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Carbonation of Dicalcium Silicate Enhanced by Ammonia Bicarbonate and Its Mechanism
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作者 周浩 刘鹏 +1 位作者 WANG Fazhou HU Chuanlin 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS CSCD 2024年第1期69-74,共6页
The strength development law of γ-type dicalcium silicate (γ-C_(2)S) under different carbonation processes was investigated,and the carbonation mechanism of γ-C_(2)S under the action of NH_(4)HCO_(3) was clarified ... The strength development law of γ-type dicalcium silicate (γ-C_(2)S) under different carbonation processes was investigated,and the carbonation mechanism of γ-C_(2)S under the action of NH_(4)HCO_(3) was clarified by using a wide range of test methods,including XRD and SEM.A method of saturated NH_(4)HCO_(3) solution as a curing agent was identified to improve the carbonation efficiency and enhance the carbonation degree of γ-C_(2)S,and then a high-strength carbonated specimen was obtained.Microhardness analysis and SEM morphology analysis were conducted on the carbonised specimens obtained under atmospheric pressure carbonisation conditions using the curing agent.It was found that γ-C_(2)S could perform carbonisation well under atmospheric pressure,which promoted the carbonisation efficiency and decreased the carbonisation cost simultaneously.Therefore,a new carbonisation process solution was proposed for the rapid carbonisation of γ-C_(2)S. 展开更多
关键词 type dicalcium silicate carbonization process curing agent atmospheric carbonization
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Adsorption of sodium polyacrylate at interface of dicalcium silicate-sodium aluminate solution 被引量:5
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作者 于海燕 潘晓林 +3 位作者 丁婷婷 张武 刘涵 毕诗文 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2011年第10期2323-2326,共4页
The adsorption isotherm of sodium polyacrylate on dicalcium silicate(2CaO-SiO2) in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the... The adsorption isotherm of sodium polyacrylate on dicalcium silicate(2CaO-SiO2) in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the adsorption behavior belongs to L-type,according with the monolayer adsorption model of Langmuir equation.The surface coverage of sodium polyacrylate is 1.06 mol/μm2.The relation curve between the surface pressure and the molecular area of adsorption film was obtained by Gibbs formula.The variation of interfacial energy caused by adsorption as well as the relationship between the relation curve and the type of adsorption was discussed. 展开更多
关键词 sodium aluminate solution sodium polyacrylate dicalcium silicate INTERFACE ADSORPTION
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Effect of Na_(2)O on transition and stability of dicalcium silicate based on sintering process 被引量:2
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作者 PAN Xiao-lin LYU Zhong-yang +1 位作者 ZHANG Can YU Hai-yan 《Journal of Central South University》 SCIE EI CAS CSCD 2022年第4期1161-1172,共12页
The phase transition,morphology,stability and pulverization performance of dicalcium silicate(C_(2)S)with different Na_(2)O additions during the high-temperature sintering process were studied using XRD,SEM-EDS,FT-IR,... The phase transition,morphology,stability and pulverization performance of dicalcium silicate(C_(2)S)with different Na_(2)O additions during the high-temperature sintering process were studied using XRD,SEM-EDS,FT-IR,and Raman spectra methods.When the CaO to SiO_(2) molar ratio is 2.0 and the Na_(2)O to SiO_(2) molar ratio is below 0.20,the crystalline calcium silicate compounds includeγ-C_(2)S andβ-C_(2)S.As the Na_(2)O addition increases,the proportion,crystallinity and grain size ofβ-C_(2)S in the sintered products increase,those parameters ofγ-C_(2)S decrease,and the content of amorphous phase increases.Na_(2)O mainly forms solid solutions inβ-C_(2)S and inhibits the transition ofβ-C_(2)S toγ-C_(2)S,resulting in the sintered products unpulverized.The stability of sintered products in alkali solution decreases significantly with the increasing Na_(2)O additions,and theβ-C_(2)S solid solution with Na_(2)O is less stable thanγ-C_(2)S.The mechanism that Na_(2)O affects the transition of C_(2)S as well as its stability was also discussed,which can give actual guidance for the treatment of low-grade alumina-containing resources by the sintering process. 展开更多
关键词 dicalcium silicate Na_(2)O crystal structure STABILITY SINTERING
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Formation of apatite on the surface of plasmas prayed dicalcium silicate coating
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《Chinese Journal of Biomedical Engineering(English Edition)》 2001年第3期124-126,共3页
关键词 SBF Formation of apatite on the surface of plasmas prayed dicalcium silicate coating
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Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs 被引量:3
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作者 Qianting Luo Xingyang Li +9 位作者 Wenchao Zhong Wei Cao Mingjing Zhu Antong Wu Wanyi Chen Zhitong Ye Qiao Han Duraipandy Natarajan Janak L.Pathak Qingbin Zhang 《Regenerative Biomaterials》 SCIE EI 2022年第1期93-106,共14页
Dicalcium silicate(Ca_(2)SiO_(4),C_(2)S)has osteogenic potential but induces macrophagic inflammation.Mitochondrial function plays a vital role in macrophage polarization and macrophagic inflammation.The mitochondrial... Dicalcium silicate(Ca_(2)SiO_(4),C_(2)S)has osteogenic potential but induces macrophagic inflammation.Mitochondrial function plays a vital role in macrophage polarization and macrophagic inflammation.The mitochondrial function of C_(2)S-treated macrophages is still unclear.This study hypothesized:(i)the C_(2)S modulates mitochondrial function and autophagy in macrophages to regulate macro-phagic inflammation,and(ii)C_(2)S-induced macrophagic inflammation regulates osteogenesis.We used RAW264.7 cells as a model of macrophage.The C_(2)S(75–150μg/ml)extract was used to analyze the macrophagic mitochondrial function and macrophagemediated effect on osteogenic differentiation of mouse bone marrow-derived mesenchymal stem cells(BMSCs).The results showed that C_(2)S extract(150μg/ml)induced TNF-α,IL-1βand IL-6 production in macrophages.C_(2)S extract(150μg/ml)enhanced reactive oxygen species level and intracellular calcium level but reduced mitochondrial membrane potential and ATP production.TEM images showed reduced mitochondrial abundance and altered the mitochondrial morphology in C_(2)S(150μg/ml)-treated macrophages.Protein level expression of PINK1,Parkin,Beclin1 and LC3 was upregulated but TOMM20 was downregulated.mRNA sequencing and KEGG analysis showed that C_(2)S-induced differentially expressed mRNAs in macrophages were mainly distributed in the essential signaling pathways involved in mitochondrial function and autophagy.The conditioned medium from C_(2)S-treated macrophage robustly promoted osteogenic differentiation in BMSCs.In conclusion,our results indicate mitochondrial dysfunction and autophagy as the possible mechanism of C_(2)S-induced macrophagic inflammation.The promotion of osteogenic differentiation of BMSCs by the C_(2)S-induced macrophagic inflammation suggests the potential application of C_(2)S in developing immunomodulatory bone grafts. 展开更多
关键词 dicalcium silicate macrophagic inflammation mitochondrial function AUTOPHAGY OSTEOGENESIS
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Mechanism of direct CO_(2) sequestration by alkali metal K-activated steel slag
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作者 Rong Sun Xu-chao Wang +3 位作者 Wei-cheng Xu Ru-fei Wei Jie Lei Hong-ming Long 《Journal of Iron and Steel Research International》 2025年第6期1540-1554,共15页
CO_(2)sequestration through steel slag is one of the effective approaches to simultaneously realize the resource utilization of industrial solid waste,reduce carbon emissions,and enhance the stability of steel slag as... CO_(2)sequestration through steel slag is one of the effective approaches to simultaneously realize the resource utilization of industrial solid waste,reduce carbon emissions,and enhance the stability of steel slag as a construction base,with considerable application prospects.Nevertheless,the components responsible for CO_(2)sequestration in steel slag predominantly exist as silicates,whose chemical inertness leads to suboptimal CO_(2)sequestration efficiency in the slag.Based on the strategy of activating the silicate components in steel slag with the alkali metal potassium(K)to improve the CO_(2)sequestration performance of steel slag,both experiments and theoretical calculations were performed to give a deep insight into the effect and mechanism of K modification on enhancing the CO_(2)sequestration capability of steel slag.In experiments,CO_(2)sequestration capacity of steel slag modified with 3 wt.%K reached 100.15 g/kg at 1000 K.Theoretical analysis has revealed that although K exhibits low reactivity,it enhances the electronic transition and amplifies charge localization at specific sites within Ca_(2)SiO_(4),consequently improving its CO_(2)sequestration capacity.However,an excessive doping of K led to the partial inactivation of some active sites within Ca_(2)SiO_(4).Furthermore,CO_(2)chemisorption on Ca_(2)SiO_(4)surface predominantly occurs through the chelate configuration of CO_(3)^(2−),suggesting the formation of a CaCO_(3)precursor.Thus,both the experimental results and theoretical calculations reveal the role of K on enhancing CO_(2)sequestration capability of steel slag.In summary,K modification offers promising prospects for improving CO_(2)sequestration properties of steel slag and provides support for the industrial implementation of carbon sequestration by steel slag. 展开更多
关键词 K-modified steel slag CO_(2)sequestration dicalcium silicate Density functional theory
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Calcium Silicate Cements Application in Lateral Root Perforation Repair: A Case Report with 16-Month Follow-Up
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作者 Juan G. Robledo Pablo A. Rodríguez 《Open Journal of Stomatology》 2021年第8期317-324,共8页
Lateral root perforations are unfortunate procedures during endodontic treatment and often lead to tooth extraction. Conditioning factors such as time, size, location, inappropriate disinfection and sealing, are indis... Lateral root perforations are unfortunate procedures during endodontic treatment and often lead to tooth extraction. Conditioning factors such as time, size, location, inappropriate disinfection and sealing, are indispensable to achieve acceptable long-term outcomes. Calcium silicate cements are bioactive materials used for perforation repair. They can be set in moist environments such as blood, saliva and dentinal fluid making them a reliable material for clinical applications. This case report describes the treatment and repair after a 16-month follow-up of a lateral root perforation of the maxillary lateral incisor. 展开更多
关键词 ENDODONTICS Lateral Root Perforation Tri/dicalcium silicate Cements Mineral Trioxide Aggregate Bioactive Materials
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Effect of P addition on mineral transition of CaO-Al_2O_3-SiO_2 system during high-temperature sintering 被引量:7
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作者 Hai-yan YU Xiao-lin PAN +1 位作者 Kai-wei DONG Yan WU 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2019年第3期650-656,共7页
The mineral transition, microstructure and self-pulverization as well as the Al2O3 leaching performance of calcium aluminate clinkers with different P additions in CaO-Al2O3-SiO2 system during high-temperature sinteri... The mineral transition, microstructure and self-pulverization as well as the Al2O3 leaching performance of calcium aluminate clinkers with different P additions in CaO-Al2O3-SiO2 system during high-temperature sintering were systematically studied by XRF, XRD, SEM-EDS and DSC-TG technologies. The clinkers sintered at 1350 °C mainly contain 12CaO·7Al2O3, CaO·Al2O3,β-2CaO·SiO2 and γ-2CaO·SiO2. The content of β-2CaO·SiO2 increases while the content of γ-2CaO·SiO2 decreases as the P addition increases. The self-pulverization property of clinkers deteriorates with increasing P addition. P distributes evenly in the clinkers, and inhibits the transformation of β-2CaO·SiO2 to γ-2CaO·SiO2. The cell volumes of 12CaO·7Al2O3 and CaO·Al2O3 decrease and increase respectively as the P addition increases, and P decreases their formation temperatures. The Al2O3 leaching rate of calcium aluminate clinkers decreases obviously with increasing P addition, which decreases form 95.01% to 83.84% as the P addition increases from 0 to 0.85%. 展开更多
关键词 lime-sinter process calcium aluminate dicalcium silicate crystal structure self-pulverization performance LEACHING
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Strength Development and Products Evolution of β-C2S and γ-C2S Induced by Accelerated Carbonation Curing 被引量:7
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作者 FANG Yanfeng LIU Zhichao +3 位作者 WANG Qinghe ZHANG Yuzhuo ZHANG Miao WANG Qing 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2020年第6期1053-1060,共8页
Low calcium β-C2S and γ-C2S minerals with low hydration activity was activated by accelerated carbonation curing to be used as new binding materials.Synthetic β-C2S and γ-C2S were synthetized and compacted to prep... Low calcium β-C2S and γ-C2S minerals with low hydration activity was activated by accelerated carbonation curing to be used as new binding materials.Synthetic β-C2S and γ-C2S were synthetized and compacted to prepare cube samples and then subjected to CO2 chamber for accelerated carbonation curing.The CO2 uptake,mechanical strength,and microstructure changes of β-C2S and γ-C2S were analyzed by TG,XRD,MAS-NMR,and MIP.The experimental results indicate the CO2 uptake of γ-C2S is much higher than that of β-C2S,but the compressive strength of γ-C2S samples is lower than that of β-C2S.Calcium carbonate and other carbonation products stack in the pore structure and the porosity is reduced from about 42% to 30.1% and 22.0% for β-C2S and γ-C2S samples after 2 h carbonation curing,respectively.The difference in compressive strength development is caused by the different properties of carbonation products.Except for calcium carbonate,there also exists obvious difference in properties of amorphous phases:γ-C2S formed silica gel in the whole carbonation progress;however,β-C2S can react to produce silica gel and C-S-H gel with high Van der Waals forces,and C-S-H gel will continue to react with CO2 to form calcium carbonate and silica gel in later carbonation reaction;In addition the microhardness of carbonated β-C2S was more higher than that of γ-C2S. 展开更多
关键词 dicalcium silicate CARBONATION CO2 uptake HARDENING microstructure
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A COMMENT ON THE SOLID SOLUTION OF C_2S AND ITS MATCHING PHASE
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作者 陶景飏 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 1989年第2期25-40,共16页
On the bases of practical investigation, the paper, through synthesizing lots of documents and materials, discusses the stability and crystalline pattern transforming of C_2S, the hydrating and hardening mechanism of ... On the bases of practical investigation, the paper, through synthesizing lots of documents and materials, discusses the stability and crystalline pattern transforming of C_2S, the hydrating and hardening mechanism of its solid solution as well as the affect of adding ions. In recent years, the research on C_2S has been attached importance to and has achieved obvious success, especially in the study of the match phase of C_2S solid solution, many cement systems with fine characteristics have been formed. It shows it's quite easy for C_2S to match other minerals, which plays an important role in saving energy, improving cement properties and developing new cement materials. The broad propspects are revealed in C_2S studying area. 展开更多
关键词 dicalcium silicate CEMENT Solid solution.
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The Microstructure and Chemical Bonds of β-C_2S Under the High Energy Ball Grinding Function
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作者 胡曙光 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2006年第1期150-153,共4页
Using the laser granularity survey technology , logy, X-ray powder diffraction, scanning electron microscopy (SEM) and infrared spectrum anal)sis methods, we studied the microscopic structure and chemical bonds cha... Using the laser granularity survey technology , logy, X-ray powder diffraction, scanning electron microscopy (SEM) and infrared spectrum anal)sis methods, we studied the microscopic structure and chemical bonds changes of β-C2 S monomineral under the high energy ball grinding function. The result indicates that, continuously under the mechanical power, β-C2 S crystal size would decrease, the micro strain and the effective Beff parameter would increase, and the amorphous phases would be presented. Furthermore, the mechanical power would cause Si-O bond broken and reorganized, the specific surface area would increase, the energy of micro-powder agglomeration vibration would be enhanced and the crystal would be disordered. Finally, β- C2 S was caused to have the mechanochemical change and the activity enhancement. 展开更多
关键词 dicalcium silicate crystal microscopic structure MECHANOCHEMISTRY
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Design and experiment on concentration of phosphorus in factory converter slags
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作者 WU Xingrong AN Jinan +1 位作者 LI Liaosha CHEN Ronghuan 《Baosteel Technical Research》 CAS 2010年第S1期140-,共1页
The phosphorus-concentrating phase in the converter slags was designed and simulated by synthetic converter slag.The distribution of phosphorus in factory converter slags was also analyzed by scanning electron microsc... The phosphorus-concentrating phase in the converter slags was designed and simulated by synthetic converter slag.The distribution of phosphorus in factory converter slags was also analyzed by scanning electron microscope(SEM) and X-ray diffraction(XRD).Then factory converter slags were modified by addition of SiO_2 and heated to 1540℃and then cooled to room temperature.The results showed that the phosphorus in the factory converter slags was mostly distributed in two phases:dicalcium silicate (C_2S) and tricalcium silicate(C_3S) by formation of solid solution,and with a little in matrix.Whereas,in the synthetic slags with the basicity close to 3,phosphorus was almost concentrated in phase of C_2S(Pconcentrating phase) in which the contents of P_2O_5 reach to 7.74%.This lays a good foundation for grinding and separation of P- concentrating phase. 展开更多
关键词 PHOSPHORUS converter slags p-concentrating phase dicalcium silicate
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