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Academic literature on the topic 'Solid solution C2S–C3P'
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Journal articles on the topic "Solid solution C2S–C3P"
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Teratoko, Takuya, Nobuhiro Maruoka, Hiroyuki Shibata, and Shin-ya Kitamura. "Dissolution Behavior of Dicalcium Silicate and Tricalcium Phosphate Solid Solution and other Phases of Steelmaking Slag in an Aqueous Solution." High Temperature Materials and Processes 31, no. 4-5 (October 30, 2012): 329–38. http://dx.doi.org/10.1515/htmp-2012-0032.
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AbstractMost of the phosphorus in slag forms a solid solution of dicalcium silicate (C2S) and tricalcium phosphate (C3P), and the process used to separate this solid solution from the matrix phase is the same technology used to separate P from other valuable elements such as Mn and Cr containing in the matrix phase. Although it is known that the solubility of C2S in an aqueous solution is much greater than that of C3P, the solubility of the solid solution and that of the matrix phase have yet to be investigated. To clarify the possibility of selectively extracting P from slag through a leaching process, the dissolution behaviors of the solid solution at various compositions and that of the matrix phase were investigated. The following results were obtained: The dissolution ratio of Ca to the aqueous solution at pH = 7 was close to 1.0 in the case of pure C2S and decreased greatly with increasing C3P content. The dissolution ratio of P was about 0.1 and did not change relative to the C3P content. When the ratio of C3P in the solid solution was higher than 0.3, hydroxyapatite (HAP) formation was observed in the residue. The dissolution ratio of P increased for 30 min, and after reaching the maximum value, started to decrease owing to the precipitation of HAP. The dissolution ratio of each element from a glassy slag sample (matrix phase) was lower than that from the solid solution at every pH level.In this study, the possibility to extract a solid solution containing P without dissolving the matrix phase was found through the use of an aqueous solution at pH = 7, although the dissolution ratio of P was not sufficiently high.
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Deng, Aijun, Yunjin Xia, Jie Li, and Dingdong Fan. "Effect of 2CaO·SiO2 particles addition on dephosphorization behavior." High Temperature Materials and Processes 39, no. 1 (June 30, 2020): 219–27. http://dx.doi.org/10.1515/htmp-2020-0066.
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AbstractThe effect of the addition of 2CaO·SiO2 solid particles on dephosphorization behavior in carbon-saturated hot metal was investigated. The research results showed that the addition of 2CaO·SiO2 particles have little influence on desilication and demanganization, and the removal of [Si] and [Mn] occurred in the first 5 min with different conditions where the contents of 2CaO·SiO2 particles addition for the conditions 1, 2, 3, 4, and 5 are 0, 2.2, 6.4, 8.6, and 13.0 g, respectively. The final dephosphorization ratios for the conditions 1, 2, 3, 4, and 5 are 61.2%, 66.9%, 79.6%, 63.0%, and 78.1%, respectively. The dephosphorization ratio decreases with the increase of 2CaO·SiO2 particles in the first 3 min. The reason for this is that the dephosphorization process between hot metal and slag containing C2S phase consisted of two stages: Stage 1, [P] transfers from hot metal to liquid slag and Stage 2, the dephosphorization production (3CaO·P2O5) in liquid slag reacts with 2CaO·SiO2 to form C2S–C3P solid solution. The increase of 2CaO·SiO2 particles increases the viscosity of slag and weakens the dephosphorization ability of the stage 1. The SEM and XRD analyses show that the phase of dephosphorization slag with the addition of different 2CaO·SiO2 particles is composed of white RO phase, complex liquid silicate phase, and black solid phase (C2S or C2S–C3P). Because the contents of C2S–C3P and 2CaO·SiO2 in slag and the dephosphorization ability of the two stages are different, the dephosphorization ability with different conditions is different.
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Liu, Shi-Wei, Ping-Ping Li, Chuan-Ming Du, and Ning-Ning Lv. "Effect of Fe2O3 Content and Acid on the Leaching Behavior of Phosphorus from Dephosphorization Slag." Minerals 11, no. 9 (September 7, 2021): 972. http://dx.doi.org/10.3390/min11090972.
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Dephosphorization slag contains considerable quantities of valuable components, such as P2O5 and FeOx. To recover P from dephosphorization slag, selective leaching has been adopted to separate the P-concentrating mineral phase. In this study, the effect of Fe2O3 content in slag and acid on the leaching behavior of P from dephosphorization slag was investigated. It was found that a higher Fe2O3 content in slag resulted in a higher P2O5 content in the C2S–C3P solid solution. Increasing the Fe2O3 content in slag promoted the dissolution of P and simultaneously suppressed the dissolution of other elements, facilitating the selective leaching of P. In the hydrochloric acid solution, more than 81% of P could be dissolved from dephosphorization slag at pH 4, and the dissolution ratio of Fe was nearly zero, achieving excellent selective leaching. Although better selective leaching was also realized in the citric acid solution at pH 5, hydrochloric acid was considered the appropriate leaching agent from the perspective of leaching cost. Through selective leaching, almost all the C2S–C3P solid solution was dissolved from dephosphorization slag, and the Fe-bearing matrix phase and magnesioferrite remained in the residue. The residue with low P2O5 content can be reutilized in ironmaking or steelmaking processes.
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Liu, Jinyan, Cheng Yi, Hongguang Zhu, and Hongqiang Ma. "Property Comparison of Alkali-Activated Carbon Steel Slag (CSS) and Stainless Steel Slag (SSS) and Role of Blast Furnace Slag (BFS) Chemical Composition." Materials 12, no. 20 (October 11, 2019): 3307. http://dx.doi.org/10.3390/ma12203307.
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In order to compare the properties of alkali-activated carbon steel slag (CSS) and stainless steel slag (SSS), the effects of sodium hydroxide/sodium silicate solution mass ratio (NH/NS), liquid/solid ratio and blast furnace slag (BFS) dosage on the compressive strength, hydration products and hydration degree of CSS and SSS were studied. Furthermore, a combination of X-ray diffraction (XRD), thermo-gravimetric analysis coupled with differential thermal analysis (TGA-DTA), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscope-energy dispersive spectrometer (SEM-EDS) were used to characterize the morphology and structure of alkali-activated CSS-BFS and SSS-BFS cementitious materials. As the results revealed, the primary hydrate of alkali-activated CSS and SSS is C-(A)-S-H with Q2 [SiO4] units, which has a low Ca/Si ratio and includes inert phases like a CaO-FeO-MnO-MgO solid solution (RO) in CSS while cuspidine, magnesiochromite etc. in SSS. More active C3S and β-C2S promote the alkali activation of CSS, whereas the less active γ-C2S hinders the depolymerization of SSS. The incorporation of BFS does not change the hydrate, whose seed effect is helpful for accelerating the depolymerization and polycondensation of CSS and SSS, especially for SSS, and makes the hydrate increase significantly. Owing to the high SiO2 and Al2O3 contents of SSS, the C-(A)-S-H chain length is increased, thus facilitating the polycondensation effect. In this study, the optimal NH/NS of CSS and SSS is NH/NS= 1:2, and the optimal liquid/solid ratio is 0.29. Compared to CSS–BFS, the C-(A)-S-H gel produced by SSS–BFS has lower Ca/Si and Al/Si ratios. Unlike CSS, pure SSS is inappropriate as an alkali-activated precursor and needs to be co-activated with BFS.
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Kang, Rui, Su Hua Ma, and Xiao Dong Shen. "Secondary Sintering Cement Clinker in SO2 Atmosphere: Composition and Structure Effects." Materials Science Forum 1036 (June 29, 2021): 208–13. http://dx.doi.org/10.4028/www.scientific.net/msf.1036.208.
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A gas-solid reaction method was adopted in this work to explore the influence of SO2 gas on the composition and structure of secondary sintering cement clinker. In this process, the Portland cement clinker was secondarily sintered at different temperatures and a mixed gas mixed with SO2 was introduced simultaneously in a tube furnace. X-ray powder diffraction (XRD) combined with rietveld refinement was used to determine the phase composition of the cement clinker and the corresponding phase content. The experimental results showed that the increase in temperature conduced to increasing the content of SO3 solid solution, C2S and CaO, but decreasing the C3S content. Moreover, as the ratio of SO3/MgO (by mass) increases, the content of M1-type alite also increased. And the result of hydration heat release was positively correlated with the content of alite in the clinker. If the content of alite was low, the heat flow was low, as well as the cumulative heat, and vice versa.
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Bouregba, Adil, Hassan Ez-Zaki, Abdeljebbar Diouri, and Omar Sassi. "β-Dicalcium Silicate Cement Modified with β-Tricalcium Phosphate: In Vitro Bioactivity and Mechanical Strength." Journal of Biomimetics, Biomaterials and Biomedical Engineering 35 (January 2018): 9–19. http://dx.doi.org/10.4028/www.scientific.net/jbbbe.35.9.
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Calcium-silicate cement mainly based on dicalcium-silicate (C2S) was synthesized by the mean of solid state reaction. Beta-C3P was added to C2S to obtain C2S-C3P. Zinc oxide and bismuth oxide was incorporated to prepare radioc cement. In this work, the bioactivity and the mechanical strength of the synthesized cement were investigated. The in vitro test was carried out by immersion of cement pastilles in the artificial saliva in different periods from 4 hours to 30 days. Whereas the mechanical strength of some samples was operated at 28 and 72 days. The specimens are characterized by X-ray diffraction , Infrared spectroscopy and scanning electron microscopy. The finding results indicated that hydroxyapatite may appear after 24 hours of soaking; it was also shown that the presence of C3P with a small amount of the cement can enhance the bioactivity and develop more resistance strength of cement. Moreover, the addition of zinc oxide and bismuth oxide increase the radiopacity of the cement. However, the mechanical strength enhances with the incorporation of the zinc oxide while decrease with bismuth oxide. It was concluded then that there is possibility of combining addition of C3P (10%) and an agent radiopacifiers ZnO/Bi2O3(15%) with small amounts on C2S to obtain a cement with excellent bioactivity, good mechanical strength and significante radiopacity that makes this material a great candidate as a biomaterial for biomedical use.
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Pritula, O., Lˇ Smrcˇok, and B. Baumgartner. "On reproducibility of Rietveld analysis of reference Portland cement clinkers." Powder Diffraction 18, no. 1 (March 2003): 16–22. http://dx.doi.org/10.1154/1.1545116.
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Weight fractions of four dominant phases (C3S, C2S, C4AF and C3A) present in the NIST Reference Portland clinkers 8486, 8487 and 8488 were estimated by a series of Rietveld refinements. Calculated powder patterns were derived from the structural data for monoclinic C3S and C2S, orthorhombic C4AF and cubic C3A. X-ray diffraction data were collected in two laboratories with two diffractometers, a reflection and a transmission one. There were no significant differences between the results of the refinements based on the data sets collected on the machines with different experimental arrangements. Estimated phase compositions were compared to the reference values found by optical microscopy (MPC). Median agreement between refined and reference values within ±5% (absolute) was found only for 8488 clinker; for 8486 and C3A-rich 8487 it was within ±10% (absolute). In the majority of the refinements numerical instabilities were detected, leading to large correlations between FWHM and temperature parameters of some phases. The results obtained for C4AF were probably influenced by the presence of possible solid solutions with the structures close to that of C4AF. Weight fractions of low abundant C3A were estimated with the largest relative errors reaching in several cases ∼100%.
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Hao, Ming, Caroline E. Pierotti, Sergey Tkachev, Vitali Prakapenka, and Jin S. Zhang. "The single-crystal elastic properties of the jadeite-diopside solid solution and their implications for the composition-dependent seismic properties of eclogite." American Mineralogist 104, no. 7 (July 1, 2019): 1016–21. http://dx.doi.org/10.2138/am-2019-6990.
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Abstract The 13 single-crystal adiabatic elastic moduli (Cij) of a C2/c jadeite sample close to the ideal composition (NaAlSi2O6) and a natural P2/n diopside-rich omphacite sample have been measured at ambient condition by Brillouin spectroscopy. The obtained Cij values for the jadeite sample are: C11 = 265.4(9) GPa, C22 = 247(1) GPa, C33 = 274(1) GPa, C44 = 85.8(7) GPa, C55 = 69.3(5) GPa, C66 = 93.0(7) GPa, C12 = 84(1) GPa, C13 = 66(1) GPa, C23 = 87(2) GPa, C15 = 5.4(7) GPa, C25 = 17(1) GPa, C35 = 28.7(6) GPa, C46 = 14.6(6) GPa. Voigt-Reuss-Hill averaging of the Cij values yields aggregate bulk modulus KS = 138(3) GPa and shear modulus G = 84(2) GPa for jadeite. Systematic analysis combing previous single-crystal elasticity measurements within the diopside-jadeite solid solution indicates that the linear trends are valid for most Cij values. The νp and νs of omphacite decrease with diopside content, though the velocity changes are small as diopside component exceeds 70%. We also found that both the isotropic νp and νs, as well as the seismic anisotropy of eclogite, changed strongly with the bulk-chemical composition. The relationship between the anisotropic velocities of eclogite and the chemical composition can be a useful tool to trace the origin of the eclogitic materials in the Earth's mantle.
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Rao, Lei, Yuanchi Dong, Mancheng Gui, Yaohui Zhang, Xingmei Shen, Xingrong Wu, and Fabin Cao. "Growth, Stratification, and Liberation of Phosphorus-Rich C2S in Modified BOF Steel Slag." Materials 13, no. 1 (January 3, 2020): 203. http://dx.doi.org/10.3390/ma13010203.
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Basic oxygen furnace (BOF) slag was modified by adding 3.5% SiO2 and holding at 1673 K for 0, 5, 40, 90, 240, or 360 min. Kilo-scale modification was also carried out. The growth, stratification, and liberation of P-rich C2S in the modified slag were investigated. The optimum holding time was 240 min, and 90% of C2S grains were above 30 μm in size. The phosphorus content increased with holding time, and after modification, the phosphorus content in C2S was nearly three times higher than that in the original slag (2.23%). Obvious stratification of C2S was observed in the kilo-scale modification. Upper C2S particles with a relatively larger size of 20–110 μm was independent of RO (FeO-MgO-MnO solid solution) and spinel, which is favorable for liberation. Lower C2S was less than 3 μm and was embedded in spinel, which is not conducive to liberation. The content of phosphorus in upper C2S (6.60%) was about twice that of the lower (3.80%). After grinding, most of the upper C2S existed as free particles and as locked particles in the lower. The liberation degree of C2S in the upper increased with grinding time, from 86.02% to 95.92% in the range of 30–300 s, and the optimum grinding time was 180 s. For the lower slag grinding for 300 s, the liberation degree of C2S was 40.07%.
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Lin, Lu, Yan-Ping Bao, Min Wang, and Xiang Li. "Effect of MgO and MnO on Phosphorus Utilization in P-Bearing Steelmaking Slag." High Temperature Materials and Processes 35, no. 4 (April 1, 2016): 425–32. http://dx.doi.org/10.1515/htmp-2014-0186.
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AbstractIn order to recycle the phosphorus in P-bearing converter slag and make it used as slag phosphate fertilizer, the effect of MgO and MnO in P-bearing steelmaking slag on phosphorus existence form, P2O5 solubility and magnetic separation behavior were researched systematically. The results show that the phosphorus in slag is mainly in the form of n2CaO · SiO2–3CaO · P2O5 (for short nC2S–C3P) solid solution in the P-rich phase for CaO-SiO2-FetO-P2O5-X (X stands for MgO and MnO, respectively). And the increasing of MgO and MnO content has no influence on precipitation of nC2S–C3P solid solution in slag, MnO and MgO mainly enter into RO phase and base phase to form MnFe2O4 and MgFe2O4, which has little effect on the P2O5 content of P-rich phase, so which has little effect on the degree of phosphorus enrichment and phosphorus occurrence form of the P-bearing slag. And adding MgO and MnO into CaO-SiO2-P2O5-Fe2O3 slag system can break the complex net structure formed by Si–O on certain degree, and also hinder the precipitation of β-Ca3(PO4)2 crystal with low citric acid solubility during the melting–cooling process. Therefore, adding appropriate MgO and MnO content into slag can improve the slag P2O5 solubility, but the effect of different amounts of MgO and MnO on the P2O5 solubility has little difference. Meanwhile, adding MgO and MnO into slag can improve the metallization of slag and magnetism of iron-rich phase, make the magnetic substances content increase and separation of phosphorus and iron incomplete, so it is adverse to phosphorus resources recovery from P-bearing slag by magnetic separation method. In order to recycle the phosphorus in P-bearing converter slag, the MgO and MnO content in the P-bearing slag should be controlled in the steelmaking process.
Dissertations / Theses on the topic "Solid solution C2S–C3P"
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Baráček, Jan. "Aplikace metody sol-gel na syntézu dikalciumsilikátu a jeho tuhých roztoků." Doctoral thesis, Vysoké učení technické v Brně. Fakulta chemická, 2014. http://www.nusl.cz/ntk/nusl-233387.
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The subject of this doctoral thesis was to elucidate the mechanism of reaction leading to the formation of dicalcium silicate (C2S), its solid solutions and other phosphatic calcium silicate phases using the sol-gel method of synthesis. SiO2 (Tosil A), CaO (calcium nitrate tetra-hydrate) and H3PO4 (as a source of P2O5) were used as starting materials. Series of samples with different content of P2O5 were synthesized. The characterization of Tosil A and samples was based on the following methods: DTA/TGA and EGA, XRD and SEM and EDS analy-ses. It is known, that phosphorous oxide can enter the structure of C2S and possibly form solid solutions and different phosphatic calcium silicate phases in C2S–C3P system. Depending on the P2O5 concentration in mixtures, three distinct phases are formed: larnite (2CaO•SiO2), Ca14,92(PO4)2,35(SiO4)5,65 and 5CaO•SiO2•P2O5, as detected by XRD. Local microanalysis de-monstrated the presence of calcium phosphate epicenters (C3P) containing SiO2, calcium sili-cate (C2S) zones with minimum content of P2O5 and intermediary areas of various phosphatic calcium silicates. The formation of two distinct islets of C2S and C3P is due the affinity of acid oxides (SiO2, P2O5) towards the basic one (CaO) during the sol-gel process. Then, the formation of various phosphatic calcium silicates results from the diffusion of P2O5 and SiO2 towards calcium silicate and calcium phosphate, respectively.