Mechanism of Phosphorus Enrichment in Dephosphorization Slag Produced Using the Technology of Integrating Dephosphorization and Decarburization

In order to better understand and develop the technology of integrating dephosphorization and decarburization in a single converter (abbreviated as IDDSC), the relevant thermodynamic issues were discussed by calculation. Based on the thermodynamic calculation, the bridges between the phosphorus distribution ratio, temperature, and slag composition were constructed. Besides, the connections between the dephosphorization behavior and the microstructure of slag were also established by investigating four heats of hot metal smelt using IDDSC technology. As a result, the mechanism of phosphorus enrichment in the dephosphorization slag was revealed. Also, the results show that the dephosphorization efficiency increases gradually with increasing slag basicity. While the dephosphorization efficiency increases first and then decreases with the increase of FeO content in slag. There is a competition relationship between P2O5 and FeO in reacting with CaO and SiO2. When CaO/FeO is relatively high, not enough FeO is provided. Thus P2O5 is in priority to react with CaO and SiO2 through [3n + 2](CaO) + 2SiO2 + n(P2O5) = n(3CaO·P2O5)-2CaO·SiO2(s), generating P2O5-rich nC2S-C3P solid solution which promotes the removal of [P] from the hot metal. When CaO/FeO is relatively low, FeO competes over P2O5 in reacting with CaO and SiO2 through a(CaO) + b(SiO2) + c(FeO) = aCaO·bSiO2·cFeO(s), generating CaFeSiO4 instead of P2O5-rich solid solution. As a consequence, the slag with low CaO/FeO shows a poor dephosphorization ability

Decorated CuO nanoparticles over chitosan-functionalized magnetic nanoparticles: Investigation of its anti-colon carcinoma and anti-gastric cancer effects

In this study, a green protocol for supporting CuO nanoparticles over chitosan-modified amino-magnetic nanoparticles is described. The physicochemical and morphological properties of the desired nanocomposite assessed by various techniques like ICP, FT-IR, FE-SEM, EDX, TEM, XRD and VSM. In the oncological part of the recent study, the Cu(NO3)2, Fe3O4, and Fe3O4-NH2@CS/CuO nanocomposite cell viability was very low against human gastric cancer cell lines i.e. MKN45, AGS, and KATO III and human colorectal carcinoma cell lines i.e. HT-29, HCT 116, HCT-8 [HRT-18], and Ramos.2G6.4C10. The IC50 of Fe3O4-NH2@CS/CuO nanocomposite against MKN45, AGS, KATO III, HT-29, HCT 116, HCT-8 [HRT-18], and Ramos.2G6.4C10 cell lines were 517, 525, 544, 282, 214, 420, and 477 µg/mL, respectively. Thereby, the best anti-gastro-duodenal cancers findings of our Fe3O4-NH2@CS/CuO nanocomposite was seen in the HCT 116 cell line case

Mechanism of Phosphorus Enrichment in Dephosphorization Slag Produced Using the Technology of Integrating Dephosphorization and Decarburization

In order to better understand and develop the technology of integrating dephosphorization and decarburization in a single converter (abbreviated as IDDSC), the relevant thermodynamic issues were discussed by calculation. Based on the thermodynamic calculation, the bridges between the phosphorus distribution ratio, temperature, and slag composition were constructed. Besides, the connections between the dephosphorization behavior and the microstructure of slag were also established by investigating four heats of hot metal smelt using IDDSC technology. As a result, the mechanism of phosphorus enrichment in the dephosphorization slag was revealed. Also, the results show that the dephosphorization efficiency increases gradually with increasing slag basicity. While the dephosphorization efficiency increases first and then decreases with the increase of FeO content in slag. There is a competition relationship between P2O5 and FeO in reacting with CaO and SiO2. When CaO/FeO is relatively high, not enough FeO is provided. Thus P2O5 is in priority to react with CaO and SiO2 through [3n + 2](CaO) + 2SiO2 + n(P2O5) = n(3CaO·P2O5)-2CaO·SiO2(s), generating P2O5-rich nC2S-C3P solid solution which promotes the removal of [P] from the hot metal. When CaO/FeO is relatively low, FeO competes over P2O5 in reacting with CaO and SiO2 through a(CaO) + b(SiO2) + c(FeO) = aCaO·bSiO2·cFeO(s), generating CaFeSiO4 instead of P2O5-rich solid solution. As a consequence, the slag with low CaO/FeO shows a poor dephosphorization ability

The improvement of phase-change properties on Ge

Ge2Sb2Te5 (GST)/Ge superlattice-like (SLL) films are investigated in the study. Reflection spectra measurements with polarized excitations and atomic force microscopy are carried out to investigate phase-change properties. Because of the Ge cladding films, GST phase-change properties could be improved. The thicker Ge cladding film is believed could lead to a relatively larger grain size. GST phase-change behaviors in the films can be adjusted by changing the layer thickness. We found the [GST(5 nm)/Ge(5 nm)]10 SLL film has the higher crystallization temperature, faster phase change speed, better thermal stability and relatively smooth surface. The GST/Ge SLL films may have the potential for commercial use

Solvothermal Metal Metathesis on a Metal–Organic Framework with Constricted Pores and the Study of Gas Separation

Metal–organic frameworks (MOFs) with constricted pores can increase the adsorbate density of gas and facilitate effective CO₂ separation from flue gas or natural gas due to their enhanced overlapping of potential fields of the pores. Herein, an MOF with constricted pores, which was formed by narrow channels and blocks of functional groups, was fabricated from the assembly of a methyl-functionalized ligand and Zn­(II) centers (termed NPC-7-Zn). Structural analysis of the as-synthesized NPC-7-Zn reveals a series of zigzag pores with pore diameters of ∼0.7 nm, which could be favorable for CO₂ traps. For reinforcing the framework stability, a solvothermal metal metathesis on the pristine MOF NPC-7-Zn was performed, and a new Cu­(II) MOF (termed NPC-7-Cu) with an identical framework was produced. The influence of the reaction temperatures on the metal metathesis process was investigated. The results show that the constricted pores in NPC-7-Zn can induce kinetic issues that largely slow the metal metathesis process at room temperature. However, this kinetic issue can be solved by applying higher reaction temperatures. The modified MOF NPC-7-Cu exhibits significant improvements in framework stability and thus leads to a permanent porosity for this framework. The constricted pore structure enables enhanced potential fields for these pores, rendering this MOF with high adsorbate densities for CO₂ and high adsorption selectivity for a CO₂/N₂ gas mixture. The adsorption kinetic studies reveal that CH₄ has a faster diffusion rate constant than CO₂, showing a surface diffusion controlled mechanism for CO₂ and CH₄ adsorption