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Coal with hydrogen peroxide, oxidation

Coal (72 mesh) slurried with hydrogen peroxide solution (30 wt%) reacts steadily on warming to 85°C, but if much pyrites is present, the oxidation may accelerate to a dangerous extent. [Pg.1632]

CO is derived from a variety of feedstocks such as petroleum gas, fuel oil, coal, and biomass. The industrial scale production of PO starts from propylene, which is mainly obtained from crude oil. However, due to the high importance of this compound, many pathways from renewable sources have additionally been developed [54]. PP is converted to PO by either hydrochlorination or oxidation [55]. The use of chlorine leads to large amounts of salts as by-products, therefore oxidation methods are more important, such as the co-oxidation of PP using ethylbenzene or isobutene in the presence of air and a catalyst. However, this process is economically dependent on the market share of these by-products, thus new procedures without significant amounts of other side-products have been developed, such as the HPPO (hydrogen peroxide to propylene oxide) process in which propylene is oxidized with hydrogen peroxide to give PO and water [56, 57] (Fig. 14). [Pg.64]

The hexamine cobalt (II) complex is used as a coordinative catalyst, which can coordinate NO to form a nitrosyl ammine cobalt complex, and O2 to form a u -peroxo binuclear bridge complex with an oxidability equal to hydrogen peroxide, thus catalyze oxidation of NO by O2 in ammoniac aqueous solution. Experimental results under typical coal combusted flue gas treatment conditions on a laboratory packed absorber- regenerator setup show a NO removal of more than 85% can be maitained constant. [Pg.229]

Sulfurous acid. Sulfur dioxide (SO2) from the burning of high-sulfur coal forms sulfurous acid in contact with water. Oxidizing air pollutants, such as hydrogen peroxide, convert sulfurous acid to sulfuric acid ... [Pg.639]

A high-temperature combustion method for the determination of sulfur in solid fuels has also been adopted in many laboratories and is advantageous insofar as chlorine can be determined simultaneously. The method requires that the coal sample be heated to 1250°C-1350°C (2280 F-2460°F) in the presence of excess kaolin, ferric phosphate, or aluminum oxide to enhance the ranoval of the sulfur (as sulfate) from the ash. Oxygen is also included to produce oxides of sulfur which are absorbed in hydrogen peroxide (whereby sulfur dioxide is converted to sulfur trioxide). The solution is then titrated with standard alkali solution which gives the total acidity (due to the hydrochloric and sulfuric acids that are formed). [Pg.234]


See other pages where Coal with hydrogen peroxide, oxidation is mentioned: [Pg.196]    [Pg.1254]    [Pg.367]    [Pg.765]    [Pg.170]    [Pg.302]    [Pg.68]    [Pg.232]    [Pg.1001]    [Pg.201]    [Pg.251]    [Pg.4]    [Pg.1693]    [Pg.585]    [Pg.170]    [Pg.7]    [Pg.110]    [Pg.1687]    [Pg.674]    [Pg.26]    [Pg.1100]    [Pg.429]    [Pg.130]    [Pg.642]    [Pg.377]   
See also in sourсe #XX -- [ Pg.251 ]




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Coal oxidation

Coal oxidized

Coals hydrogenation

Hydrogenating coal

Oxidants peroxides

Oxidation hydrogen peroxide

Oxidation peroxidation

Oxidation with hydrogen

Oxidation with peroxides

Oxides peroxides

Oxidizers hydrogen peroxide

Peroxidative oxidation

Peroxidative oxidation hydrogen peroxide)

Peroxides oxidation

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