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Siliceous earths properties

Oxygen is the most abundant element on earth. The earth s crust is rich in carbonate and silicate rocks, the oceans are almost entirely water, and oxygen constitutes almost one fifth of the air we breathe. Carbon ranks only fourteenth among the elements in natural abundance, but trails only hydrogen and oxygen in its abundance in the human body. It is the chemical properties of carbon that make it uniquely suitable as the raw material forthe building blocks of life. Let s find out more about those chemical properties. [Pg.6]

As a result of its unique chemical and physical properties, silica gel is probably the most important single substance involved in liquid chromatography today. Without silica gel, it is doubtful whether HPLC could have evolved at all. Silica gel is an amorphous, highly porous, partially hydrated form of silica which is a substance made from the two most abundant elements in the earth s crust, silicon and oxygen. Silica, from which silica gel is manufactured, occurs naturally, either in conjunction with metal oxides in the form of silicates, such as clay or shale, or as free silica in the form of quartz, cristobalite or tridymite crystals. Quartz is sometimes found clear and colorless, but more often in an opaque form, frequently colored... [Pg.55]

Antiblock additives are often incorporated into packaging films to prevent them sticking together. Their effectiveness relates directly to the roughness they impart on a film surface while minimising loss in optical properties. They are often used in association with slip additives such as erucamide. Common antiblock additives include crystalline silica, diatomaceous earth and talc (magnesium silicate). [Pg.573]

The two rare earth elements niobium (Nb) and tantalum (Ta) were the main subject of study in the investigation referred to. Both elements have very similar properties and almost always occur together in our solar system. However, the silicate crust of the Earth contains around 30% less niobium (compared to its sister tantalum). Where are the missing 30% of niobium They must be in the Earth s FeNi core. It is known that the metallic core can only take up niobium under huge pressures, and the conditions necessary for this may have been present on Earth. Analyses of meteorites from the asteroid belt and from Mars show that these do not have a niobium deficit. [Pg.30]

These can be inorganic materials such as calcium silicate, mineral wool, diatomaceous earth or perlite and mineral wool. If provided as an assembly they are fitted with steel panels or jackets. These are woven noncombustible or flame retardant materials the provide insulation properties to fire barrier for the blockage of heat transfer. [Pg.169]

Among the precipitants employed were tannic acid, tartar emetic, rosin soaps, fatty acid (stearic, oleic) soaps, sulphonated oils (Turkey red oil), earth lakes (mixed natural silicates), phosphates, casein and arsenious acid. The fastness properties of these pigments... [Pg.46]

Abstracting from the complexity of the real systems, there is one common property of all natural particles. Their surfaces contain functional groups which can interact with H+, OH and metal ions and - if Lewis acid sites, e.g., =AI and =Fe, are available on the surface - with ligands. Many inorganic solids (oxidesQand silicates) contain hydroxo groups carbonates and sulfides expose -C-oh,-c oh, MeOH and -SH groups, respectively. While the interaction of alkaline and earth-alkaline ions... [Pg.369]

The study of coordination compounds of the lanthanides dates in any practical sense from around 1950, the period when ion-exchange methods were successfully applied to the problem of the separation of the individual lanthanides,131-133 a problem which had existed since 1794 when J. Gadolin prepared mixed rare earths from gadolinite, a lanthanide iron beryllium silicate. Until 1950, separation of the pure lanthanides had depended on tedious and inefficient multiple crystallizations or precipitations, which effectively prevented research on the chemical properties of the individual elements through lack of availability. However, well before 1950, many principal features of lanthanide chemistry were clearly recognized, such as the predominant trivalent state with some examples of divalency and tetravalency, ready formation of hydrated ions and their oxy salts, formation of complex halides,134 and the line-like nature of lanthanide spectra.135... [Pg.1068]

The natural clay minerals are hydrous aluminum silicates with iron or magnesium replacing aluminum wholly or in part, and with alkali or alkaline earth metals present as essential constituents in some others. Their acidic properties and natural abundance have favored their use as catalysts for cracking of heavy petroleum fractions. With the exception of zeolites and some specially treated mixed oxides for which superacid properties have been claimed, the acidity as measured by the color changes of absorbed Hammett bases is generally far below the superacidity range. They are inactive for alkane isomerization and cracking below 100 °C and need co-acids to reach superacidity. [Pg.68]

Clay minerals and clay colloids are the products of the advanced weathering of primary silicates. They are comprised mainly of silica and alumina, often with appreciable amounts of alkali and alkaline earth metals and iron. Most also have varying amounts of water bound to their surfaces and can take on a variety of different chemical and physical properties depending on the amount of water adsorbed. They have the ability to exchange or bind cations and anions and are capable of complex formation with a wide variety of organic molecules. [Pg.116]


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See also in sourсe #XX -- [ Pg.328 ]




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Siliceous earth

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