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Sulfur dioxide combustion

CSTR for most reactions. These conditions are best met for short residence times where velocity profiles in the tubes can be maintained in the turbulent flow regime. In an empty tube this requires high flow rates for packed columns the flow rates need not be as high. Noncatalytic reactions performed in PFRs include high-pressure polymerization of ethylene and naphtha conversion to ethylene. A gas-liquid noncatalytic PFR is used for adipinic nitrile production. A gas-solid PFR is a packed-bed reactor (Section IV). An example of a noncatalytic gas-solid PFR is the convertor for steel production. Catalytic PFRs are used for sulfur dioxide combustion and ammonia synthesis. [Pg.466]

Chlorates Ammonium salts, acids, metal powders, sulfur, flnely divided organic or combustible materials, cyanides, metal sulfldes, manganese dioxide, sulfur dioxide, organic acids... [Pg.1207]

When a suitable reaction involving the analyte does not exist it may be possible to generate a species that is easily titrated. Eor example, the sulfur content of coal can be determined by using a combustion reaction to convert sulfur to sulfur dioxide. [Pg.275]

Formation of emissions from fluidised-bed combustion is considerably different from that associated with grate-fired systems. Flyash generation is a design parameter, and typically >90% of all soHds are removed from the system as flyash. SO2 and HCl are controlled by reactions with calcium in the bed, where the lime-stone fed to the bed first calcines to CaO and CO2, and then the lime reacts with sulfur dioxide and oxygen, or with hydrogen chloride, to form calcium sulfate and calcium chloride, respectively. SO2 and HCl capture rates of 70—90% are readily achieved with fluidi2ed beds. The limestone in the bed plus the very low combustion temperatures inhibit conversion of fuel N to NO. ... [Pg.58]

The furnace is constmcted with a steel shell lined with high temperature refractory (see Refractories). Refractory type and thickness are deterrnined by the particular need. Where combustion products include corrosive gases such as sulfur dioxide or hydrogen chloride, furnace shell temperatures are maintained above about 150—180°C to prevent condensation and corrosion on the inside carbon steel surfaces. Where corrosive gases are not present, insulation is sized to maintain a shell temperature below 60°C to protect personnel. [Pg.54]

A smaller factor in ozone depletion is the rising levels of N2O in the atmosphere from combustion and the use of nitrogen-rich fertilizers, since they ate the sources of NO in the stratosphere that can destroy ozone catalyticaHy. Another concern in the depletion of ozone layer, under study by the National Aeronautics and Space Administration (NASA), is a proposed fleet of supersonic aircraft that can inject additional nitrogen oxides, as weU as sulfur dioxide and moisture, into the stratosphere via their exhaust gases (155). Although sulfate aerosols can suppress the amount of nitrogen oxides in the stratosphere... [Pg.503]

L. B. Heia, A. B. Phillips, and R. D. Young, "Recovery of Sulfur Dioxide from Coal Combustion Stack Gases," ia F. S. MaHette, ed. Problems and Control of A.ir Pollution, Reioliold Publishing Corporation, New York, 1955, pp. 155—169. [Pg.369]

Analytical Methods. Detection of carbonyl sulfide ia air can be done by gas chromatography or by combustion to sulfur dioxide and determination of the latter. Where hydrogen sulfide and carbonyl sulfide occur together, the carbonyl sulfide can be determined by combustion after hydrogen sulfide is absorbed by lead acetate, which does not absorb carbonyl sulfide (35). [Pg.130]

Combustion of Sulfur. For most chemical process appHcations requiring sulfur dioxide gas or sulfurous acid, sulfur dioxide is prepared by the burning of sulfur or pyrite [1309-36-0], FeS2. A variety of sulfur and pyrite burners have been developed for sulfuric acid and for the pulp (qv) and paper (qv) iadustries, which produce and immediately consume about 90% of the captive sulfur dioxide produced ia the United States. Information on the European sulfur-to-sulfuric acid technology (with emphasis on Lurgi) is available (255). [Pg.145]

A basic research study on combustion of sulfur led to the postulation that sulfur trioxide may actually be the primary combustion product and that sulfur dioxide may then be produced by the further reaction of sulfur trioxide with sulfur vapor ki the oxygen-deficient region of the flame (261). [Pg.146]

Chemical Properties. Anhydrous sodium dithionite is combustible and can decompose exothermically if subjected to moisture. Sulfur dioxide is given off violentiy if the dry salt is heated above 190°C. At room temperature, in the absence of oxygen, alkaline (pH 9—12) aqueous solutions of dithionite decompose slowly over a matter of days. Increased temperature dramatically increases the decomposition rate. A representation of the decomposition chemistry is as follows ... [Pg.150]

The Claus process converts hydrogen sulfide to elemental sulfur via a two-step reaction. The first step involves controUed combustion of the feed gas to convert approximately one-third of the hydrogen sulfide to sulfur dioxide (eq. 9) and noncatalytic reaction of unbumed hydrogen sulfide with sulfur dioxide (eq. 10). In the second step, the Claus reaction, the hydrogen sulfide and sulfur dioxide react over a catalyst to produce sulfur and water (eq. 10). The principal reactions are as foUow ... [Pg.212]

The amount of combustion ait is tightly controlled to maximize sulfur recovery, ie, maintaining the appropriate reaction stoichiometry of 2 1 hydrogen sulfide to sulfur dioxide throughout downstream reactors. Typically, sulfur recoveries of up to 97% can be achieved (7). The recovery is heavily dependent on the concentration of hydrogen sulfide and contaminants, especially ammonia and heavy hydrocarbons, ia the feed to the Claus unit. [Pg.213]

New flash roasters dry on the bottom hearth the ore is introduced in two opposed burners for increased turbulence (24). Such roasters with combustion chambers of 8—9 m high are capable of dead roasting (sulfide removal to <0.5%) over 300 t of zinc concentrates per day with 10% sulfur dioxide in the off-gas. [Pg.399]

Hot surfaces and electric sparks are potential ignition sources for carbon disulfide. The ignition temperature depends on specific conditions, and values from 90 to 120°C in air have been reported (2,22). Data on carbon disulfide oxidation and combustion have been summarized (18). Oxidation products ate generally sulfur dioxide [7446-09-5] and carbon dioxide [124-58-9J ... [Pg.27]

Flame Temperature. The adiabatic flame temperature, or theoretical flame temperature, is the maximum temperature attained by the products when the reaction goes to completion and the heat fiberated during the reaction is used to raise the temperature of the products. Flame temperatures, as a function of the equivalence ratio, are usually calculated from thermodynamic data when a fuel is burned adiabaticaHy with air. To calculate the adiabatic flame temperature (AFT) without dissociation, for lean to stoichiometric mixtures, complete combustion is assumed. This implies that the products of combustion contain only carbon dioxide, water, nitrogen, oxygen, and sulfur dioxide. [Pg.517]

Fluidized beds are ideal for the combustion of high sulfur coals since the sulfur dioxide produced by combustion reacts with the introduced calcined limestone to produce calcium sulfate. The chemistry involved can be simplified and reduced to two steps, calcination and sulfation. [Pg.526]

Sulfur dioxide Fuel combustion (coal, oil), smelting and casting, manufacture of paper by sulfite process Primary metals (ferrous and nonferrous) pulp and paper Sensory and respiratory irritation, vegetation damage, corrosion, possible adverse effect on health... [Pg.2174]

Theoretical Oxygen and Air for Combustion The amount of oxidant (oxygen or air) just sufficient to burn the carbon, hydrogen, and sulfur in a fuel to carbon dioxide, water vapor, and sulfur dioxide is the theoretical or stoichiometric oxygen or air requirement. The chemical equation for complete combustion of a fuel is... [Pg.2379]

A substantial portion of fhe gas and vapors emitted to the atmosphere in appreciable quantity from anthropogenic sources tends to be relatively simple in chemical structure carbon dioxide, carbon monoxide, sulfur dioxide, and nitric oxide from combustion processes hydrogen sulfide, ammonia, hydrogen chloride, and hydrogen fluoride from industrial processes. The solvents and gasoline fractions that evaporate are alkanes, alkenes, and aromatics with relatively simple structures. In addition, more complex... [Pg.44]

TTte most cost-effective methods of reducing emissions of NO are the use of low-NO burners and the use of low nitrogen fuels such as natural gas. Natural gas has the added advantage of emitting almost no particulate matter or sulfur dioxide when used as fuel. Other cost-effective approaches to emissions control include combustion modifications. These can reduce NO emissions by up to 50% at reasonable cost. Flue gas treatment systems can achieve greater emissions reductions, but at a much higher cost. [Pg.28]

Today s major emissions control methods are sorbent injection and flue gas desulfurization. Sorbent injection involves adding an alkali compound to the coal combustion gases for reaction with the sulfur dioxide. Typical calcium sorbents include lime and variants of lime. Sodium-based compounds are also used. Sorbent injection processes remove 30 to 60% of sulfur oxide emissions. [Pg.41]

The Claus process consists of partial combustion of the hydrogen sulfide-rich gas stream (with one-third the stoichiometric quantity of air) and then reacting the resulting sulfur dioxide and unbumed hydrogen sulfide in the presence of a bauxite catalyst to produce elemental sulfur. Refer to the process flow diagram in Figure 7. [Pg.98]

Fire Hazards-Fto/iPomr (deg. F) 53 OC Flammable Limits in Air (%) No data Fire Extinguishing Agents Dry chemical, alcohol foam, carbon dioxide Fire Extinguishing Agents Not To Be Used Water Special Hazards of Combustion Products Irritating sulfur dioxide Behavior in Fire Vapors... [Pg.63]


See other pages where Sulfur dioxide combustion is mentioned: [Pg.262]    [Pg.509]    [Pg.262]    [Pg.509]    [Pg.18]    [Pg.389]    [Pg.485]    [Pg.453]    [Pg.54]    [Pg.172]    [Pg.3]    [Pg.8]    [Pg.301]    [Pg.145]    [Pg.151]    [Pg.183]    [Pg.31]    [Pg.259]    [Pg.483]    [Pg.1219]    [Pg.2173]    [Pg.2189]    [Pg.2371]    [Pg.37]    [Pg.17]    [Pg.29]    [Pg.65]    [Pg.138]    [Pg.273]   
See also in sourсe #XX -- [ Pg.78 ]

See also in sourсe #XX -- [ Pg.758 ]




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