Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sulfur dioxide main processes

The sulfone is a versatile functional group comparable to the carbonyl functionality in its ability to activate molecules for further bond construction, the main difference between these two groups being that the sulfone is usually removed once the synthetic objective is achieved. The removal most commonly involves a reductive desulfonylation process with either replacement of the sulfone by hydrogen (Eq. 1), or a process that results in the formation of a carbon-carbon multiple bond when a P-functionalized sulfone, for example a (3-hydroxy or (3-alkoxy sulfone, is employed (Eq. 2). These types of reactions are the Julia-Lythgoe or Julia-Paris-Kocienski olefination processes. Alkylative desulfonylation (substitution of the sulfone by an alkyl group, Eq. 3), oxidative desulfonylation (Eq. 4), and substitution of the sulfone by a nucleophile (nucleophilic displacement, Eq. 5) are also known. Finally, p-eliminations (Eq. 6) or sulfur dioxide extrusion processes (Eqs. 7, 8 and 9) have become very popular for the... [Pg.372]

Solvent Treatment. Solvent processes can be divided into two main categories, solvent extraction and solvent dewaxing. The solvent used in the extraction processes include propane and cresyHc acid, 2,2 -dichlorodiethyl ether, phenol (qv), furfural, sulfur dioxide, benzene, and nitrobenzene. In the dewaxing process (28), the principal solvents are benzene, methyl ethyl ketone, methyl isobutyl ketone, propane, petroleum naphtha, ethylene dichloride, methylene chloride, sulfur dioxide, and iV-methylpyrroHdinone. [Pg.208]

Paper Products. Paper (qv) products account for about 2% of sulfur demand. The largest single segment of demand is in the manufacture of wood pulp by the sulfite process (see Pulp). In this process, the main sulfur intermediate is sulfur dioxide, which is generally produced at the plant site by burning elemental sulfur. Some sulfur dioxide, however, is produced as a by-product at smelter operations, purified andUquefied, and shipped to the pulp mills. The sulfur dioxide is converted to sulfurous acid, and the salt of this acid is a principal component of the cooking Hquor for the sulfite process. [Pg.125]

Roasting. Copper and lead sulfides are direcdy smelted but not zinc sulfide. However, theoretical calculations are encouraging (20) and, if an efficient means of condensing zinc rapidly from 1600 K in the presence of carbon dioxide, sulfur dioxide, and steam can be devised, the process may be feasible. The reaction of zinc vapor to yield zinc oxide or zinc sulfide presents the main difficulty. [Pg.399]

The most efficient processes in Table I are for steel and alumintim, mainly because these metals are produced in large amounts, and much technological development has been lavished on them. Magnesium and titanium require chloride intermediates, decreasing their efficiencies of production lead, copper, and nickel require extra processing to remove unwanted impurities. Sulfide ores produce sulfur dioxide (SO2), a pollutant, which must be removed from smokestack gases. For example, in copper production the removal of SO, and its conversion to sulfuric acid adds up to 8(10) JA g of additional process energy consumption. In aluminum production disposal of waste ciyolite must be controlled because of possible fiuoride contamination. [Pg.772]

Liquid solvents are used to extract either desirable or undesirable compounds from a liquid mixture. Solvent extraction processes use a liquid solvent that has a high solvolytic power for certain compounds in the feed mixture. For example, ethylene glycol has a greater affinity for aromatic hydrocarbons and extracts them preferentially from a reformate mixture (a liquid paraffinic and aromatic product from catalytic reforming). The raffinate, which is mainly paraffins, is freed from traces of ethylene glycol by distillation. Other solvents that could be used for this purpose are liquid sulfur dioxide and sulfolane (tetramethylene sulfone). [Pg.53]

This process includes two main sections the burner section with a reaction chamber that does not have a catalyst, and a Claus reactor section. In the burner section, part of the feed containing hydrogen sulfide and some hydrocarbons is burned with a limited amount of air. The two main reactions that occur in this section are the complete oxidation of part of the hydrogen sulfide (feed) to sulfur dioxide and water and the partial oxidation of another part of the hydrogen sulfide to sulfur. The two reactions are exothermic ... [Pg.116]

FIGURE 44 Weathering. A weathered sandstone column. Calcite (composed of calcium carbonate) is dissolved by rain and groundwater (see Textbox 73). When stone in which calcite is a main component as, for example, sandstone, limestone, and marble, is in contact with water for long periods of time, it is weathered and partly or entirely dissolved. Pollutants such as sulfur dioxide are fundamental in accelerating the weathering and dissolution process. When sulfur dioxide, for example, dissolves in rainwater, it forms sulfuric acid, a strong acid that, at ambient temperatures, rapidly dissolves calcium carbonate. [Pg.234]

Outokumpu [Named after a hill in Finland, near Kuusjarvi] A flash-smelting process for sulfide ores, ft is an energy-efficient process (also called an autogenous process), using mainly the heat of combustion of the contained sulfur to sulfur dioxide, rather than ary external source of heat. Developed R Bryk and J. Ryselin at the Haijavalta works of Outokumpu Oy, Finland, in 1946. Used mainly for copper ores, but also for nickel, iron, and lead by 1988, 40 plants were using the process worldwide. [Pg.198]

This is a process mainly used in power plants for reduction of hexavalent chromium to bivalent chromium. Sulfur dioxide, sodium bisulfite, sodium metabisulfite, and ferrous salts are common reducing agents to be used in the process. A pH range of 2-3 should be controlled. The process efficiency of removal is about 99.7%. [Pg.611]

The physical properties of charcoal-type materials are mainly determined by the nature and magnitude of their surface areas. In finely divided forms, vast surfaces are presented with only partially saturated attractive forces, thereby absorbing large amounts of gases and vapours, including appreciable quantities of sulfur dioxide, an important process during the combustion of gunpowder. [Pg.19]

It is also doubtful that the industry will be in a position for many years to come to undertake sulfur removal from residual fuels solely to improve product quality. A number of consumer industries demand low sulfur fuel oils, but these special requirements can at present be met more appropriately by selection of crude rather than by adoption of desulfurization processes. In general industrial use, it is corrosion and atmospheric pollution that are the main disadvantages of high sulfur content. But there is no sign yet of the development of a cheap desulfurization process, the cost of which can be substantially offset by the gain in efficiency resulting from permissible lower stack temperatures or by the elimination of flue gas scrubbing equipment previously necessary for reduction of sulfur dioxide content. [Pg.159]

Popcorn polymers are hard, brittle, highly crosslinked porous masses, named as such because of their physical appearance. The formation of popcorn polymers in industrial polymerization processes is highly undesirable. The formation can be suppressed by suitable crosslinking inhibitors. However, in order to avoid the formation on the walls of a reactor that are mainly in contact with the gas phase, volatile crosslinking inhibitors must be chosen. Examples for volatile crosslinking inhibitors are nitric oxide and sulfur dioxide (15,16). [Pg.302]

While hexavalent chromium is reduced to its trivalent form in treatment systems mainly so that the metal can be precipitated, this also lowers its toxicity by a factor of 1000. Ferrous sulfate can be used for this reduction, but is not popular due to its inefficiency, high sludge generation rate, and expense. Sulfur dioxide gas is a far more economical reducing agent, although it is efficient only at low pH, preferably below 2. There can also be problems with atmospheric emission of S02 in this process. [Pg.67]

Since this estimated share pattern was derived mainly from projection of trends (particularly long term trends), it seems appropriate to focus on oil and speculate as to how possible future events might alter its forecast future role. Events related to pollution control tend to indicate increases in petroleum demand. The use of lead free gasoline, for instance, requires additional refinery processing, which in turn consumes more petroleum fuel. Increasingly tighter controls on sulfur dioxide emissions from thermal-electric plants will cause a shift from coal to low sulfur fuel oil if there is no economic flue-gas desulfurization to cope with coals sulfur content. [Pg.227]

The addition of thiols to C—C multiple bonds may proceed via an electrophilic pathway involving ionic processes or a free radical chain pathway. The main emphasis in the literature has been on the free radical pathway, and little work exists on electrophilic processes.534-537 The normal mode of addition of the relatively weakly acidic thiols is by the electrophilic pathway in accordance with Markovnikov s rule (equation 299). However, it is established that even the smallest traces of peroxide impurities, oxygen or the presence of light will initiate the free radical mode of addition leading to anti-Markovnikov products. Fortunately, the electrophilic addition of thiols is catalyzed by protic acids, such as sulfuric acid538 and p-toluenesulfonic acid,539 and Lewis acids, such as aluminum chloride,540 boron trifluoride,536 titanium tetrachloride,540 tin(IV) chloride,536 540 zinc chloride536 and sulfur dioxide.541... [Pg.316]

National Dust Collector, developed a process based on dry limestone injection in the boiler. By 1972, the Combustion Engineering process had been installed on five boilers, but these installations proved inadequate owing mainly to boiler plugging, low sulfur dioxide absorption, and reduced particulate collection efficiency in the electrostatic precipitator. [Pg.153]


See other pages where Sulfur dioxide main processes is mentioned: [Pg.346]    [Pg.543]    [Pg.453]    [Pg.275]    [Pg.115]    [Pg.117]    [Pg.443]    [Pg.916]    [Pg.449]    [Pg.916]    [Pg.356]    [Pg.86]    [Pg.948]    [Pg.434]    [Pg.435]    [Pg.457]    [Pg.490]    [Pg.159]    [Pg.88]    [Pg.264]    [Pg.410]    [Pg.432]    [Pg.465]    [Pg.8]    [Pg.115]    [Pg.117]    [Pg.158]    [Pg.35]    [Pg.846]    [Pg.111]    [Pg.347]   
See also in sourсe #XX -- [ Pg.505 ]




SEARCH



Sulfur dioxide processes

© 2024 chempedia.info