• Title/Summary/Keyword: Calcium carbonate($CaCO_3$)

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A Novel Method for Calcium Hardness Control of Closed OCC Recycling System

  • Ow, Say-Kyoun;Shin, Jong-Ho;Song, Bong-Keun;Ryu, Jeong-Yong
    • Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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    • 1999.11b
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    • pp.164-171
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    • 1999
  • A new technique for recycling process water was developed in order to reduce the calcium hardness of the closed OCC recycling system. Calcium ions present in the white water were precipitated as calcium carbonate by a reaction with sodium carbonate and the CaCO$_3$precipitates were easily removed from the system by a dissolved air flotation(DAF) method. After the DAF stage, CO$_2$-gas was purged into the water because the pH of Na$_2$CO$_3$-treated white water was reduced to neutral by CO$_2$gas. Since CaCO$_3$precipitate tends to stick onto the fine fiber surface and then is selectively removed from the water, a proper amount of suspended solid in the process water acts as an important factor in deciding the removal efficiency. By the application of Na$_2$CO$_3$addition - DAF - CO$_2$purging to the short circulated white water the calcium hardness was significantly reduced by 92% and more. The removal of calcium ions with fine fibers led to drainage improvement, reduction of fresh water consumption, and enhanced efficiency of wet-end chemicals.

Synthesis of aragonite precipitated calcium carbonate by homogeneous precipitate reaction of $Ca(OH)_2\;and Na_2CO_3$ ($Ca(OH)_2\;및 \;Na_2CO_3$수용액의 균일침전 반응에 의한 아라고나이트 침강성 탄산 칼슘의 합성)

  • Park, Jin-Koo;Park, Hyun-Seo;Ahn, Ji-Whan;Kim, Hwan;Park, Charn-Hoon
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.14 no.3
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    • pp.110-114
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    • 2004
  • Formation behavior of aragonite precipitated calcium carbonate was investigated with changed the concentration of $Na_2CO_3$ solution and addition method which added in the $Ca(OH)_2$ slurry at $75^{\circ}C$. In this reaction, we found that $Na^+$ ions were substituted into $Ca^{2+}$ion site then disturb the growth of calcite, and while proceed the crystal growth in a certain direction and promote the formation of aragonite. Also, a decrease of reaction rate by control the concentration of $CO_3^{2-}$ ion, induce the homogeneous precipitate reaction and increase substitution ability of $Na^+$ ions, consequently it was promote the formation and growth of aragonite.

Influence of Thallium Carbonate on the Hydration of Tricalcium Silicate (Tricalcium silicate의 수화반응에 따른 $T1_2CO_3$의 영향)

  • Yim, Going
    • The Journal of Natural Sciences
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    • v.4
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    • pp.95-102
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    • 1991
  • The influences of various concentrations of thallium carbonate on the hydration of tricalcium silicate which is widely used to the inorganic materials have been studied using an isothermal microcalorime-ter. The experimental results indicate that the hydration of tricalcium silicate is accelerated in the presence of thallium carbonate, namely the concentration of thallium carbonate is increased, the rate of hydration is also increased. The x-ray diffraction analysis shows that the concentration of tricalcium silicate decreases rapidly in the presence of thallium carbonate. Differential thermal analysis of tricalcium silicate hydrated in the persence of thallium carbonate indicates the presence of calcium carbonate. The nonevaporable water content and the degree of hydration of tricalcium silicate show that the accelerating action of thallium carbonate is more pronounced only during the early period of hydration. Analytical results of the liquid phase in contact with the tricalcium silicate paste indicate that the concentrations of calcium and hydroxyl ions are changed considerably in the presence of thallium carbonate.

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Morphological Analysis of Engineered PCC by Gas-Liquid Mixing Conditions (기체-액체 혼합조건에 따른 Engineered PCC의 형태학적 분석)

  • Lee, Tai-Ju;Seo, Jin-Ho;Kim, Hyoung-Jin
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.43 no.3
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    • pp.113-120
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    • 2011
  • Precipitated calcium carbonate(PCC), particularly calcite crystal, is extensively used as a pigment, filler or extender in various industries such as paper, paint, textile, detergents, adhesives, rubber and plastics, food, cosmetics, and biomaterials. PCC is conventionally produced through the gas-liquid carbonation process, which consists on bubbling gaseous $CO_2$ through a concentrated calcium hydroxide slurry. This study is aimed to find some factors for controlling the morphology of engineered PCC in lab-scaled mixing batch. The experimental designs were based on temperature variables, $Ca(OH)_2$ concentration, $CO_2$ flow rate, and electrical conductivity. The model of engineered PCC morphology was finally controlled by adjustment of electrical conductivity(6.0~7.0 mS/cm) and $Ca(OH)_2$ concentration(10 g/L). Orthorhombic calcite crystals were mostly created at high concentration and electrical conductivity conditions because the increased ratio of $Ca^{2+}$ and $CO{_3}^{2-}$ ions affects the growth rate of orthorhombic faces. Excess calcium spices were contributed to the growth of faces in calcium carbonate crystal, and the non-stoichiometric reaction was occurred between $Ca^{2+}$ and $CO{_3}^{2-}$ ions during carbonation process.

The effect of mixing of calcium superphosphate, urea and lime on the change of the available phosphate and urea-nitrogen (과인산석회(過燐酸石灰)와 요소(尿素) 및 농용(農用) 석회(石灰)의 배합(配合)에 의한 유효성인산(有效性燐酸) 및 요소태(尿素態) 질소(窒素)의 변화(變化)에 관(關)한 연구(硏究))

  • Maeng, Do-Won
    • Applied Biological Chemistry
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    • v.7
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    • pp.45-52
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    • 1966
  • This study was carried out to determine how the water soluble, the available $P_2O_5$ and urea-N would change in the course of time, when the mixtures of calcium superphosphate and urea with lime for fertilizer which occurred in Korea and largely contained calcium carbonate were made. Three kinds of materials, i. e., calcium superphosphate, urea and lime for fertilizer were used in this study. Three kinds of mixed fertilizer, i. e., A, B and C were made up by mixing these materials to satisfy the following formula. $$1)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_2H_2(PO_4)+H_2CO_3+NH_3$$ $$2)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_3(PO_4)_2+H_2CO_3+NH_3$$ $$3)\;Ca(H_2PO_4)_2+CaCO_3+CO(NH_2)_2{\rightarrow}$$$$Ca_3(PO_4)_2+H_2CO_3+CaCO_3+NH_3$$ A,B and C were placed in desiccators respectively a six month period. During the time of storage, the water soluble, the available phosphoric acid and urea-N were measured once a month, seven times with the control measurement. The results may be summarized as follows. 1. None of A, B and C showed any change in the urea-N with the lapse of time. This fact indicated that the combination of calcium superphosphate and urea with lime for fertilizer was not unfavourable. 2. A, B and C decreased in the amount of water soluble $P_2O_5$ with the passage of time. This fact indicated that the mixing of calcium superphosphate and urea with lime for fertilizer was unfeasible. 3. The available $P_2O_5$ in any of A,B and C did not undergo a change as time went by. This fact suggested that the combination of calcium superphate and urea with lime for fertilizer was favourable.

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Cell Wall Micropore Loading of Pulp Fibers (펄프 섬유의 세포벽 미세공극 충전)

  • Lee, Jong-Man;Jo, Byoung-Muk
    • Journal of the Korean Wood Science and Technology
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    • v.20 no.4
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    • pp.57-64
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    • 1992
  • The unique cell wall micropores of pulp fiber can be utilized as loading site in variety of important practical application which could be the basis of new papermaking technologies. One of these includes the manufature of paper containing higher levels of in situ filler precipitated. Hardwood pulp fiber were first impregnated with the solution of sodium carbonate($Na_2CO_3$). The micropores in cell wall of pulp fibers were filled with the liquid salt solution. The second calcium nitrate($Ca(NO_3)_2$) solution formed an insoluble calcium carbonate($CaCO_3$) precipitate within the cell wall micropores by interacting with the first sodium carbonate solution. The effects of chemical concentration and dryness of pulp fibers on the retention of cell wall micropore loaded filler were investigated. The paper properties of cell wall micropore loaded pulp fibers were compared with those of conventionally loaded and lumen loaded pulp fibers. Also the presense of the fillers within the cell wall micropore was observed by SEM. Increasing the chemical concentration to generate the calcium carbonate increased the retention of filler in cell wall micropore loaded pulp fibers. The particle size distribution of precipitated calcium carbonate ranged from $0.1{\mu}m$ to $80{\mu}m$. But, the average particle size of cell wall micropore loaded calcium carbonate was $4{\mu}m$. The paper made from never dried pulp fibers, the cell wall micropores which were filled with calcium carbonate, had better mechanical and optical properties than those of conventionally loaded or lumen loaded pulp fibers.

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Mechanical Properties and Reaction Products of Activated Slag System Depending on Gypsum Presence and Calcium Carbonate Addition (석고 존재 및 탄산칼슘 첨가에 따른 활성 슬래그의 역학적 성능 및 반응생성물)

  • Jeong, Yeonung;Lim, Gwi Hwan;Park, Su Hyeon;Kim, Joo Hyung;Kim, Tae-Sang
    • Journal of the Korea institute for structural maintenance and inspection
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    • v.24 no.4
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    • pp.55-63
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    • 2020
  • This study investigates the mechanical properties and reaction products of activated slag pastes depending on gypsum presence and calcium carbonate addition in terms of compressive strength tests and synchrotron X-ray diffraction. The chemicals of CaO and NaOH are used as activators with different two dosages. The reaction of CaO-activated slag without gypsum just accelerated by addition of calcium carbonate at early ages, but no improvement was observed at later ages. On the other hand, the mechanical properties of CaO-activated slag pastes with gypsum were improved with calcium carbonate, enhancing the stability of ettringite. The variation of mechanical properties of NaOH-activated slag pastes was negligible depending on calcium carbonate addition in case of no gypsum. The addition of calcium carbonate into NaOH-activated slag pastes with gypsum deteriorated its mechanical properties due to the ion competition between CO32- ions and SO32- ions, decreasing crystallinity of reaction products.

Studios on the Various Filters for Rubber Compounds. Part 1. Physical Properties of Domestic Calcium Carbonate for NR Compounds (고무용(用) 국산(國産) 각종충전제(各種充塡劑)에 관(關)한 연구(硏究) (제1보(第1報)) 고무용(用) 국산(國産) 탄산(炭酸)칼슘의 성능(性能)에 관(關)하여)

  • Lee, Myung-Whan;An, Young-Pil
    • Elastomers and Composites
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    • v.5 no.1
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    • pp.69-74
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    • 1970
  • The influence of various calcium carbonate on the physical properties of natural rubber have teen carries out extensive experiments on compounding. Final evaluation was made through various kinds of physical test-tensile strength, modulus, tear strength and hardnees-including particle size. The results are as follows: 1. Generally, tile tensile strength, modulus and tear strength showed the similar tendency in various calcium carbonate compounding. 2. The maximum volume of general using have been obtained with 150 phr calcium carbonate in $NR-CaCO_3$ compounding. 3. The particle size of domestic calcium carbonate showed $1.0\mu-2.6\mu$.

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Morphological and Physical Properties of ONP Treated by CaCO3 In-situ Precipitation Method (탄산칼슘 in-situ precipitation 처리된 신문고지의 형태와 물성변화)

  • Lee, Young Ho;Jung, Jae Kwon;Lee, Ki Seung;Seo, Yung Bum
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.45 no.6
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    • pp.44-54
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    • 2013
  • Replacing OMG (old magazine) to ONP (old newspaper) by raising optical property through $CaCO_3$ in-situ precipitation method in white duplex board presents cost reduction and possible drying energy saving. The strength property impairment by the presence of $CaCO_3$ could be supplemented by the fiber furnish treatment or strength polymer addition. In $CaCO_3$ in-situ precipitation of ONP, it was found from morphological study using FlowCAM, an image analyzer, that most of calcium carbonate were formed on the fines, and made the size of the fines larger. For the case of forming calcium carbonate only on the fractionated fines, the size of the fines were the biggest, and there were more clean surface areas available for bonding for the fractionated long fibers when fractionated fibers and fines were regrouped to make paper.

Effect of Surface Modification of Calcium Carbonate Nanoparticles by Octyltrimethoxysilane on the Stability of Emulsion and Foam (실란 커플링제 옥틸트리메톡시실란에 의해 표면 개질된 탄산칼슘 나노입자가 에멀젼 및 기포 안정성에 미치는 영향)

  • Lim, Jong Choo;Park, Ki Ho;Lee, Jeong Min;Shin, Hee Dong
    • Applied Chemistry for Engineering
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    • v.33 no.4
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    • pp.386-393
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    • 2022
  • In this study, the surface modification of calcium carbonate (CaCO3) nanoparticles by a silane coupling agent, octyltrimethoxysilane (OTMS), was investigated and characterized using Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) analysis. Both floating tests and contact angle measurements were also conducted to study the effect of OTMS concentration on the hydrophobicity of CaCO3 nanoparticles. It was found that the active ratio for the CaCO3 nanoparticles modified by 1 wt% of OTMS was 97.0 ± 0.5%, indicating that OTMS is a very effective silane coupling agent in enhancing the hydrophobicity of the CaCO3 nanoparticle surface. The most stable foam was generated with 1 wt% of CaCO3 nanoparticles in aqueous solutions at 1 wt% of OTMS, where the contact angle of water was found to be 91.8 ± 0.7°. It was also found that the most stable emulsion drops were formed at the same OTMS concentration. These results suggest that CaCO3 nanoparticles modified by a silane coupling agent OTMS are a powerful candidate for a foam stabilizer or an emulsifier in many industrial applications.