Abstract: A process is provided for the production of hydrogen from hydrogen sulfide by reacting carbon monoxide with hydrogen sulfide to produce hydrogen and carbonyl sulfide, and then reacting the carbonyl sulfide with oxygen to produce carbon monoxide and sulfur dioxide. The carbon monoxide is recycled back to the hydrogen sulfide reaction step. The catalyst used to promote the reaction between carbonyl sulfide and oxygen is an oxide of a metal, such as V, Nb, Mo, Cr, Re, Ti, W, Mn or Ta, which is supported on a support, such as TiO2, ZrO2, CeO2, Nb2O5 and Al2O3.

Abstract: A method of preparing sulfuryl fluoride by disproportionation of sulfuryl chloride fluoride in the gas phase on activated carbon.

Abstract: This invention relates to a process for generating recoverable sulfur containing compounds, e.g., sulfur dioxide, from a spent sulfuric acid stream by combusting and/or thermally decomposing the spent sulfuric acid stream in a furnace. The spent sulfuric acid stream is sprayed into the furnace through a spray nozzle designed to minimize the spent sulfuric acid droplet size, e.g., to produce droplets having a Sauter mean diameter of from 200 micrometers to 700 micrometers.

Abstract: Nascent hydrogen and nascent oxygen are used to convert calcium sulfate and silicon dioxide to calcium silicate and sulfur dioxide.

Abstract: A flue gas conditioning system (FGC) for conditioning the flue gas flowing in a flue from a boiler to an electrostatic precipitator by injecting sulfur trioxide into the flue gas upstream of the electrostatic precipitator. The FGC has a source (52) of granulated sulfur which is transported by a conveyor (54) to a sulfur furnace (60) where it is combusted in sulfur dioxide. The sulfur dioxide flows from the sulfur furnace (60) into a catalytic converter 62 which generates sulfur trioxide therefrom. The sulfur trioxide flows from the catalytic converter 62 into probes 64 which are mounted in the flue duct. Alternatively, the FGC has a source (70) of emulsoid sulfur which is pumped by a sulfur pump (72) to the inlet of an atomizing spray nozzle (200) which atomizes the emulsoid sulfur and sprays it into sulfur furnace (50).

Abstract: A process is disclosed for treating an exhaust gas stream containing COS and CO arising from chlorinating titanium-containing material with a cold plasma wherein oxygen is present and selectively oxidizing COS.

Abstract: After hydrogenation and desulfurization treatment of raw fuel in the desulfurization unit 1, the product is separated in the acidic gas separator 2 into fuel and a hydrogen sulfide-containing gas, and the hydrogen sulfide-containing gas is subjected to combustion together with air in the catalyst converter 3 thereby converting the hydrogen sulfide completely into sulfur dioxide to give a sulfur dioxide-containing gas, and this sulfur dioxide-containing gas is reacted with limestone powder and air in water in the oxidation and neutralization reactor 4, and the resulting slurry is dehydrated in the gypsum slurry solid/liquid separator 5 and then dried in the gypsum heater 6.

Abstract: An improved method and system for cooling the sulfur dioxide gas stream flowing from a sulfur furnace to a catalytic converter in a sulfur trioxide flue gas conditioning system. Water is injected into the sulfur dioxide gas stream upstream of the catalytic converter as appropriate to maintain the temperature at the inlet of the catalytic converter at a desired level.

Abstract: An apparatus and process for removing and incinerating sulfur from tail gas being emitted from a Claus Recovery Sulfur Unit (SRU) or a Tail Gas Clean-up Unit (TGCU) is provided. The gas is processed in a Z-Sorb.TM. type sulfur absorber wherein the off-gas, after the hydrogen sulfide is removed, is combusted and used as a regenerative gas for a second absorber, that has been used to sorb hydrogen sulfide out of a gas, so as to release sulfur dioxide from the second absorber--in lieu of "process to substantially convert the hydrogen sulfide to sulfur dioxide, toward precluding the need for combustion of the hydrogen sulfide.

Abstract: The present invention is directed to methods for preparing sulfur hexafluoride by reacting sulfur tetrafluoride with oxygen. The sulfur tetrafluoride is prepared by contacting molten sulfur with a metal fluoride to produce sulfur tetrafluoride and a metal sulfide. In a preferred method, the metal fluoride is regenerated from the metal sulfide by reacting the metal sulfide with hydrofluoric acid in the presence of oxygen. The preferred metal fluorides are the fluorides of copper, silver, mercury and mixtures thereof.

Abstract: There is provided a process for the catalytic production of hydrogen from the reaction of hydrogen sulfide and carbon monoxide with the elimination of the carbonyl sulfide and/or sulfur dioxide by-products. The carbonyl sulfide and the sulfur dioxide are combusted or reacted in one or more reaction steps with each other, oxygen and/or hydrogen sulfide to produce carbon dioxide, water, sulfur or sulfuric acid or a combination of these.

Abstract: A method of treating a flow of gas containing oxidized sulphur compounds, such as an exhaust gas from coal combustion, comprising the steps of (i) treating the flow of gas to obtain a first component flow containing at least 30% of the total oxidized sulphur compounds and a second component flow containing at least a part of the remainder of the total oxidized sulphur compounds; (ii) converting the first component flow into a concentrated gas containing at least 2.5% by volume of sulphur compounds; (iii) converting oxidized sulphur compounds in the second component flow into hydrogen sulphide; and (iv) supplying the concentrated gas of step (ii) and the hydrogen sulphide of step (iii) to an apparatus for manufacturing either sulfuric acid, sulphur dioxide or elemental sulphur.

Abstract: A method for reducing contaminant concentrations in a fluid stream including the steps of forming a metal-complexed material having a surface suitable for exchange with the contaminant, contacting the fluid stream with the metal-complexed material, immobilizing at least a portion of the contaminant on the surface of the metal-complexed material, and regenerating the metal-complexed material so as to remove the contaminant from the surface of the metal-complexed material. The metal-complexed material is formed by the encapsulating of a core of ferromagnetic material with an ion exchange material. The metal-complexed material is magnetically affixed to a metallic mesh retaining surface.

Abstract: A multi-bed process of removing sulfur oxides and/or other combustible sulfur-containing compounds from a gas stream including combusting the other combustible sulfur-compounds when present in the gas stream with air or oxygen to convert such sulfur-containing compounds to sulfur oxide and form a sulfur oxide enriched gas stream. The sulfur oxide enriched gas stream is contacted with first and second serially connected solid adsorbent beds for adsorbing the sulfur oxides in the form of inorganic sulfates and/or sulfur oxides. A third adsorbent bed is contacted with a reducing gas stream to regenerate the bed by reducing the retained inorganic sulfates and/or sulfur oxides to hydrogen sulfide and/or sulfur dioxide, to thereby form a hydrogen sulfide and/or sulfur dioxide bearing stream. The feeds to each of the beds are realigned to place the second and third beds in series with the sulfur oxide and/or sulfur dioxide enriched stream being fed to the second bed and to place the first bed in a regenerative mode.

Abstract: A chemisorption reaction process is carried out under conditions in which the volumetric expansion of the complex compound reaction product is restricted, and at half-cycle reaction periods of less than 30 minutes each, and/or in a reaction chamber having a maximum mean mass diffusion path length of less than about 15 mm, and/or a maximum heat diffusion path length of less than 1.5 mm.

Abstract: Sulphur dioxide is separated from the flue gases of a cellulose pulp mill by absorbing it into a sodium sulphite solution. Sulphur dioxide is regenerated from the sodium bisulphite solution produced by an evaporation-crystallization method utilizing thermo-compressor evaporation technique. A lamella evaporator is utilized as the evaporator-crystallizer, the evaporator being divided into separate compartments for ease of cleaning the lamella surfaces. The recovered concentrated sulphur dioxide can be used wherever desired, for example for the production of chlorine dioxide.

Abstract: Sulfur compounds poison catalysts, such as the anode catalysts and reformer catalysts within molten carbonate fuel cell systems. This poisoning is eliminated using a sulfur scrubber 29 located prior to the inlet of the cathode chamber 13. Anode exhaust 19 which contains water, carbon dioxide and possibly sulfur impurities, is combined with a cathode exhaust recycle stream 22 and an oxidant stream 25 and burned in a burner 33 to produce water, carbon dioxide. If sulfur compounds are present in either the anode exhaust, cathode exhaust stream, or oxidant stream, sulfur trioxide and sulfur dioxide are produced. The combined oxidant-combustion stream 27 from the burner 33 is then directed through a sulfur scrubber 29 prior to entering the cathode chamber 13. The sulfur scrubber 29 absorbs sulfur compounds from the combined oxidant-combustion stream 27. Removal of the sulfur compounds at this point prevents concentration of the sulfur in the molten carbonate fuel cell system.

Abstract: Reaction rates in chemisorption reactions involving solid reactants and gaseous ligands are improved by maintaining optimized solid density throughout the reaction. Methods and apparatus which restrict volumetric solid expansion, compression of the solid reactant, and mixture with inert solid porous or particulate materials are disclosed.

Abstract: Sodium (bi)sulfites are produced by the steps of:(a) introducing a stream of aqueous sodium carbonate into the top end of a main packed column reactor;(b) introducing a stream of sulfur dioxide gas into the top end of the main packed column reactor concurrently with the stream of aqueous sodium carbonate;(c) allowing the aqueous sodium carbonate and sulfur dioxide to cocurrently flow downward from the top end of the main packed column reactor to the bottom of the column in a cocurrent flow, during which flow reaction occurs between the aqueous sodium carbonate and the sulfur dioxide to produce sodium (bi)sulfite; and(d) recovering the product sodium (bi)sulfite and a gas stream containing any excess sulfur dioxide from the bottom of the main packed column reactor. The product (bi)sulfite can be separated from the gas stream in a separate receiving vessel and then the gas is sent to a scrubber to remove residual SO.sub.2. The scrubber may be a second packed column reactor operating with cocurrent flow.

Abstract: A process for the separation of elemental sulfur from a gas comprises contacting the gas with molten sulfur whereby to extract the sulfur from the gas.

Abstract: A method of making high purity sulfur dioxide by submerged combustion is disclosed. Sulfur is combusted in a first liquid pool with an oxygen-containing gas and the vapor effluent is removed and cooled in a first cooling zone to a temperature above approximately 600.degree. F. The condensed sulfur is separated as liquid sulfur from the vapor in the cooled effluent and passed back to the reactor as the supply of liquid sulfur for conversion to sulfur dioxide.

Abstract: Solid catalyst substrates based on zirconium dioxide and, optionally, titanium dioxide and/or cerium dioxide, e.g., honeycombs or monoliths, are well adapted for the desulfurization and catalytic conversion of industrial gases containing contaminating amounts of objectionable sulfur compounds.

Abstract: A method for production of sulfur dioxide from calcium sulfate by high temperature thermal reduction. Calcium sulfate, preferably in the form of calcined phosphogypsum, is desulfurized using a fossil fuel as a heat source, the combustion products resulting therefrom being used as a reductant. The fuel and reductant may be coal, coke, liquid hydrocarbons or natural gas; high sulfur, medium or low rank coal is preferred. The fuel is combusted with air or oxygen-enriched air. The solid feeds are introduced as finely-divided particles entrained in reactant gases, and the temperature is sufficiently hot to cause residual processed materials to melt and drain from the reaction vessel in the form of a liquid slag, yet not hot enough to produce significant amounts of fine silicon oxide dust. Iron pyrite, sand and/or clay can be added to reduce the slag melting point and to control its viscosity.

Abstract: A counter-current contacting device which includes a number of features which increase the efficiency and/or increase the pressure differential across the device is disclosed. Systems for reducing the alcohol content of an alcohol containing beverage or wine, for stripping aroma and flavor from a fruit juice and for desulphuring a liquid containing dissolved sulphur dioxide are also disclosed. Each of these systems incorporate a counter-current contact device of the invention.

Abstract: An improved apparatus for burning sulfur to sulfur dioxide and generating sulfurous acid comprising a primary sulfur-burning chamber, a sulfur feed tank closely coupled to the primary chamber, a secondary sulfur burning chamber, and an absorption tower, Air is drawn into the primary chamber under turbulent, high velocity negative pressure conditions. Gas passes through the secondary chamber under turbulent negative pressure flow conditions. The apparatus is capable of converting sulfur to sulfur dioxide at a rate in excess of 25 pounds of sulfur per hour per square foot of surface area of the molten pool of sulfur in the primary chamber.

Abstract: A pelletized mixture of gypsum, carbonaceous material and pyrite is charged to a travelling grate where the charge is heated under suitable conditions to produce a solid sintered material which has a broad spectrum of applications due to its chemical and physical properties and a gaseous effluent containing sulfur dioxide, sulfur or mixtures thereof.

Abstract: The present invention provides a process for recovering boron trifluoride from an impure gaseous boron trifluoride residue. The process comprises: (a) feeding an impure gaseous boron trifluoride residue containing sulfur dioxide as an impurity into a mixture of boric and sulfuric acids wherein the acid mixture absorbs boron trifluoride from the impure boron trifluoride residue and slightly absorbs or does not absorb sulfur dioxide from the impure gaseous boron trifluoride residue; and (b) removing the unabsorbed sulfur dioxide from the acid mixture.The present invention also provides a boron trifluoride preparation and purification process.

Abstract: A process for the preparation of sulphur dioxide by the thermal decomposition of metal sulphates in a fluidized bed reactor with sulphur-containing reducing agents and energy suppliers, characterized in that a mixture comprising the metal sulphates, the sulphur-containing reducing agents and 75 to 99% of the energy suppliers is fed into the fluidized bed reactors and the remainder of the energy suppliers is introduced separately into the fluidized layer of the fluidized bed reactor.

Abstract: The present invention is related to a method for preventing the formation of NH.sub.4 HSO.sub.4 during the noncatalytic reduction of nitric oxide by ammonia or ammonia precursors in combustion effluents. The formation of this sticky and corrosive substance inside combustion units is an extreme limitation upon the usefulness of nitric oxide reduction processes, particularly in boilers, furnaces, and other combustion devices.The present invention specifically teaches the use of methanol to reduce SO.sub.3 in the effluent stream to SO.sub.2. The noncatalytic reduction of SO.sub.3 by methanol is selective in that a large fraction of the SO.sub.3 is converted to SO.sub.2, while on a percentage basis very little oxygen is consumed. In addition, the process of the present invention allows the amount of methanol to be limited such that significant amounts of carbon monoxide are not produced and emitted with the effluent stream.

Abstract: A process for removing sulfur dioxide from flue gas is disclosed. After passing through a precipitator to remove particulate material, the flue gas is conducted continuously through a fixed bed solid-gas contacting device containing activated carbon or natural zeolite. The bed is regenerated continuously, thereby producing sulfuric acid which may be mixed with ground phosphate rock to produce normal superphosphate, or other by-products.

Abstract: A process of abstracting sulfur from H.sub.2 S and generating hydrogen is disclosed comprising dissolving Pd.sub.2 X.sub.2 (.mu.-dppm).sub.2 in a solvent and then introducing H.sub.2 S. The palladium complex abstracts sulfur, forming hydrogen and a (.mu.-S) complex. The (.mu.-S) complex is readily oxidizable to a (.mu.-SO.sub.2) adduct which spontaneously loses SO.sub.2 and regenerates the palladium complex.

Abstract: Process and apparatus for the generation of sulphur dioxide vapor from contaminated liquid sulphur dioxide. The process allows of utilization of contaminated liquid sulphur dioxide and comprises subjecting liquid sulphur dioxide feed to microwave energy for a sufficient period of time to produce sulphur dioxide vapor, collecting said vapor and removing resultant contaminated liquid sulphur dioxide, if any.

Abstract: A process for purifying sulfuric dioxide gas prepared by the combustion of sulfur containing compounds by scrubbing the gas with a sulfuric and composition having a sulfuric acid content of at least about 85 percent by weight based on the total weight of the composition.

Abstract: Process for the production of liquid sulphur dioxide in a sulphur dioxide facility forming part of a sulphuric acid plant wherein a portion of the sulphur dioxide produced in a sulphur burning furnace is directed to a sulphur dioxide liquefaction means and the resultant tail gas is recycled to the furnace. Relatively high sulphur dioxide concentrations are maintained in all parts of the sulphur dioxide production cycle allowing higher strength sulphur dioxide gases to be generated without overheating the furnace and also lower power requirements in the sulphur dioxide liquefaction step.

Abstract: Catalysts comprising bismuth and vanadium components are highly active and stable, especially in the presence of water vapor, for oxidizing hydrogen sulfide to sulfur or SO.sub.2. Such catalysts have been found to be especially active for the conversion of hydrogen sulfide to sulfur by reaction with oxygen or SO.sub.2.

Abstract: Sulfur species are removed from a Claus plant tail gas stream by contacting with zinc oxide in the presence of sufficient reducing equivalents for conversion of sulfur compounds to hydrogen sulfide. In another aspect, sulfur compounds are converted to hydrogen sulfide prior to contacting with zinc oxide.

Abstract: A highly efficient apparatus for burning sulfur to sulfur dioxide and generating sulfurous acid comprises a primary sulfur-burning chamber, a sulfur feed tank closely coupled to the primary chamber, a secondary sulfur-burning chamber, and an absorption tower. Air is introduced to the primary chamber under turbulent, high-velocity flow conditions. Gas passes through the secondary chamber under turbulent flow conditions. The apparatus is capable of converting sulfur to sulfur dioxide at a rate in excess of 25 pounds of sulfur per hour per square foot of surface area of the molten pool of sulfur in the primary chamber.

Abstract: A process is provided for the recovery of sulfur dioxide liberated in the chemical pulping of lignocellulosic material, which comprises(1) collecting sulfur dioxide-containing gas emitted during the pulping and separating it into at least two portions;(2) contacting at least one portion with chlorine gas, thereby forming a gaseous mixture comprising sulfur dioxide and chlorine;(3) effecting reaction of sulfur dioxide, chlorine and water to form hydrochloric acid and sulfuric acid while forming an intimate dispersion in said gaseous mixture of an aqueous solution of hydrochloric acid and sulfuric acid;(4) dissolving said hydrochloric acid and sulfuric acid in said solution;(5) recovering said solution and separating it from substantially sulfur dioxide-free residual gas.

Abstract: A system for desulfurization of sulfur-containing coal comprises apparatus for comminuting sulfur-containing coal, a gas/solid reactor having an inlet and an outlet, a connection or conduit for supplying the comminuted sulfur-containing coal to the reactor inlet, and an oxidant gas generator constructed in accordance with U.S. Pat. No. 4,248,681 connected to supply an oxidant gas to the reactor. The oxidant gas produced from concentrated salt solutions contains substantial amounts of chlorine dioxide, while the oxidant gas produced from dilute salt solutions contains other oxygen-containing gases. The oxidant gas is introduced at pressures which may range from sub-atmospheric to super-atomospheric and the comminuted coal is mixed or agitated to insure efficient gas/solid contact. The oxidant gas oxidizes the sulfur contaminants of the coal to gaseous sulfur oxides which are removed from the reactor. The desulfurized comminuted coal may be slurried for pipeline transmission.

Abstract: Sulfur dioxide is prepared by reacting sulfur with sulfur trioxide in a medium which is sulfuric acid containing 10-65% by weight of sulfur trioxide, and which is held at a temperature of 100-150.degree. C.

Abstract: A process to remove SO.sub.2 from mixtures by contacting SO.sub.2 -containing mixtures with a regenerable iron-bearing sorbent such as paint rock under reaction conditions to produce iron sulfide and an effluent containing reduced amounts of SO.sub.2.

Abstract: A process for preparing a gas stream containing sulfur dioxide and water for reaction with coal to convert the sulfur dioxide to gaseous elemental sulfur. Water is initially removed from the gas stream to increase the percentage of sulfur dioxide in the stream after which the gas stream is passed through the flame of a burner to add combustion gases to the gas stream. Steam is then mixed with the gas stream to increase the percentage of water in the gas stream before it is reacted with the coal.

Abstract: A process and apparatus for continuous copper smelting, slag conversion, and production of blister copper in the same furnace by enriched oxygen containing gas injection.

Abstract: Hydrogen is recovered from aqueous hydriodic acid in the presence of sulfuric acid, in an electrolysis cell having an anode and cathode compartment separated by a hydrogen ion permeable membrane, by electrochemically liberating iodine in the anode compartment by anodization of iodide anions, and electrochemically generating hydrogen in the cathode compartment from hydrogen cations that migrate across the membrane.

Abstract: There are disclosed manganese compounds of the formulaMn.sup.II LX.sub.2 (Q).sub.n (I)wherein L is a monodentate ligand of the formulaPR.sup.1 R.sup.2 R.sup.3 (II)whereinR.sup.1, R.sup.2, and R.sup.3 are identical or different and are substituted or unsubstituted alkyl, cycloalkyl, alkenyl, alkynyl, or aryl or hydrogen providing that no more than two of the R.sup.1, R.sup.2, and R.sup.3 groups are substituted or unsubstituted aryl groups and that at least one of R.sup.1, R.sup.2 and R.sup.3 is a substituted or unsubstituted alkyl, cycloalkyl, alkenyl, alkynyl, or aryl group,X is a species capable of existing as an anion, e.g., Cl, Br,Q is a solvento molecule capable of forming a chemical bond to the manganese, andn is 1, 2, or 3 solvent donor atoms.The manganese compounds are useful in the separation of a gas such as oxygen, hydrogen, sulfur dioxide, an alkene, and carbon monoxide from fluids containing these gases.

Abstract: Catalysts comprising bismuth and vanadium components are highly active and stable, especially in the presence of water vapor, for oxidizing hydrogen sulfide to sulfur or SO.sub.2. Such catalysts have been found to be especially active for the conversion of hydrogen sulfide to sulfur by reaction with oxygen or SO.sub.2.

Abstract: Catalysts comprising bismuth and vanadium components are highly active and stable, especially in the presence of water vapor, for oxidizing hydrogen sulfide to sulfur or SO.sub.2. Such catalysts have been found to be especially active for the conversion of hydrogen sulfide to sulfur by reaction with oxygen or SO.sub.2.

Abstract: Catalysts comprising bismuth and vanadium components are highly active and stable, especially in the presence of water vapor, for oxidizing hydrogen sulfide to sulfur or SO.sub.2. Such catalysts have been found to be especially active for the conversion of hydrogen sulfide to sulfur by reaction with oxygen or SO.sub.2.

Abstract: Mixing of carbon in the form of high sulfur coal with sulfuric acid reduces the temperature of sulfuric acid decomposition from 830.degree. C. to between 300.degree. C. and 400.degree. C. The low temperature sulfuric acid decomposition is particularly useful in thermal chemical cycles for splitting water to produce hydrogen. Carbon dioxide is produced as a commercially desirable byproduct. Lowering of the temperature for the sulfuric acid decomposition or oxygen release step simplifies equipment requirements, lowers thermal energy input and reduces corrosion problems presented by sulfuric acid at conventional cracking temperatures. Use of high sulfur coal as the source of carbon for the sulfuric acid decomposition provides an environmentally safe and energy efficient utilization of this normally polluting fuel.

Abstract: Catalysts comprising bismuth and vanadium components are highly active and stable, especially in the presence of water vapor, for oxidizing hydrogen sulfide to sulfur or SO.sub.2. Such catalysts have been found to be especially active for the conversion of hydrogen sulfide to sulfur by reaction with oxygen or SO.sub.2.