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Strength Development and Products Evolution of β-C2S and γ-C2S Induced by Accelerated Carbonation Curing 被引量:5

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摘要 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.
作者 FANG Yanfeng LIU Zhichao WANG Qinghe ZHANG Yuzhuo ZHANG Miao 王晴 FANG Yanfeng;LIU Zhichao;WANG Qinghe;ZHANG Yuzhuo;ZHANG Miao;WANG Qing(School of Materials Science and Engineering,Shenyang Jianzhu University,Shenyang 110168,China;School of Materials Science and Engineering,Wuhan University of Technology,Wuhan 430070,China;School of Civil Engineering,Shenyang Jianzhu University,Shenyang 110168,China)
出处 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2020年第6期1053-1060,共8页 武汉理工大学学报(材料科学英文版)
基金 Funded by the National Natural Science Foundation of China(Nos.51808354,51808351 and 51808532) the National Natural Science Foundation of Liaoning,China(No.20180550127) the China Postdoctoral Science Foundation(No.2018M641712) the State Key Laboratory of Silicate Materials for Architectures(Wuhan University of Technology)。
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  • 1G1BBINS J, CHALMERS H. Carbon capture and storage [J]. Energy Policy, 2008, 36(12): 4317-4322.
  • 2SEIFRITZ W. CO2 disposal by means of silicates [J]. Nature, 1990, 345: 486.
  • 3HUIJGEN W J, WITKAMP G, COMANS R N. Mineral CO2 sequestration by steel slag carbonation [J]. Environ Sei Technol, 2005, 39(24): 9676-9682.
  • 4BOBICKI E R, L1U Q, XU Z, et al. Carbon capture and storage using alkaline industrial wastes [J]. Prog Energ Combust, 2012, 38(2): 302-320.
  • 5HUHGEN W J, COMANS R N. Carbonation of steel slag for CO2 sequestration: leaching of products and reaction mechanisms [J]. Environ Set Technol, 2006, 40(8): 2790-2796.
  • 6TERAMURA S, ISU N, INAGAKI K. New building material from waste concrete by carbonation [J]. J Mater Civil Eng, 2000, 12(4): 288-293.
  • 7DIAMOND S. Cement paste microstructure--an overview at several levels: Proc. Conf. hydraulic cement pastes: their structure and properties [C], 1976.
  • 8BLACKL, BREEN C, YARWOOD J, et al. Structural features of C-S-H (I) and its carbonation in air---a Raman spectroscopic study. Part II: carbonated phases [J]. J Am Ceram Soc, 2007, 90(3): 908-917.
  • 9MORALES-FLOREZ V, DE LA ROSA-FOX N. Structure of supercritically dried calcium silicate hydrates (C-S-H) and structural changes induced by weathering [J]. J Mater Sei, 2013, 48(14): 5022-5028.
  • 10BLACK L, GARBEVK G I. Surface carbonation of synthetic C-S-H samples: A comparison between fresh and aged C-S-H using X-ray photoelectron spectroscopy[J]. Cem Concr Res, 2008, 38(6): 745-750.

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