Evolution of microstructure and performance in magnesium potassium phosphate ceramics: Role of sintering temperature of MgO powder

被引:45
作者
Viani, Alberto [1 ]
Sotiriadis, Konstantinos [1 ]
Sasek, Petr [1 ]
Appavou, Marie-Sousai [2 ]
机构
[1] Ctr Excellence Telc, Inst Theoret & Appl Mech AS CR, Batelovska 485, CZ-58856 Telc, Czech Republic
[2] Forschungszentrum Julich, Julich Ctr Neutron Sci JCNS, Aussenstelle MLZ, Lichtenbergstr 1, D-85747 Garching, Germany
关键词
Chemically-bonded ceramics; X-ray diffraction (XRD); Small angle neutron scattering (SANS); Microstructure; Amorphous materials; QUANTITATIVE PHASE-ANALYSIS; THERMAL TRANSFORMATION; FINE POROSITY; FLY-ASH; X-RAY; CEMENT; SCATTERING; KINETICS; STRUVITE; PRODUCT;
D O I
10.1016/j.ceramint.2016.07.182
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The reactivity of the MgO powder employed in the formulation of Mg-K phosphate ceramics can be modulated through the calcination temperature of MgCO3 source material, which has a direct impact on production costs. Upon annealing, MgO undergoes sintering, and in order to optimize the design of products for applications, it is of primary importance to disclose the link between the sintering temperature, reaction mechanisms, microstructure and performance in this class of ceramics. Small angle neutron scattering was used to measure the specific surface area of pores in samples aged 30 days produced with 5 different MgO powders, and to follow the evolution of pore size distribution during the setting reaction, in a time-resolved experiment. Quantification of amorphous and crystalline fraction up to 28 days was accomplished in synchronous with flexural strength tests. Results indicate that mechanical properties improve thanks to the progressive buildup of a pervasive network of tabular crystals filling the entire volume. Increasing the sintering temperature above 1500 degrees C yields a more compact ceramic, with less, but larger, pores, containing more crystalline fraction and less amorphous. This is consistent with the recently proposed mechanisms describing the ceramic setting reaction. The analysis of the fractured surface suggests that strength might be effectively improved modifying the density and orientation of crystals in the ceramic volume, a way for engineering new tailor-made ceramics. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:16310 / 16316
页数:7
相关论文
共 47 条
  • [1] Study of temperature effect on microstructures of MCIC ceramic substrate using small angle neutron scattering
    Ahmad, M. H. Al Rashid Megat
    Ibrahim, A.
    Mohamed, A. A.
    Alias, R.
    Alias, N. H.
    Mahmood, C. S.
    Putra, E. G. Rachman
    Ikram, A.
    Mat, A. F. Awang
    [J]. ADVANCES IN APPLIED CERAMICS, 2009, 108 (04) : 199 - 202
  • [2] Characterization of ceramics by X-ray and neutron small-angle scattering
    Allen, AJ
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2005, 88 (06) : 1367 - 1381
  • [3] Small-angle neutron scattering studies of ceramic nanophase materials
    Allen, AJ
    Krueger, S
    Long, GG
    Kerch, HM
    Hahn, H
    Skandan, G
    [J]. NANOSTRUCTURED MATERIALS, 1996, 7 (1-2): : 113 - 126
  • [4] DEVELOPMENT OF THE FINE POROSITY AND GEL STRUCTURE OF HYDRATING CEMENT SYSTEMS
    ALLEN, AJ
    OBERTHUR, RC
    PEARSON, D
    SCHOFIELD, P
    WILDING, CR
    [J]. PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES, 1987, 56 (03): : 263 - 288
  • [5] [Anonymous], 1982, Small angle x-ray scattering, DOI DOI 10.1002/ACTP.1985.010360520
  • [6] [Anonymous], 1983, FRACTURE MECH CERAMI
  • [7] Balzar D, 1999, MICROSTRUCT ANAL DIF, P44
  • [8] An Overview of The Effects of Thermal Processing on Bioactive Glasses
    Bellucci, D.
    Cannillo, V.
    Sola, A.
    [J]. SCIENCE OF SINTERING, 2010, 42 (03) : 307 - 320
  • [9] QUANTITATIVE PHASE-ANALYSIS USING THE RIETVELD METHOD
    BISH, DL
    HOWARD, SA
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1988, 21 (02) : 86 - 91
  • [10] Brantley SL, 2008, Kinetics of Water-Rock Interaction, DOI DOI 10.1007/978-0-387-73563-4