Immobilization of Cu(II) and Zn(II) into hydrocalumite - An X-ray absorption fine structure (XAFS) investigation

被引:2
作者
Wang, Qiaorui [1 ,2 ,3 ]
Xi, Shibo [4 ]
Zheng, Chunli [3 ]
Geng, Guoqing [1 ]
机构
[1] Natl Univ Singapore, Dept Civil & Environm Engn, Singapore 117576, Singapore
[2] Yanan Univ, Sch Petr Engn & Environm Engn, Yanan Key Lab Agr Solidiste Resource Utilizat, Yanan 716000, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Environm Sci & Engn, Xian 710049, Peoples R China
[4] ASTAR, Inst Chem & Engn Sci, 1 Pesek Rd, Singapore 627833, Singapore
关键词
Hydrocalumite; Cu; Zn; Immobilization; EXAFS spectroscopy; ENVIRONMENTALLY SIGNIFICANT METALS; CHEMICAL SPECIATION; SORPTION MECHANISMS; ZINC; ETTRINGITE; HYDRATION; REMOVAL;
D O I
10.1016/j.conbuildmat.2024.136828
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The fate of heavy metals is crucial to the reuse of municipal waste incineration ash (MWIA) as construction materials. It is, however, not completely clear how they interact with cementitious phases at the molecular scale. This study investigated the uptake and speciation of Cu(II) and Zn(II) during the generation of Al-hydrocalumitetype high-pH phases through co-precipitation and adsorption experiments. Hydrocalumite (Hc) and minor phases, such as calcite and hydrogarnet, were identified as primary phases using X-ray diffraction (XRD). The characterization of Hc+Cu(II), Hc+Zn(II), and Hc+Cu(II)+Zn(II) via XRD, SEM, and bulk Cu(II)/Zn(II) EXAFS showed that both Cu(II) and Zn(II) exists as the surface/interlayer adsorption on the Hc+Cu(II)/Hc+Zn(II) and Hc+Cu(II)+Zn(II). Thermodynamic calculations support the experimental observations for the bulk phase. This study help understand the interacting mechanism between Cu(II)/Zn(II) and Hc phase, and pave the way of safe utilization of heavy-metal-containing waste as supplementary cementitious materials.
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页数:9
相关论文
共 41 条
[21]   The principles determining the structure of complex ionic crystals [J].
Pauling, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1929, 51 (1-4) :1010-1026
[22]   Immobilization of heavy metals, selenate, and sulfate from a hazardous industrial side stream by using calcium sulfoaluminate-belite cement [J].
Piekkari, Katri ;
Ohenoja, Katja ;
Isteri, Visa ;
Tanskanen, Pekka ;
Illikainen, Mirja .
JOURNAL OF CLEANER PRODUCTION, 2020, 258
[23]   Chemical speciation of environmentally significant metals with inorganic ligands -: Part 2:: The Cu2+-OH-, Cl-, CO32-, SO42-, and PO43- systems -: (IUPAC technical report) [J].
Powell, Kipton J. ;
Brown, Paul L. ;
Byrne, Robert H. ;
Gajda, Tamas ;
Hefter, Glenn ;
Sjoeberg, Staffan ;
Wanner, Hans .
PURE AND APPLIED CHEMISTRY, 2007, 79 (05) :895-950
[24]   Chemical speciation of environmentally significant metals with inorganic ligands. Part 5: The Zn2+ + OH-, Cl-, CO32-, SO42-, and PO43-systems (IUPAC Technical Report) [J].
Powell, Kipton J. ;
Brown, Paul L. ;
Byrne, Robert H. ;
Gajda, Tamas ;
Hefter, Glenn ;
Leuz, Ann-Kathrin ;
Sjoberg, Staffan ;
Wanner, Hans .
PURE AND APPLIED CHEMISTRY, 2013, 85 (12) :2249-2311
[25]  
SACERDOTI M, 1988, NEUES JB MINER MONAT, P462
[26]   Immobilizing Pertechnetate in Ettringite via Sulfate Substitution [J].
Saslow, Sarah A. ;
Kerisit, Sebastien N. ;
Varga, Tamas ;
Mergelsberg, Sebastian T. ;
Corkhill, Claire L. ;
Snyder, Michelle M., V ;
Avalos, Nancy M. ;
Yorkshire, Antonia S. ;
Bailey, Daniel J. ;
Crum, Jarrod ;
Asmussen, R. Matthew .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2020, 54 (21) :13610-13618
[27]   Kinetic controls on Cu and Pb sorption by ferrihydrite [J].
Scheinost, AC ;
Abend, S ;
Pandya, KI ;
Sparks, DL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (06) :1090-1096
[28]  
Seetawan U., 2011, Materials Sciences and Applications, V2, P1302, DOI [DOI 10.4236/MSA.2011.29176, DOI 10.4236/MSA]
[29]   Immobilization of Hg(II) by Coprecipitation in Sulfate-Cement Systems [J].
Serrano, Susana ;
Vlassopoulos, Dimitri ;
Bessinger, Brad ;
O'Day, Peggy A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2012, 46 (12) :6767-6775
[30]  
Splittgerber F, 2003, P 11 INT C CHEM CEM, P1282, DOI [10.13140/2.1.2201.3766, DOI 10.13140/2.1.2201.3766]