• Title/Summary/Keyword: Calcium Carbonate(CaCO3)

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Variation of Calcium Carbonate Content and Dansgaard-Oeschger Events in the Continental Slope of the Central Bering Sea during the Last 65 Kyr (베링해 중부 대륙사면 지역의 지난 65,000년 동안 탄산염 함량 변화와 Dansgaard-Oeschger 사건들)

  • Kim, Sung-Han;Khim, Boo-Keun;Itaki, Takuya;Shin, Hye-Sun
    • Ocean and Polar Research
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    • v.30 no.3
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    • pp.215-224
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    • 2008
  • A piston core (MR06-04 PC23A) collected from the northern continental slope in the central Bering Sea has recorded the high-resolution millennial-scale variation of calcium carbonate ($CaCO3$) content during the last 65 kyr. An estimation of the age of the core sediments was carried out by using the lithologic correlation of the deglacial laminated layers with a neighboring core (HLY02023JPC), complementing the last appearance datum of both Lychnocanoma nipponica sakaii (54 kyr) and Amphimelissa setosa (85 kyr). The probable age of core MR06-04 PC23A was approximately younger than 65 kyr. Two distinct events of a significant increase of $CaCO3$ in the deglacial laminated sediments clearly correspond to MWP1A and MWP1B in the Bering Sea (Gorbarenko et al. 2005) and to T1ANP and T1BNP in the North Pacific (Gorbarenko 1996). These pronounced peaks of $CaCO3$ contents result from the elevated carbonate production in the surface water and the subsequent weakened dilution due to terrestrial input, along with an enhanced oxygen minimum zone. The $CaCO3$ contents are low (${\sim}2%$) during the last glacial period mainly because of a low carbonate production caused by an expanded sea-ice cover and an increased dilution by terrigenous particles due to their closer distance to the continent during the sea-level low stand. The occurrence of seven distinct $CaCO3$ peaks in core MR06-04 PC23A is remarkable during MIS 3 and MIS 4, and they most likely correlate to the short-term millennial Dansgaard-Oeschger events.

Study on the Dispersion Stability of Precipitated Calcium Carbonate Suspensions (침강성 탄산칼슘 현탁액의 분산 안정성에 관한 연구)

  • Park, Myung-Jae;Ahn, Ji-Whan;Kim, Hwan
    • Journal of the Korean Ceramic Society
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    • v.38 no.4
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    • pp.343-350
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    • 2001
  • 본 연구에서는 탄산화법으로 침강성 CaCO$_3$분말을 제조하고 제조된 CaCO$_3$현탁액의 분산안정성을 연구하였다. CaCO$_3$현탁액의 pH 변화와 고분자전해질 PMAA와 PAA의 첨가에 따른 입자크기, 유동학적 특성(점도), zeta potential 및 현탁액의 침강속도 등을 측정하였다. 탄산화법에 의해 약 0.1$\mu\textrm{m}$ 크기와 비표면적이 23.57$m^2$/g인 단분단 calcite형 CaCO$_3$분말을 제조하였다. pH가 11인 CaCO$_3$현탁액에 0.01 wt% PMAA가 첨가된 경우에 우수한 분산안정성을 나타내었는데 이는 CaCO$_3$입자표면에 PMAA의 흡착에 의한 electrosteric 안정화기구와 CaCO$_3$입자들 사이의 정전기적 반발력에 의한 것으로 판단된다. PMAA와 PAA 첨가량 변화에 따른 pH 6, 9, 11의 CaCO$_3$현탁액의 침전높이를 측정한 결과 PMAA와 PAA의 농도가 0.15 wt% 부근에서 분산안정성을 보였는데 이는 CaCO$_3$입자들 사이간의 분산제에 의한 뚜렷한 경계를 갖는 흡착층이 형성되었기 때문으로 생각되며 따라서 CaCO$_3$현탁액의 최적 분산안정성을 위해서는 적절한 pH 조절과 PMAA 및 PAA의 첨가가 필요함을 알 수 있다.

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Variation Calcium Carbonate Content in Deep-Sea Pelagic Sediments of the Western Pacific Ocean (서태평양 심해 원양성 퇴적물의 탄산염 함량 변화)

  • Khim, Boo-Keun;Kim, Yeo-Hun;Kim, Hyung-Jeek;Hyeong, Ki-Seong;Yoo, Chan-Min
    • Ocean and Polar Research
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    • v.32 no.1
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    • pp.15-22
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    • 2010
  • Calcium carbonate ($CaCO_3$) content was measured from 3 box core (BC060301, BC060303, BC070301) sediments, in addition to pilot core (PC313) sediments, from deep waters within the Western Pacific Ocean. At the two collection sites (BC060301, PC313) located close to the equator, downcore variation exhibited low $CaCO_3$ content during the interglacial period and high $CaCO_3$ content during the glacial period. Variation of coarse fraction (>$63\;{\mu}m$) content also followed changes in $CaCO_3$ content, indicating that dissolution effect of bottom water decreased during the glacial period. Such variation pattern is typical of the Pacific Ocean. However, downcore variation at the two collection sites (BC060303, BC070301) in the Philippine Sea contrasted the trend of the previous two cores (i.e., high $CaCO_3$ content during the interglacial period and low during the glacial period). This pattern is typical of the Atlantic Ocean. Such results may be attributed to the increasing dilution effect, initiated possibly by the increased transportation of terrigenous materials from nearby continent and archipelago during the glacial period when sea level was low. Alternatively, it is possible that the non-carbonate biogenic particles may have been responsible for dilution. Because of these uncertainties, the record of $CaCO_3$ variation in the deep Western Pacific Ocean is not regionally consistent.

Properties of Polypropylene/CaCO3 Composites from the Shape of Calcium Carbonate (Polypropylene/CaCO3 복합재료에 있어서 입자 형태에 따른 물성)

  • Lyu, S.G.;Bae, K.S.;Sur, G.S.
    • Applied Chemistry for Engineering
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    • v.8 no.5
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    • pp.771-776
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    • 1997
  • The various shape of calcium carbonate were prepared. For the preparation of the PP/$CaCO_3$ composite, these synthetic calcium carbonate(cubic, spheric and neddle type) and PP were mixed on a two roll mill and the mixture were pressed into plate. The effect of particle shape in the prepared composite on the crystallization temperature, heat of fusion, size of spherulite and mechanical properities were investigated. It was found that the former four were strongly influenced by that. When, especially, vaterite was mixed with PP, the size of spherulite was smaller and the degree of crystallinity was higher than others. Therefore, the tensile strength and Young's modulus were higher.

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Extraction of Precipitated Calcium Carbonate from Oyster Shell waste and Its Applications

  • Ramakrishna, Chilakala;Thenepalli, Thriveni;Nam, Seong Young;Kim, Chunsik;Ahn, Ji Whan
    • Journal of Energy Engineering
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    • v.27 no.1
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    • pp.51-58
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    • 2018
  • In this paper, we reported that the influence of advanced functional mineral filler calcium carbonate ($CaCO_3$) extracted from oyster shell waste, which are rich mineral sources of $CaCO_3$. Oyster Shells, available in abundance, have no eminent use and are commonly regarded as waste. Their improper disposal causes a significant level of environmental concern and also results in a waste of natural resources. Recycling shell waste could potentially eliminate the disposal problem, and also turn an otherwise useless waste into high value added products. Oyster shell waste calcination process to produce pure lime (CaO) which have good anti-microbial property for waste water treatment and then focuses on its current applications to treat the coffee waste and its effluents for biological treatment and utilization as a fertilizers.

Complete Genome and Calcium Carbonate Precipitation of Alkaliphilic Bacillus sp. AK13 for Self-Healing Concrete

  • Jung, Yoonhee;Kim, Wonjae;Kim, Wook;Park, Woojun
    • Journal of Microbiology and Biotechnology
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    • v.30 no.3
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    • pp.404-416
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    • 2020
  • Bacteria that are resistant to high temperatures and alkaline environments are essential for the biological repair of damaged concrete. Alkaliphilic and halotolerant Bacillus sp. AK13 was isolated from the rhizosphere of Miscanthus sacchariflorus. Unlike other tested Bacillus species, the AK13 strain grows at pH 13 and withstands 11% (w/v) NaCl. Growth of the AK13 strain at elevated pH without urea promoted calcium carbonate (CaCO3) formation. Irregular vaterite-like CaCO3 minerals that were tightly attached to cells were observed using field-emission scanning electron microscopy. Energy-dispersive X-ray spectrometry, confocal laser scanning microscopy, and X-ray diffraction analyses confirmed the presence of CaCO3 around the cell. Isotope ration mass spectrometry analysis confirmed that the majority of CO32- ions in the CaCO3 were produced by cellular respiration rather than being derived from atmospheric carbon dioxide. The minerals produced from calcium acetate-added growth medium formed smaller crystals than those formed in calcium lactate-added medium. Strain AK13 appears to heal cracks on mortar specimens when applied as a pelletized spore powder. Alkaliphilic Bacillus sp. AK13 is a promising candidate for self-healing agents in concrete.

Shipboard Verification Test of Onboard Carbon Dioxide Capture System (OCCS) Using Sodium Hydroxide(NaOH) Solution (가성소다(NaOH) 용액을 이용한 선상 이산화탄소 포집 장치의 선박 검증시험)

  • Gwang Hyun Lee;Hyung Ju Roh;Min woo Lee;Won Kyeong Son;Jae Yeoul Jeong;Tae-Hong Kim;Byung-Tak NAM;Jae-Ik Kim
    • Journal of the Society of Naval Architects of Korea
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    • v.61 no.1
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    • pp.51-60
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    • 2024
  • Hi Air Korea and Hanwha ocean are currently developing an Onboard Carbon dioxide Capture System (OCCS) to absorb CO2 emitted from ship's engine using a sodium hydroxide(NaOH) solution, and converting the resulting salt into a solid form through a chemical reaction with calcium oxide (CaO). The system process involves the following steps; 1)The reaction of CO2 gas absorption in water, 2)The reaction between carbonic acid (H2CO3) and NaOH solution to produce carbonate or bicarbonate, and 3)The reaction between carbonate or bicarbonate and CaO to form calcium carbonate (CaCO3). And ultimately, the solid material, CaCO3, is separated and discharged using a separator. The OCCS has been installed on an ship and the test results have confirmed significant reduction effects of CO2 in the ship's exhaust gas. A portion of the exhaust gas emitted from the engine was transferred to the OCCS using a blower. The flow rate of the transferred gas ranged from 800 to 1384 m3/hr, and the CO2 concentration in the exhaust gas was 5.1 vol% for VLSFO, 3.7 vol% for LNG and a 12 wt% NaOH solution was used. The results showed a CO2 capture efficiency of approximately 42.5 to 64.1 vol% and the CO2 capture rate approximately 48.4 to 52.2kg/hr. Additionally, to assess the impact of the discharged CaCO3on the marine ecosystem, we conducted "marine ecotoxicity test" and performed Computational Fluid Dynamics (CFD) analysis to evaluate the dispersion and dilution of the discharged effluent.

Review of Water-Based Synthetic Methods of Calcium Carbonate Polymorphs and Their Morphological Features (탄산칼슘 동질이상체의 수용액 기반 합성법 및 형태학적 특성 리뷰)

  • YoungJae Kim;Seon Yong Lee;Young Jae Lee
    • Economic and Environmental Geology
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    • v.56 no.3
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    • pp.217-227
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    • 2023
  • Crystalline calcium carbonate (CaCO3) occurs in various geological and aqueous environments as calcite, aragonite, and vaterite. These minerals also have practical applications in engineered settings. Synthetic methods of calcium carbonate have been developed for scientific research and technical applications. For example, these methods have become widely adopted for studying the formation of CaCO3 minerals and (geo-)chemical processes involving these minerals in natural and engineered systems. Furthermore, these methods have the potential to be applied in various technical and biomedical fields. Water-based synthesis is particularly important for simulating the formation of calcium carbonate minerals in natural aqueous environments. This review paper describes the procedures and experimental conditions for water-based synthetic methods of each calcium carbonate polymorph, compares the morphological and structural features of the resulting crystals, and analyzes the crystallization mechanisms.

Fundamental Characteristics of CO2-cured Mortar with Varied Rates of Blast Furnace Slag Fine Powder Substitution (고로슬래그 미분말 치환율에 따른 이산화탄소 양생 모르타르의 기초 물성)

  • Ryu, Ji-Su;Jang, Kyung-Su;Na, Hyeong-Won;Hyung, Won-Gil
    • Journal of the Korea Institute of Building Construction
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    • v.24 no.1
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    • pp.11-21
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    • 2024
  • This research elucidates the fundamental properties of carbon dioxide (CO2)-cured mortar as influenced by varying substitution rates of blast furnace slag fine powder. The findings indicate that CO2 curing enhances the formation of calcium carbonate (CaCO3), contributing to pore reduction and the early development of strength. While calcium hydroxide (Ca(OH)2) plays a more pivotal role in the primary development of strength compared to CaCO3, an increase in the substitution rate of blast furnace slag fine powder results in reduced production of Ca(OH)2. Nonetheless, the maintenance of strength through CaCO3 formation is observed even after the depletion of Ca(OH)2, suggesting that the required performance can be sustained post-exposure to the atmosphere following CO2 curing. It is noted that substitution rates exceeding 50% lead to performance deterioration due to CO2, highlighting the necessity for careful adjustment of the substitution ratio.

Recycling of Wastepaper(V): -Calcium Hardness Control of Process Water for Zero-Discharge System- (고지재상연구 (제5보) -공정수 폐쇄화를 위한 칼슘경도 조절-)

  • 지경락;류정용;신종호;송봉근;오세균
    • Journal of Korea Technical Association of The Pulp and Paper Industry
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    • v.31 no.2
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    • pp.15-24
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    • 1999
  • A new technique for recycling of white water was developed in order to reduce the calcium hardness in a closed OCC recycling system. Calcium ions present in the white water were precipitated as calcium carbonate by reacting with sodium carbonate, and the precipitated $CaCO_3$ was removed from the system using a flotation fractionation method, which has been commonly used in deinking process. In the flotation stage, a mixed gas of $CO_2$-air was purged into the flotation cell because the pH of $Na_2CO_3$-treated white water was reduced to neutral by $CO_2$ gas. Since $CaCO_3$ precipitate tends to stick onto fine fiber surface and then selectively removed from the white water, a proper amount of suspended solid in white water acts as an important factor for deciding the removal efficiency. By the application of $Na_2CO_3$ addition-$CO_2$ flotation to the short circulated white water, the calcium hardness was significantly reduced by 87% and more. Removal of calcium ions with fine fibers led to a drainage improvement, reduction of fresh water consumption, and enhanced efficiency of wet-end chemicals.

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