To use all functions of this page, please activate cookies in your browser.
With an accout for my.chemeurope.com you can always see everything at a glance – and you can configure your own website and individual newsletter.
- My watch list
- My saved searches
- My saved topics
- My newsletter
Zeolites (Greek, zein, "to boil"; lithos, "a stone") are minerals that have a micro-porous structure. The term was originally coined in the 18th century by a Swedish mineralogist named Axel Fredrik Cronstedt who observed, upon rapidly heating a natural mineral, that the stones began to dance about as the water evaporated. Using the Greek words which mean "stone that boils," he called this material zeolite.
More than 150 zeolite types have been synthesized and 48 naturally occurring zeolites are known. They are basically hydrated alumino-silicate minerals with an "open" structure that can accommodate a wide variety of cations, such as Na+, K+, Ca2+, Mg2+ and others. These positive ions are rather loosely held and can readily be exchanged for others in a contact solution. Some of the more common mineral zeolites are: analcime, chabazite, heulandite, natrolite, phillipsite, and stilbite. An example mineral formula is: Na2Al2Si3O10-2H2O, the formula for natrolite.
Natural zeolites form where volcanic rocks and ash layers react with alkaline groundwater. Zeolites also crystallized in post-depositional environments over periods ranging from thousands to millions of years in shallow marine basins. Naturally occurring zeolites are rarely pure and are contaminated to varying degrees by other minerals, metals, quartz or other zeolites. For this reason, naturally occurring zeolites are excluded from many important commercial applications where uniformity and purity are essential.
Zeolites are the aluminosilicate members of the family of microporous solids known as "molecular sieves". The term molecular sieve refers to a particular property of these materials, i.e. the ability to selectively sort molecules based primarily on a size exclusion process. This is due to a very regular pore structure of molecular dimensions. The maximum size of the molecular or ionic species that can enter the pores of a zeolite is controlled by the diameters of the tunnels. These are conventionally defined by the ring size of the aperture, where, for example, the term "8ring" refers to a closed loop that is built from 8 tetrahedrally coordinated silicon (or aluminium) atoms and 8 oxygen atoms. These rings are not always perfectly flat and symmetrical due to a variety of effects, including strain induced by the bonding between units that are needed to produce the overall structure, or coordination of some of the oxygen atoms of the rings to cations within the structure. Therefore, the pore openings for all rings of one size are not identical.
Additional recommended knowledge
Conventional open pit mining techniques are used to mine natural zeolites. The overburden is removed to allow access to the ore. The ore may be blasted or stripped for processing by using tractors equipped with ripper blades and front-end loaders. In processing, the ore is crushed, dried, and milled. The milled ore may be air-classified as to particle size and shipped in bags or bulk. The crushed product may be screened to remove fine material when a granular product is required, and some pelletized products are produced from fine material. Producers also may modify the properties of the zeolite or blend their zeolite products with other materials before sale to enhance their performance.
Currently, the world’s annual production of natural zeolite is about 4 million tons. Of this quantity, 2.6 million tons are shipped to Chinese markets to be used in the concrete industry. Eastern Europe, Western Europe, Australia, and Asia are world leaders in supplying the world’s demand for natural zeolite. By comparison, only 57,400 metric tons (source: U.S. Geological Survey, 2004) of zeolite (only 1% of the world’s current production) is produced in North America; only recently has North America realized the potential for current and future markets.
There are several types of synthetic zeolites that form by a process of slow crystallization of a silica-alumina gel in the presence of alkalis and organic templates. One of the important processes used to carry out zeolite synthesis is sol-gel processing. The product properties depend on reaction mixture composition, pH of the system, operating temperature, pre-reaction 'seeding' time, reaction time as well as the templates used. In sol-gel process, other elements (metals, metal oxides) can be easily incorporated. The silicalite sol formed by the hydrothermal method is very stable. Also the ease of scaling up this process makes it a favorite route for zeolite synthesis.
Synthetic zeolites hold some key advantages over their natural analogs. The synthetics can, of course, be manufactured in a uniform, phase-pure state. It is also possible to manufacture desirable zeolite structures which do not appear in nature. Zeolite A is a well-known example. Since the principal raw materials used to manufacture zeolites are silica and alumina, which are among the most abundant mineral components on earth, the potential to supply zeolites is virtually unlimited. Finally, zeolite manufacturing processes engineered by man require significantly less time than the 50 to 50,000 years prescribed by nature. Disadvantages include the inability to create crystals with dimensions of a comparable size to their natural counterparts.
Commercial and Domestic
Zeolites are widely used as ion-exchange beds in domestic and commercial water purification, softening, and other applications. In chemistry, zeolites are used to separate molecules (only molecules of certain sizes and shapes can pass through), as traps for molecules so they can be analyzed.
Zeolites have the potential of providing precise and specific separation of gases including the removal of H2O, CO2 and SO2 from low-grade natural gas streams. Other separations include: noble gases, N2, freon and formaldehyde. However at present, the true potential to improve the handling of such gases in this manner remains unknown.
Synthetic zeolites are widely used as catalysts in the petrochemical industry, for instance in fluid catalytic cracking and hydro-cracking. Zeolites confine molecules in small spaces, which causes changes in their structure and reactivity. The hydrogen form of zeolites (prepared by ion-exchange) are powerful solid-state acids, and can facilitate a host of acid-catalyzed reactions, such as isomerisation, alkylation, and cracking. Catalytic cracking uses a furnace and reactor. First crude oil distillation fractions are heated in the furnace and passed to the reactor. In the reactor the crude meets with a catalyst such as zeolite. It goes through this step three times, each time getting cooler. Finally it reaches a step known as separator. The separator collects recycled hydrogen. Then it goes through a fractionator and becomes the final item.
Zeolites have uses in advanced reprocessing methods, where their micro-porous ability to capture some ions while allowing others to pass freely allow many fission products to be efficiently removed from nuclear waste and permanently trapped. Equally important are the mineral properties of zeolites. Their alumino-silicate construction is extremely durable and resistant to radiation even in porous form. Additionally, once they are loaded with trapped fission products, the zeolite-waste combination can be hot pressed into an extremely durable ceramic form, closing the pores and trapping the waste in a solid stone block. This is a waste form factor that greatly reduces its hazard compared to conventional reprocessing systems. 
In agriculture, clinoptilolite (a naturally occurring zeolite) is used as a soil treatment. It provides a source of slowly released potassium. If previously loaded with ammonium, the zeolite can serve a similar function in the slow release of nitrogen. Cuban studies in the emerging field of "zeoponics" suggest that some crops may be grown in 100% zeolite or zeolite mixtures in which the zeolite is previously loaded or coated with fertilizer and micronutrients. Zeolites can also act as water moderators, in which they will absorb up to 55% of their weight in water and slowly release it under plant demand. This property can prevent root rot and moderate drought cycles.
A potting soil with 12% clinoptilolite was shown to harvest morning dew and return it to the plant roots for reuse. The same bed was able to grow a Jerico strain of leaf lettuce in a sub tropical climate without external water and daytime temperatures exceeding 85 °F. This produce did not bolt and went full term before setting seeds. It also has been shown that certain zeolites can reduce nitrates and nitrites to more plant usable free nitrogen by ion exchange.
In Concentrated Animal Growing facilities, the addition of as little as 1% of a very low sodium clinoptiloite was shown to improve feed conversion, reduce airborne ammonia up to 80%, act as a mycotoxin binder and improve bone density. See US Patents 4,917,045 and 6,284,232. Can be used in general odor elimination for all animal odors.
Zeolite-based oxygen generation systems are widely used to produce medical grade oxygen. The zeolite is used as a molecular sieve to create purified oxygen from air, in a process involving the absorption of undesired gases and other atmospheric components, leaving highly purified oxygen and up to 5% argon. Zeolite is also the active component in QuikClot, an emergency coagulant.
Heating and refrigeration
Zeolites can be used as solar thermal collectors and for adsorption refrigeration. In these applications, their high heat of adsorption and ability to hydrate and dehydrate while maintaining structural stability is exploited. This hygroscopic property coupled with an inherent exothermic reaction when transitioning from a dehydrated to a hydrated form (heat adsorption), make natural zeolites effective in the storage of solar and waste heat energy.
The largest outlet for synthetic zeolite is the global laundry detergent market. This amounted to 1.44 million metric tons per year of anhydrous zeolite A in 1992.
Synthetic zeolite is also being used as an additive in the production process of warm mix asphalt concrete. The development of this application started in Europe (Germany) in the 1990s. It helps by decreasing the temperature level during manufacture and laying of asphalt concrete, resulting in lower consumption of fossil fuels, thus releasing less carbon dioxide, aerosols and vapours. Other than that the usage of synthetic zeolite in hot mixed asphalt leads to easier compaction and to a certain degree allows cold weather paving and longer hauls.
Thomsonites, one of the rarer zeolite minerals, have been collected as gemstones from a series of lava flows along Lake Superior in Minnesota and to a lesser degree in Michigan, U.S.A.. Thomsonite nodules from these areas have eroded from basalt lava flows and are collected on beaches and by scuba divers in Lake Superior.
These thomsonite nodules have concentric rings in combinations of colors, black, white, orange, pink, red and many shades of green. Some nodules have copper as inclusions and rarely will be found with copper "eyes". When polished by a lapidary the thomsonites sometimes display chatoyancy.
Zeolites are marketed by pet stores for use as a filter additive in aquariums. In aquariums, zeolites can be used to absorb ammonia and other nitrogenous compounds. However, due to the high affinity of some zeolites for calcium, they may be less effective in hard water and may deplete calcium. Zeolite filtration is used in some marine aquaria to keep nutrient concentrations low for the benefit of corals adapted to nutrient-depleted waters.
Space hardware testing
Zeolite can be used as a molecular sieve in cryosorption pumps for rough pumping of vacuum chambers which can be used to simulate space-like conditions in order to test hardware bound for space.
Zeolite mineral species
The Zeolite family includes
Frederick A. Mumpton. National Academy of Sciences Vol. 96, Issue 7, 3463-3470, March 30, 1999 Abstract
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Zeolite". A list of authors is available in Wikipedia.|