Summary
Zeolites are microporous, crystalline aluminosilicate materials commonly used as commercial adsorbents and catalysts. They mainly consist of silicon, aluminium, oxygen, and have the general formula M1/nn+(AlO2)-(SiO2)x・yH2O where M1/nn+ is either a metal ion or H+. These positive ions can be exchanged for others in a contacting electrolyte solution. H+ exchanged zeolites are particularly useful as solid acid catalysts. The term zeolite was originally coined in 1756 by Swedish mineralogist Axel Fredrik Cronstedt, who observed that rapidly heating a material, believed to have been stilbite, produced large amounts of steam from water that had been adsorbed by the material. Based on this, he called the material zeolite, from the Greek ζέω (zéō), meaning "to boil" and λίθος (líthos), meaning "stone". Zeolites occur naturally but are also produced industrially on a large scale. , 253 unique zeolite frameworks have been identified, and over 40 naturally occurring zeolite frameworks are known. Every new zeolite structure that is obtained is examined by the International Zeolite Association Structure Commission (IZA-SC) and receives a three letter designation. Zeolites are white solids with ordinary handling properties, like many routine aluminosilicate minerals, e.g. feldspar. They have the general formula where M+ is usually H+ and Na+. The Si/Al ratio is variable, which provides a means to tune the properties. Zeolites with a Si/Al ratios higher about 3 are classified as high-silica zeolites, which tend to be more hydrophobic. The H+ and Na+ can be replaced by diverse cations, because zeolites have ion exchange properties. The nature of the cations influences the porosity of zeolites. Zeolites have microporous structures with a typical diameter of 0.3–0.8 nm. Like most aluminosilicates, the framework is formed by linking of aluminum and silicon atoms by oxides. This linking leads to a 3-dimensional network of Si-O-Al, Si-O-Si, and Al-O-Al linkages. The aluminum centers are negatively charged, which requires an accompanying cation.
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