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Carbonyl sulfide hydrogen

Carbon dioxide, carbonyl sulfide, hydrogen cyanide, propylene, and butadiene... [Pg.268]

Dimethylbisthiomalonic acid (120), when treated with an acylated enol, produced intermediate 121 thietanediones 122 and 123 then were formed by elimination of thioketone and acetic acid (see Eq. 12). Similarly, cyclobutane-l,l-bisthiolcarboxylic acid gave 123, a previously unknown sulfur analog of malonic anhydride, (Eq. 12). Thermolysis of 120 also results in the formation of the four-membered heterocycles in addition to carbonyl sulfide, hydrogen sulfide, and thiocarbonic acid. ... [Pg.228]

Sulfur dioxide Carbonyl sulfide Hydrogen sulfide C1-C0 thiols... [Pg.37]

Boron trifluoride Carbonyl sulfide Hydrogen bromide... [Pg.262]

Carbonyl sulfide - hydrogen fluoride (1/1) Nearly linear... [Pg.152]

Ammonia, hydrogen sulfide, and carbon dioxide are major impurities in coke oven gas (COG). In addition to these three components, COG often contains caibon disulfide, carbonyl sulfide, hydrogen cyanide, organic acids, pyridine, phenol, and other impurities, which can cause problems with conventional amine plants. The presence of large quantities of ammonia in these gases naturally led to consideration of its use for removal of HjS and CO2, and several ammonia-based coke oven gas purification processes have been developed and commercialized. [Pg.281]

Oxygen Nitrogen Hydrogen Carbon monoxide Carbon dioxide Methane Hydrogen sulfide Sulfur dioxide Carbon (graphite) Diatomic sulfur Nitric oxide Carbonyl sulfide Hydrogen cyanide Ammonia Nitrous oxide... [Pg.116]

Sulfur might be present in inorganic forms elemental S, hydrogen sulfide H2S, carbonyl sulfide COS, or positioned within organic molecules as in the following ... [Pg.9]

Carbon disulfide [75-15-0] is a clear colorless liquid that boils at 46°C, and should ideally be free of hydrogen sulfide and carbonyl sulfide. The reaction with alkaU cellulose is carried out either in a few large cylindrical vessels known as wet chums, or in many smaller hexagonal vessels known as dry chums. In the fully continuous viscose process, a Continuous Belt Xanthator, first developed by Du Pont, is used (15). [Pg.347]

Conversion of carbon in the coal to gas is very high. With low rank coal, such as lignite and subbituminous coal, conversion may border on 100%, and for highly volatile A coals, it is on the order of 90—95%. Unconverted carbon appears mainly in the overhead material. Sulfur removal is faciUtated in the process because typically 90% of it appears in the gas as hydrogen sulfide, H2S, and 10% as carbonyl sulfide, COS carbon disulfide, CS2, and/or methyl thiol, CH SH, are not usually formed. [Pg.69]

In the reducing atmosphere of the reactor, sulfur compounds form hydrogen sulfide and small amounts of carbonyl sulfide [463-58-1J, COS, in a molar ratio of approximately 24 1. [Pg.422]

Petroleum Gases and Naphtha. Methane is the main hydrocarbon component of petroleum gases. Lesser amounts of ethane, propane, butane, isobutane, and some 0 + light hydrocarbons also exist. Other gases such as hydrogen, carbon dioxide, hydrogen sulfide, and carbonyl sulfide are also present. [Pg.167]

Alternative means for removal of carbonyl sulfide for gas streams iavolve hydrogenation. For example, the Beavon process for removal of sulfur compounds remaining ia Claus unit tail gases iavolves hydrolysis and hydrogenation over cobalt molybdate catalyst resulting ia the conversion of carbonyl sulfide, carbon disulfide, and other sulfur compounds to hydrogen sulfide (25). [Pg.130]

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]

When the Claus reaction is carried out in aqueous solution, the chemistry is complex and involves polythionic acid intermediates (105,211). A modification of the Claus process (by Shell) uses hydrogen or a mixture of hydrogen and carbon monoxide to reduce sulfur dioxide, carbonyl sulfide, carbon disulfide, and sulfur mixtures that occur in Claus process off-gases to hydrogen sulfide over a cobalt molybdate catalyst at ca 300°C (230). [Pg.144]

Carbon disulfide is essentially unreactive with water at room temperature, but above about 150°C in the vapor phase some reaction occurs forming carbonyl sulfide (carbon oxysulfide) [463-58-1] and hydrogen sulfide [7783-06-4]. Carbonyl sulfide is an intermediate in the hydrolysis reaction ... [Pg.27]

Charcoal—sulfur processes need low ash hardwood charcoal, prepared at 400—500°C under controlled conditions. At the carbon disulfide plant site, the charcoal is calcined before use to expel water and residual hydrogen and oxygen compounds. This precalcination step minimises the undesirable formation of hydrogen sulfide and carbonyl sulfide. Although wood charcoal is preferred, other sources of carbon can be used including coal (30,31), lignite chars (32,33), and coke (34). Sulfur specifications are also important low ash content is necessary to minimise fouling of the process equipment. [Pg.29]

The sulfur in the subbiturninous coal or lignite is converted mosdy to hydrogen sulfide. Small amounts of carbonyl sulfide are also produced. [Pg.270]

Although the continuous-countercurrent type of operation has found limited application in the removal of gaseous pollutants from process streams (Tor example, the removal of carbon dioxide and sulfur compounds such as hydrogen sulfide and carbonyl sulfide), by far the most common type of operation presently in use is the fixed-bed adsorber. The relatively high cost of continuously transporting solid particles as required in steady-state operations makes fixed-bed adsorption an attractive, economical alternative. If intermittent or batch operation is practical, a simple one-bed system, cycling alternately between the adsorption and regeneration phases, 1 suffice. [Pg.2187]

Natural gas - Determination of sulfur compounds. Determination of hydrogen sulfide, mercaptan sulfur, and carbonyl sulfide sulfur by potentiometry. Also BS 3156 Subsection 11.4.3 1994 Natural gas - Determination of sulfur compounds. Lmgener combustion method. Also BS 3156 Subsection 11.4.5 1994... [Pg.591]

The Beaven process is also effective in removing small amounts of sulfur dioxide, carbonyl sulfide, and carbon disulfide that are not affected by the Claus process. These compounds are first converted to hydrogen sulfide at elevated... [Pg.98]

Sulfur dioxide Sulfur dnoxide Hydrogen sulfide Carbon disulfide Carbonyl sulfide... [Pg.105]

Figure 14.3 Clnomatographic separation of sulfur compounds in propene, obtained by using the system illusti ated in Figure 14.2 1, hydrogen sulfide 2, carbonyl sulfide. Figure 14.3 Clnomatographic separation of sulfur compounds in propene, obtained by using the system illusti ated in Figure 14.2 1, hydrogen sulfide 2, carbonyl sulfide.
Sulfur Compounds. All crude oils contain sulfur in one of several forms including elemental sulfur, hydrogen sulfide, carbonyl sulfide (COS), and in aliphatic and aromatic compounds. The amount of sulfur-containing compounds increases progressively with an increase in the boiling point of the fraction. A majority of these compounds have one sulfur atom per molecule, but certain aromatic and polynuclear aromatic molecules found in low concentrations in crude oil contain two and even three sulfur atoms. Identification of the individual sulfur compounds in the heavy fractions poses a considerable challenge to the analytical chemist. [Pg.322]

Air, hydrogen sulfide, carbonyl sulfide, sulfur dioxide, methyl mercaptan, and carbon disulfide... [Pg.78]

Carbon dioxide, sulfur dioxide, carbonyl sulfide, acetylene, and hydrogen sulfide... [Pg.78]

Kremer L, Spicer LD. 1973. Gas chromatographic separation of hydrogen sulfide, carbonyl sulfide, and higher sulfur compounds with a single pass system. Anal Chem 45 1963-1964. [Pg.190]

Radford-Knoery J, Cutter GA. 1993. Determination of carbonyl sulfide and hydrogen sulfide species in natural waters using specialized collection procedures and gas chromatography with flame photometric detection. Anal Chem 65 976-982. [Pg.198]


See other pages where Carbonyl sulfide hydrogen is mentioned: [Pg.753]    [Pg.818]    [Pg.593]    [Pg.144]    [Pg.753]    [Pg.818]    [Pg.593]    [Pg.144]    [Pg.75]    [Pg.172]    [Pg.428]    [Pg.10]    [Pg.353]    [Pg.126]    [Pg.130]    [Pg.210]    [Pg.213]    [Pg.29]    [Pg.270]    [Pg.1541]    [Pg.201]    [Pg.140]    [Pg.347]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.5 , Pg.6 ]




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Carbonyl sulfide

Carbonyl sulfide hydrogenation

Hydrogen carbonylation

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