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Hydrogen chloride oxidation

Routes to chlorine from hydrogen chloride oxidation have been refined from the original commercial ventures of Weldon, which employed manganese dioxide (Eq. 8.54). The Weldon process permitted a maximum recovery of 50% of the chlorine in the hydrogen chloride consumed. Attempts to recycle the manganese (II) chloride met with mixed success [47]. [Pg.246]

The mechanism of the ethane oxidative chlorination process is distinguished by the fact that the catalyst accelerates primarily the reactions of hydrogen chloride oxidation and dichloroethane dehydrochlorination. This necessitates the modeling of cement catalytic system with the surface carrying active sites capable of catalyzing both reactions mentioned. [Pg.307]

Peroxyacetic acid/hydrogen chloride Oxidative isoxazolidine ring opening... [Pg.461]

Hydrogen peroxide/hydrogen chloride Oxidative ring contraction of isocyclics Benzene ring from tropenium salts... [Pg.476]

Hazardous Decomp. Prods. Under combustion hydrogen chloride, oxides of carbon and nitrogen, smoke, fumes HMIS Health 2, Flammability 1, Reactivity 0 Storage Keep container closed Hydropalat 44 [Cognis/Polymer, Coatings Inks]... [Pg.551]

Precaution Wear rubber or neoprene gloves, safety glasses Hazardous Decomp. Prods. CO, COj, hydrogen chloride, oxides of nitrogen Storage Store 40-120 F keep container closed avoid excessive heat Jeechem Shampoo Cone. 5 [Jeen Inti ]... [Pg.595]

By oxidation with permanganate it forms pinonic acid, C,oH,<503, a monobasic acid derived from cyclobutane. With strong sulphuric acid it forms a mixture of limonene, dipentene, terpinolene, terpinene, camphene and p-cymene. Hydrogen chloride reacts with turpentine oil to give CioHijCl, bomyl chloride, artificial camphor . [Pg.315]

Margottin-Maclou M, Doyennette L and Henry L 1971 Relaxation of vibrational energy in carbon monoxide, hydrogen chloride, carbon dioxide and nitrous oxide App/. Opt. 10 1768-80... [Pg.3015]

Arsenic forms a volatile trifluoride, ASF3, and a fairly volatile trichloride, ASCI3, which fumes in air. The latter is prepared by passing dry hydrogen chloride over arsenic(lll) oxide at 500 K ... [Pg.252]

In both reactions above, the oxide dichloride is refluxed with the acid or the hydrated chloride the sulphur dioxide and hydrogen chloride pass off and any unused sulphur oxide dichloride is distilled off in vacuo. [Pg.308]

By the oxidation of hydrogen chloride. A mixture of hydrogen chloride with air or oxygen is passed over a catalyst of copper(II)... [Pg.317]

Anhydrous hydrogen chloride is not particularly reactive, either as a gas at ordinary temperatures, or a liquid (b.p. 188 K) and does not react with metals such as iron or zinc, nor with dry oxides. A few reactive metals such as sodium, will bum in the gas to give the chloride and hydrogen ... [Pg.331]

However, if heated hydrogen chloride is passed over heated metals, the chloride is formed in the case of a metal exhibiting variable oxidation state, the lower chloride is obtained ... [Pg.331]

Thiazole acid chlorides react with diazomethane to give the diazoketone. The later reacts with alcoholic hydrogen chloride to give chloroacetylthiazole (Scheme 16). However, the Wolff rearrangement of the diazoketone is not consistently satisfactory (82). Heated with alcohol in the presence of copper oxide the 5-diazomethylketone (24) gives ethyl 5-thiazoleacetate (25) instead of the expected ethoxymethyl 5-thiazolyl ketone (Scheme 17) (83). [Pg.529]

Heavy water, see Hydrogen[ H] oxide Heazlewoodite, see rn-Nickel disulfide Hematite, see Iron(III) oxide Hermannite, see Manganese silicate Hessite, see Silver telluride Hieratite, see Potassium hexafluorosilicate Hydroazoic acid, see Hydrogen azide Hydrophilite, see Calcium chloride Hydrosulfite, see Sodium dithionate(III)... [Pg.274]

Moissanite, see Silicon carbide Molybdenite, see Molybdenum disulfide Molybdite, see Molybdenum(VI) oxide Molysite, see Iron(III) chloride Montroydite, see Mercury(II) oxide Morenosite, see Nickel sulfate 7-water Mosaic gold, see Tin disulfide Muriatic acid, see Hydrogen chloride, aqueous solutions... [Pg.274]

Bromoacetic acid can be prepared by the bromination of acetic acid in the presence of acetic anhydride and a trace of pyridine (55), by the HeU-VoUiard-Zelinsky bromination cataly2ed by phosphoms, and by direct bromination of acetic acid at high temperatures or with hydrogen chloride as catalyst. Other methods of preparation include treatment of chloroacetic acid with hydrobromic acid at elevated temperatures (56), oxidation of ethylene bromide with Aiming nitric acid, hydrolysis of dibromovinyl ether, and air oxidation of bromoacetylene in ethanol. [Pg.90]

Once the principal route to vinyl chloride, in all but a few percent of current U.S. capacity this has been replaced by dehydrochlorination of ethylene dichloride. A combined process in which hydrogen chloride cracked from ethylene dichloride was added to acetylene was advantageous but it is rarely used because processes to oxidize hydrogen chloride to chlorine with air or oxygen are cheaper (7) (see Vinyl polymers). [Pg.102]

The hydroxyl groups can be alkylated in the usual manner. Hydroxyalkyl ethers may be prepared with alkylene oxides and chloromethyl ethers by reaction with formaldehyde and hydrogen chloride (86). The terminal chlorides can be easily converted to additional ether groups. [Pg.106]

The U.S. domestic commercial potassium nitrate of the 1990s contains 13.9% N, 44.1% I+O, 0—1.8% Cl, 0.1% acid insoluble, and 0.08% moisture. The material is manufactured by Vicksburg Chemical Co. using a process developed by Southwest Potash Division of AMAX Corp. This process uses highly concentrated nitric acid to catalyze the oxidation of by-product nitrosyl chloride and hydrogen chloride to the mote valuable chlorine (68). The much simplified overall reaction is... [Pg.232]

Sulfur dioxide [7446-09-5] is formed as a result of sulfur oxidation, and hydrogen chloride is formed when chlorides from plastics compete with oxygen as an oxidant for hydrogen. Typically the sulfur is considered to react completely to form SO2, and the chlorine is treated as the preferred oxidant for hydrogen. In practice, however, significant fractions of sulfur do not oxidi2e completely, and at high temperatures some of the chlorine atoms may not form HCl. [Pg.58]


See other pages where Hydrogen chloride oxidation is mentioned: [Pg.299]    [Pg.527]    [Pg.951]    [Pg.645]    [Pg.165]    [Pg.980]    [Pg.1383]    [Pg.33]    [Pg.40]    [Pg.40]    [Pg.595]    [Pg.595]    [Pg.299]    [Pg.527]    [Pg.951]    [Pg.645]    [Pg.165]    [Pg.980]    [Pg.1383]    [Pg.33]    [Pg.40]    [Pg.40]    [Pg.595]    [Pg.595]    [Pg.305]    [Pg.19]    [Pg.210]    [Pg.259]    [Pg.3015]    [Pg.197]    [Pg.383]    [Pg.470]    [Pg.261]    [Pg.87]    [Pg.485]    [Pg.267]    [Pg.445]    [Pg.445]    [Pg.546]    [Pg.546]   
See also in sourсe #XX -- [ Pg.82 ]




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Hydrogen chloride, from oxidation

Hydrogen chloride, from oxidation chlorine compounds

Oxidation chloride

Oxidation of hydrogen chloride

Oxidation of hydrogen chloride by nitric acid

Oxide chlorides

Selenium oxides hydrogen chloride

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