• Title/Summary/Keyword: calcium-carbonate

Search Result 761, Processing Time 0.028 seconds

Formation and Control of Calcium Carbonate Films having Aragonite Crystal Structure by Electro-Chemical Process (전기화학적 프로세스에 의한 아라고나이트 결정구조 탄산칼슘 막의 형성 및 제어)

  • Lee, Seung-Hyo;Lee, Myeong-Hoon
    • Journal of the Korean institute of surface engineering
    • /
    • v.51 no.5
    • /
    • pp.325-331
    • /
    • 2018
  • Calcium carbonate($CaCO_3$) films were formed by an eco-friendly electro-chemical technique on steel substrates in synthesized distilled water solutions containing $NaHCO_3$, $CaCl_2$ and $MgCl_2$ with different ratio respectively. It was investigated to confirm the effect of $Mg^{2+}$ concentration by Scanning Electron Microscopy(SEM), Energy Dispersive x-ray Spectroscopy(EDS) and X-Ray Diffraction(XRD) respectively. From an experimental result, only calcite crystals were found in solution containing no $Mg^{2+}$. By increasing concentration of $Mg^{2+}$, deposition rate decreased and crystal structure was transformed form calcite to aragonite. In case of including $MgCl_2$ 300mM in synthesized solutions containing $NaHCO_3$, $CaCl_2$ 60mM, it was showed over the 90% of aragonite contents which have quite high deposition rate of aragonite. Also, it was confirmed that $Mg^{2+}$ acted as inhibitor on the films which made transforming from calcite to aragonite.

Phase Changes of Calcium Carbonate by Temperature and RPM in Continuous Crystallizer (연속식 결정화기에서 온도와 교반속도에 의한 탄산칼슘 결정의 형상변화)

  • Shin, Yuonjeong;Han, Hyunkak
    • Korean Chemical Engineering Research
    • /
    • v.57 no.5
    • /
    • pp.666-671
    • /
    • 2019
  • Calcium carbonate involves three phases such as calcite, vaterite, and aragonite. Calcite and aragonite were more thermodynamically stable than vaterite. The synthesis of aragonite crystals by the reaction with sodium carbonate and calcium chloride solutions was investigated focusing on the effect of temperature and rpm in continuous crystallizer. In the batch crystallization test, calcite was synthesized by a relatively low temperature (under $40^{\circ}C$), but aragonite was formed at high temperature. In the continuous process with 100 rpm, no aragonite was found regardless of reaction temperature. But as increasing the stirring rate to 300 rpm and 500 rpm, the ratio of aragonite to calcite increased as increasing the temperature.

Formation Characteristics of Precipitated Calcium Carbonate by Carbonation Process

  • Kim, Chiho;Seok, Mingwang;Kim, Yangdo
    • Korean Journal of Materials Research
    • /
    • v.31 no.1
    • /
    • pp.1-7
    • /
    • 2021
  • The characteristics and morphology of precipitated calcium carbonate (PCC) particles produced by carbonation process with various experimental conditions are investigated in this study. The crystal structures of PCC formed by carbonation process are calcite and aragonite. The crystal structure of PCC particles synthesized without adipic acid additive is calcite only, regardless of the reaction temperature. Needle-like shape aragonite phase started to form at reactor temperature of 80℃ with the adipic acid additive. Particle size of the single phase calcite PCC synthesized without adipic acid additive is about 1 ~ 3 ㎛, with homogenous distribution. The aragonite PCC also shows uniform size distribution. The reaction temperature and concentration of adipic acid additive do not show any significant effects on the particle size distribution. Aragonite phase grown to a large aspect ratio of needle-like shape showed relatively improved whiteness. The measured whiteness value of single calcite phase is about 95.95, while that of the mixture of calcite and aragonite is about 99.11.

A STUDY ON THE SHEAR BOND STRENGTH OF LUTING GLASS IONOMER AND DENTIN TREATED WITH CALCIUM SOLUTION (칼슘수용액으로 처리한 상아질과 합착용 글래스아이오노머의 전단결합강도에 관한 연구)

  • Paik, Young-Girl;Lee, Sung-Bok;Park, Nam-Soo
    • The Journal of Korean Academy of Prosthodontics
    • /
    • v.34 no.3
    • /
    • pp.593-610
    • /
    • 1996
  • The objective of this paper was to evaluate the shear bond strength of luting glass ionomer cement with defferent calcium based solution treatment on dentin surface. 120 extracted human teeth were classified into 12 group based on presence of smear layer on dentin surface and type of treatment solution. Smear layer remove on dentin surface was done using 6% citric acid for 60 seconds. Five different dentin surface treatment solutions(calcium acetate, calcium carbonate, clacium chlorided, calcium hydroxide, and calcium phosphate) were evaluated in this study. After surface modification, metal ring(inner diameter : 3mm, depth : 1mm) was placed to expose the same dentin surface area and inner space was filled with luting glass ionomer cement according to the recommended procedure for stadard clinical procedure. The shear bond strength of glass ionomer cement was determined after 24 hours. SEM was used for the evaluation of the surface morphologic changes and EDAX analysis was done for determination of the change of the calcium contents of treated dentin. Follwing conclusion can be drawn : 1. In the group of the dentin surface with smear layer, the calcium carbonate solution was the most effective for the increase of the clacium content and the shear bond strength of glass ionomer cement to dentin surfaces. 2. In the group of the calcium carbonate treated dentin with msear layer, the shear bond strength was increased twice compared to the control group and cohesive failure mode was observed. 3. The shear bond strength of cement was increased significantly be the removal of smear layer using 6% citric aicd. However, additional calcium solution treatments were not effective for further bond strength increase. 4. The shear bond strength of cement was significantly improved by both of the removal of smear layer and the calcium solution treatment, and the former was more effective for bond strength improvement. 5. The smear layer removed/calcium solution treated groups showed dentinal tubule obstruction and crystal attachment in SEM evaluation. However, the shear bond strengths of these groups were not increased compared to the smear layer removed/no dentin treatment group.

  • PDF

Evaluation on the Aggressivity of Drinking Water for Corrosion Control in Water Distribution System (상수도관로의 부식 방지를 위한 수돗물의 침식성 평가)

  • Kwak, Phill-Jae;Lee, Hyun-Dong;Nam, Sang-Ho
    • Journal of Korean Society of Water and Wastewater
    • /
    • v.11 no.1
    • /
    • pp.53-63
    • /
    • 1997
  • The corrosion problems in water distribution system are reduced by decreasing the agressivity of drinking water which is evaluated by marble test and saturation indices(LSI or CCPP etc.). Marble test is a reliable method to determine the actual saturation condition of treated water. This study was done to determined the aggressivity of tap water and the effectiveness of $Ca(OH)_2$ and NaOH dosage for corrosion control. The drinking water in Seoul were evaluated by marble test and Langelier Index(LSI) and Calcium Carbonate Precipitation Potential(CCPP). The results indicated that the drinking water in Seoul were undersaturated as Calcium Carbonate($CaCO_3$). The LSI and CCPP of the water treated with $Ca(OH)_2$ were higher than that of water treated with NaOH. Therefore, to increase the Alkalinity and Calcium Hardness for corrosion control in water distribution system, $Ca(OH)_2$ is more effective than NaOH.

  • PDF

Fundamental Study on the CO2 fixation method using the Cement-saturated solution (시멘트 수용액을 이용한 CO2 고정화 방안에 관한 기초적 연구)

  • Kwack, Jae-Seok;Kang, Chang-Soo;Ahn, Hee-Sung;Lee, Han-Seung
    • Proceedings of the Korean Institute of Building Construction Conference
    • /
    • 2011.11a
    • /
    • pp.41-42
    • /
    • 2011
  • The purpose of this study is not only fixation of carbon dioxide using the cement-saturated solution by wet carbonating reaction but also evaluate the possibility of storage technology of Carbon dioxide. wet carbonation is reaction of CO2 injection by CO2 reactor. As a result of experiment, the carbon dioxide is fixed, and high-purity Calcium Carbonate is eluted.

  • PDF

Control of scale formation using high voltage impulse (고전압 임펄스에 의한 스케일 제어)

  • Yang, Seon-Hee;Chang, In-Soung
    • Journal of the Korea Academia-Industrial cooperation Society
    • /
    • v.16 no.3
    • /
    • pp.2301-2307
    • /
    • 2015
  • The aim of this study was to evaluate the feasibility of application of the high voltage impulse (HVI) technique to the control of scale formation by calcium carbonate, which is pointed out as an important issue in industrial water treatment. The HVI system consisted of the power supply, high voltage generator, capacitors, switch and impulse generator was designed and made in laboratory scale, which can make 17kV impulse. HVI was introduced to the reactor that was filled with synthetic water containing $Ca^{2+}$ion. The concentration of calcium ion decreased only 3.0% after 5 minutes of contact time. However, it decreased up to 13.7% after 60 minutes of HVI contact time. Temperature and pH increased but conductivity decreased due to precipitation of the calcium carbonate. Although the decrease in concentration of calcium ion was not sufficient, it was verified that the HVI technique could be applicable for the softening and desalting processes.

The Effects of Builders on Calcium Deposition on the Fabric (세척시 조제의 종류가 직물에의 Calcium 침착에 미치는 영향)

  • Park Moon He;Kahng Hewon;Kim Sung Reon
    • Journal of the Korean Society of Clothing and Textiles
    • /
    • v.6 no.1
    • /
    • pp.9-15
    • /
    • 1982
  • The influence of builders on calcium deposition on the fabric was studied by laundering the cotton fabric with sodium carbonate, sodium metasilicate, sodium tripolyphosphate and built detergents in hard water. The laundry variables were: 1) Washing cycles: 5, 10, 20, 30 and 40 cycles. 2) Water hardness: 100 ppm, 150 ppm, 200 ppm and 300 ppm. 3) Builders: $Na_2\;CO_3,\;Na_2\;SiO_3$ and STPP. 4) Detergents: Na-DBS, $Na-DBS+Na_2CO_3,\;Na-DBS+Na_2\;SiO_3,\;Na-DBS+STPP,\;Na-DBS+Na_2\;CO_3+STPP$, and $Na-DBS+Na_2\;SiO_3+STPP$. The fabric was washed for 15 minutes at 23+$1^{\circ}C$ in a washing machine(Gold Star WP 3007) under the similar condition with those of home laundering, and rinsed 3 times in the same water hardness for 5 minutes. The calcium deposits on the fabric was determined by EDTA-BACK titration methods. The results of this study were as follows: 1) The amount of calcium deposits on the fabric was increased with increasing wash cycles. This deposit was due to the build up of insoluble calcium carbonate. 2) As the water hardness increased, the amount of calcium deposits on the fabric was increased. 3) Alkaline builders, such as, $Na_2CO_3$ and $Na_2SiO_3$, promoted calcium deposition on the fabric, however STPP prevented calcium deposition on the fabric. 4) Fabric laundered with $Na-DBS+Na_2CO_3$ showed the highest calcium deposits on the fabric, and decreased with the order of $Na_2CO_3$, $Na-DBS+Na_2SiO_3$, and Na-DBS. And fabrics washed with phosphate-built detergents showed a small amount of calcium deposition.

  • PDF

Formation and Crystallization of Amorphous Calcium Carbonate in $Ca(OH)_2-H_2O-CO_2$ system ($Ca(OH)_2-H_2O-CO_2$계에서의 비정질 탄산칼슘 생서 및 결정화 연구)

  • 안지환;박찬훈
    • Resources Recycling
    • /
    • v.5 no.1
    • /
    • pp.42-49
    • /
    • 1996
  • The synthesis or amorphous calc~um carbonale in the reacllons oi cslcn~m hydroxide suspension - CO1 systcni !\.;is studied by uslng rneasulemel~ts of eleclrical conductivity, x-ray diftractorneter and t~ansmission eleclron microscope. The m~tial product of reactious was noncrystalline shape oI amorphous calcium carbo~iale confirmed by x-ray diffraction analyses. The amorphous calcium carbonate covered lhc surlace of calcium hydroxldc grains. Tlic electrical conductivity of suspension dec~eascd dramatically when the amorphous calcium carhonate was synlliesizcd. A portion or the amorplious calcmm carbonale clia~iged ilito [he chain calcite as an intermcdrate product. Thc continuo~~cso nrluctivity measurements of suspension were ahle to delennine the starting point of the synthesis and the mechallism of carbonation process

  • PDF

Clay adsorptive membranes for chromium removal from water

  • Kashaninia, Fatemeh;Rezaie, Hamid Reza;Sarpoolaky, Hossein
    • Membrane and Water Treatment
    • /
    • v.10 no.4
    • /
    • pp.259-264
    • /
    • 2019
  • Cost effective clay adsorptive microfiltration membranes were synthesized to remove Cr (III) from high polluted water. Raw and calcined bentonite were mixed in order to decrease the shrinkage and also increase the porosity; then, 20 wt% of carbonate was added and the samples, named B (without carbonate) and B-Ca20 (with 20 wt% calcium carbonate) were uniaxially pressed and after sufficient drying, fired at $1100^{\circ}C$ for 3 hours. Then, physical and mechanical properties of the samples, their phase analyses and microstructure and also their ability for Cr(III) removal from high polluted water (including 1000 ppm Cr (III) ions) were studied. Results showed that the addition of calcium carbonate lead the porosity to increase to 33.5% while contrary to organic pore formers like starch, due to the formation of wollastonite, the mechanical strength not only didn't collapse but also improved to 36.77 MPa. Besides, sample B-Ca20, due to the presence of wollastonite and anorthite, could remove 99.97% of Cr (III) ions. Hence, a very economic and cost effective combination of membrane filtration and adsorption technology was achieved for water treatment which made microfiltration membranes act even better than nanofiltration ones without using any adsorptive nano particles.