korean Digital Architecture Interior Association
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    • v.12 no.4
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    • pp.59-66
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    • 2012
  • This study is interested in identifying the effectiveness of alkali-activated fire protection material compounds including the alkali-activator such as potassium hydroxide, sodium silicate and fly ash as the fire resistant finishing materials. Also, this paper is concerned with change in compressive strength and pore structure of the alkali-activated fire protection material at high temperatures. The testing methods of fire protection materials in high temperature properties are make use of TG-DSC and mercury intrusion porosimetry measurements. This study results show that compressive strength is rapidly degraded depending on a rise of heating temperature. Porosity showed a tendency to increase irrespective of specimen types. This is due to both the outbreak of collapse of gel comprising the cement and a micro crack by heating. However, alkali-activated fire protection material composed of potassium hydroxide, sodium silicate and fly ash has the thermal stability of the slight decrease of compressive strength and porosity at high temperature. These thermal stability is caused by the ceramic binding capacity induced by alkali activation reaction by the reason of the thermal analysis result not showing the decomposition of calcium hydrate.

Multinuclear Solid-state NMR Investigation of Nanoporous Silica Prepared by Sol-gel Polymerization Using Sodium Silicate

  • Kim, Sun-Ha;Han, Oc-Hee;Kim, Jong-Kil;Lee, Kwang-Ho
    • Bulletin of the Korean Chemical Society
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    • v.32 no.10
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    • pp.3644-3649
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    • 2011
  • Multinuclear solid-state nuclear magnetic resonance (NMR) experiments were performed to investigate the local structure changes of nanoporous silica during hydrothermal treatment and surface modification with 3-aminopropyltriethoxysilane (3-APTES). The nanoporous silica was prepared by sol-gel polymerization using inexpensive sodium silicate as a silica precursor. Using $^1H$ magic angle spinning (MAS) NMR spectra, the hydroxyl groups, which play an important role in surface reactions, were probed. Various silicon sites such as $Q^2$, $Q^3$, $Q^4$, $T^2$, and $T^3$ were identified with $^{29}Si$ cross polarization (CP) MAS NMR spectra and quantified with $^{29}Si$ MAS NMR spectra. The results indicated that about 25% of the silica surface was modified. $^1H$ and $^{29}Si$ NMR data proved that the hydrothermal treatment induced dehydration and dehyroxylation. The $^{13}C$ CP MAS and $^1H$ MAS NMR spectra of 3-APTES attached on the surface of nanoporous silica revealed that the amines of the 3-aminopropyl groups were in the chemical state of ${NH_3}^+$ rather than $NH_2$.

Development of the ultra/nano filtration system for textile industry wastewater treatment

  • Rashidi, Hamidreza;Sulaiman, Nik Meriam Nik;Hashim, Nur Awanis;Bradford, Lori;Asgharnejad, Hashem;Larijani, Maryam Madani
    • Membrane and Water Treatment
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    • v.11 no.5
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    • pp.333-344
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    • 2020
  • Advances in industrial development and waste management over several decades have reduced many of the impacts that previously affected ecosystems, however, there are still processes which discharge hazardous materials into environments. Among industries that produce industrial wastewaters, textile manufacturing processes play a noticeable role. This study was conducted to test a novel continuous combined commercial membrane treatment using polyvinylidene fluoride (PVDF), ultrafiltration (UF), and polyamide (PA) nanofiltration (NF) membranes for textile wastewater treatment. The synthetic textile wastewater used in this study contained sodium silicate, wax, and five various reactive dyes. The results indicate that the removal efficiency for physical particles (wax and resin) was 95% through the UF membrane under optimum conditions. Applying UF and NF hybrid treatment resulted in total effective removal of dye from all synthetic samples. The efficiency of sodium silicate removal was measured to be between 2.5 to 4.5% and 13 to 16% for UF and NF, respectively. The chemical oxygen demand in all samples was reduced by more than 85% after treatment by NF.