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Synthesis reactions elements

The abundances in the Earth s crust of both the d-block transition metals and the f-block inner transition metals vary considerably, as shown in Table 1.2. Iron is the most common of the transition metals (6.30% by mass of the crustal rocks) and this reflects the high yield of iron from element synthesis reactions in stellar supernovae. Titanium (0.66%) and manganese (0.11%) are also quite abundant, but some of the heavier... [Pg.5]

Titanium Dibromide. Titanium dibromide [13873-04-5] a black crystalline soHd, density 4310 kg/m, mp 1025°C, has a cadmium iodide-type stmcture and is readily oxidized to trivalent titanium by water. Spontaneously flammable in air (142), it can be prepared by direct synthesis from the elements, by reaction of the tetrabromide with titanium, or by thermal decomposition of titanium tribromide. This last reaction must be carried out either at or below 400°C, because at higher temperatures the dibromide itself disproportionates. [Pg.131]

ZrSe [12166-53-9] and ZrTe [39294-10-5] (138). Zirconium disulfide [12039-15-5] is made from the elemental powders and by the action of carbon disulfide on zirconium oxide above 1200°C (139) some ZrOS [12164-95-3] is usually also obtained. The higher sulfides disproportionate at ca 700°C synthesis reactions at 900—1000°C with S Zr ratios between 0.2 and 2.3 produced crystals that were identified as Zr S2 [12595-12-9] ... [Pg.434]

The earliest method for manufacturiag carbon disulfide involved synthesis from the elements by reaction of sulfur and carbon as hardwood charcoal in externally heated retorts. Safety concerns, short Hves of the retorts, and low production capacities led to the development of an electric furnace process, also based on reaction of sulfur and charcoal. The commercial use of hydrocarbons as the source of carbon was developed in the 1950s, and it was still the predominate process worldwide in 1991. That route, using methane and sulfur as the feedstock, provides high capacity in an economical, continuous unit. Retort and electric furnace processes are stiU used in locations where methane is unavailable or where small plants are economically viable, for example in certain parts of Africa, China, India, Russia, Eastern Europe, South America, and the Middle East. Other technologies for synthesis of carbon disulfide have been advocated, but none has reached commercial significance. [Pg.29]

Elemental Huonne as a Legitimate Reagent for Selective Fluonnation of Orgamc Compounds Fluoroaromatic Compounds Synthesis, Reactions, and Commercial Applications New Aspects of Carbonylations Catalyzed by Transition Metal Complexes Polyfluoroaromatics An Excursion m Carbamon Chemistry ... [Pg.19]

The production of ammonia is of historical interest because it represents the first important application of thermodynamics to an industrial process. Considering the synthesis reaction of ammonia from its elements, the calculated reaction heat (AH) and free energy change (AG) at room temperature are approximately -46 and -16.5 KJ/mol, respectively. Although the calculated equilibrium constant = 3.6 X 108 at room temperature is substantially high, no reaction occurs under these conditions, and the rate is practically zero. The ammonia synthesis reaction could be represented as follows ... [Pg.144]

The aim of this review is to focus on the hydrogen bonding, the acidity and basicity, complexing as well as some aspects of computational chemistry concerning the organo-element chemistry of germanium, tin and lead. This chapter is not exhaustive in scope, but rather consists of surveys of the most recent decade of work in this still developing area. This chapter emphasizes the synthesis, reactions and molecular structures of the class of... [Pg.538]

In a synthesis reaction involving elements A and B, the oxidation number of element A increases. What happens to the oxidation number of element B How do you know ... [Pg.500]

Write a balanced equation for a synthesis reaction in which elemental oxygen acts as a reducing agent. [Pg.500]

Summarizing, there are still many scientific challenges and major opportunities for the catalysis community in the field of cobalt-based Fischer-Tropsch synthesis to design improved or totally new catalyst systems. However, such improvements require a profound knowledge of the promoted catalyst material. In this respect, detailed physicochemical insights in the cobalt-support, cobalt-promoter and support-support interfacial chemistry are of paramount importance. Advanced synthesis methods and characterization tools giving structural and electronic information of both the cobalt and the support element under reaction conditions should be developed to achieve this goal. [Pg.42]

The remainder of the Fowler article is of great interest, but in detail that is beyond the scope of this encyclopedia. Topics covered by Fowler include early research on element synthesis stellar reaction rates from laboratory cross sections hydrogen burning in main-sequence stars and the solar neutrino problem synthesis of l3C and, 60 and... [Pg.329]

The synthesis reactions used to discover the transuranium elements are given in Table 15.2. All these reactions are complete fusion reactions in which the reacting nuclei fuse, equilibrate, and deexcite in a manner independent of their mode of formation. Other production reactions involving a partial capture of the projectile nucleus are also possible. [Pg.433]

Aside on Element Synthesis Calculations The reactions used to synthesize heavy nuclei are, quite often, very improbable reactions, representing minor branches to the main reaction. Their probability of occurrence with respect to the main synthesis... [Pg.435]

Fig. 5.4 depicts some results obtained in the first stages (high nuclearity complexes formation) of the synthesis in xylene solvent which leads to the formation of nanostructured powders, RuxSey, from tris-ruthenium dodeca-carbonyl (Ru3(CO)i2) and elemental selenium dissolved in an organic solvent (xylene). After 40 minutes of reaction, l3C-NMR spectrum (Fig. 5.4 (c)) puts in evidence the formation of a new polynuclear chemical precursor with a chemical shift 8 of 198.89 ppm (i.e., Ru4Se2(CO)n)- Selenium takes part in the coordination sphere. The peak intensity with the chemical shift of 199.67 ppm, corresponds to the initial chemical precursor which decreases as a function of the synthesis reaction time (Fig. 5.4(a)). Other chemical shifts (with minor peak intensities) on both sides of the 13C-NMR spectrum, which put in evidence the complex interplay of the reaction, are also observed. [Pg.139]

In a synthesis reaction, two or more elements or compounds combine to form a new substance. Synthesis reactions are also known as combination or formation reactions. A general equation for a synthesis reaction is... [Pg.120]

In a simple synthesis reaction, one element reacts with one or more other elements to form a compound. Two, three, four, or more elements may react to form a single product, although synthesis reactions involving four or more reactants are extremely rare. Why do you think this is so When two elements react together, the reaction is almost always a synthesis reaction because the product is almost always a single compound. There are several types of synthesis reactions. Recognizing the patterns of the various types of reactions will help you to predict whether substances will take part in a synthesis reaction. [Pg.120]

In the previous two types of synthesis reactions, two elements reacted to form one product. There are many synthesis reactions in which one or more compounds are the reactants. For the purpose of this course, however, we will deal only with the two specific types of synthesis reactions involving compounds that you should recognize oxides and water. [Pg.121]

In a decomposition reaction, a compound breaks down into elements or other compounds. Therefore, a decomposition reaction is the opposite of a synthesis reaction. A general formula for a decomposition reaction is ... [Pg.122]

Compounds that contain elements other than carbon also undergo complete combustion to form stable oxides. For instance, sulfur-containing compounds undergo combustion to form sulfur dioxide, S02, a precursor to acid rain. Complete combustion reactions are often also synthesis reactions. Metals, such as magnesium, undergo combustion to form their most stable oxide, as shown in Figure 4.11. [Pg.124]

In practice, you can determine a compound s empirical formula by analyzing its percentage composition. There are several different ways to do this. One way is to use a synthesis reaction in which a sample of an element with a known mass reacts with another element to form a compound. Since you know the mass of one of the elements and you can measure the mass of the compound produced, you can calculate the percentage composition. [Pg.211]

For the preparation of RE-POM complexes, traditional aqueous solution synthesis and hydrothermal synthesis [2] are the two main synthetic methods. In traditional aqueous solution synthesis, reactions are carried out in the temperature range from room temperature to the boiling point of water, and in general start from plenary or lacunary POMs and simple RE salts. Hydrothermal reactions typically proceed in the temperature range 120-200 C under autogenous pressure, and usually use simple metal salts of all the required elements as the starting materials. As different solubility problems are minimized under hydrothermal conditions, the... [Pg.193]

The following discussion concentrates mainly on the ammonia synthesis reaction over iron catalysts and refers only briefly to reactions with non-iron catalysts. Iron catalysts which are generally used until today in commercial production units are composed in unreduced form of iron oxides (mainly magnetite) and a few percent of Al, Ca, and K other elements such as Mg and Si may also be present in small amounts. Activation is usually accomplished in situ by reduction with synthesis gas. Prereduced catalysts are also commercially available. [Pg.23]


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