期刊
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
卷 91, 期 9, 页码 3052-3057出版社
WILEY
DOI: 10.1111/j.1551-2916.2008.02577.x
关键词
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资金
- Grant Agency of the Czech Republic [203/05/2309]
- Ministry of Industry and Trade of the Czech Republic [FI-IM/079, FI-TA4/ 068]
Ion exchange of Na+ ions in a geopolymer by Cs+, NH4+, and Co2+ was used to characterize the accessibility of the inner volume of a Na-geopolymer (Si/Al 1.8) and the size of the rings controlling the mobility of cations in the geopolymer matrix. Ultraviolet (UV)-visible (vis) spectroscopy of Co2+ ions in the Co2+-exchanged geopolymer was used to characterize the local geometry of the Co2+ ions and the regularity and shape of local structures accommodating these Co2+ ions in the geopolymer matrix. Na-geopolymers exhibit ion-exchange properties similar to those of zeolites. All Na+ ions balancing Al atoms of the network of the as-prepared geopolymer could be replaced (ion-exchanged) by NH4+ or Co2+ ions. By analogy to zeolites, this indicates that all the Al atoms are accessible through rings containing at least eight Al and Si atoms. Co2+ ions in the geopolymer network are accommodated in two regular types of deformed six-membered or eight-membered rings. As indicated by the lower extent of Cs+ exchange, only one-half of the Al atoms are simultaneously accessible through 10-membered or larger rings. This indicates that neither regular alumosilicate six-membered rings nor the hexagonal prisms typical of some zeolitic structures are present in the geopolymer network.
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