Mercury hypochlorite

Dilute hydrochloric acid Lead (II) acetate or nitrate Cobalt nitrate Mercury Hypochlorites, OCh Yellow coloration, followed by chlorine gas evolution Brown lead (IV) oxide forms upon heating Black precipitate of cobalt (II) hydroxide On shaking slightly acidified solution of a hypochlorite with Hg, a brown precipitate of mercury (II) chloride is formed... 

Ammonia, anhydrous Mercury, halogens, hypochlorites, chlorites, chlorine(I) oxide, hydrofluoric acid (anhydrous), hydrogen peroxide, chromium(VI) oxide, nitrogen dioxide, chromyl(VI) chloride, sulflnyl chloride, magnesium perchlorate, peroxodisul-fates, phosphorus pentoxide, acetaldehyde, ethylene oxide, acrolein, gold(III) chloride... 

Oxalic acid Furfuryl alcohol, silver, mercury, sodium chlorate, sodium chlorite, sodium hypochlorite... 

Other recovery methods have been used (10). These include leaching ores and concentrates using sodium sulfide [1313-82-2] and sodium hydroxide [1310-73-2] and subsequentiy precipitating with aluminum [7429-90-3], or by electrolysis (11). In another process, the mercury in the ore is dissolved by a sodium hypochlorite [7681-52-9] solution, the mercury-laden solution is then passed through activated carbon [7440-44-0] to absorb the mercury, and the activated carbon heated to produce mercury metal. Mercury can be extracted from cinnabar by electrooxidation (12,13). 

When the mercury present in the atmosphere is primarily in the form of an organic mercury compound, it may be preferable to utilise an aqueous scmbber. This method is particularly useful for control of emissions from reactors and from dryers. For efficient and economical operation, an aqueous solution of caustic soda, sodium hypochlorite, or sodium sulfide is reckculated through the scmbber until the solution is saturated with the mercury compound. 

Mercury, chlorine, calcium hypochlorite, iodine, bromine or hydrogen fluoride Acids, metal powders, flammable liquids, chlorates, nitrites, sulphur, finely-divided organics or combustibles Nitric acid, hydrogen peroxide... 

Mercury, chlorine, calcium hypochlorite, iodine, bromine and hydrogen fluoride. 

MIcrobiocldes. There are several microbiocides available commercially that can perform an effective function in controlling microbial activity. Some of these chemicals are inorganic, such as chlorine, sodium hypochlorite, calcium hypochlorite, hydrogen peroxide, chromates and compounds of mercury and silver. However, the organic chemicals find the highest use as microbiocides. Some examples of these organic compounds are peracetic acid, paraformaldehyde, polychlorophenols and quaternary ammonium derivatives, to name a few [208]. 

Asbestos fibers, dissolved chlorine, dissolved hydrogen, sodium chloride lead, chlorinated organic compound Lead, chlorinated organic compound, such as methylene chloride and hexachlorinated benzenes Mercury, asbestos fibers, chlorinated hydrocarbons Hypochlorite... 

Acetone Acetylene Alkali and alkaline earth metals, e.g. sodium, potassium, lithium, magnesium, calcium, powdered aluminium Anhydrous ammonia Concentrated nitric and sulphuric acid mixtures Chlorine, bromine, copper, silver, flourine or mercury Carbon dioxide, carbon tetrachloride, or other chlorinated hydrocarbons. (Also prohibit, water, foam and dry chemical on fires involving these metals - dry sand should be available.) Mercury, chlorine, calcium hypochlorite, iodine, bromine or hydrogen fluoride... 

See Dinitrogen oxide or Halogens, both above Oxygen, below Calcium hypochlorite Acetylene Nitric acid Acetylene, Mercury(II) salts Nitrogen oxide Dienes, Oxygen Ozone Acetylene... 

Interaction of chlorine with methane is explosive at ambient temperature over yellow mercury oxide [1], and mixtures containing above 20 vol% of chlorine are explosive [2], Mixtures of acetylene and chlorine may explode on initiation by sunlight, other UV source, or high temperatures, sometimes very violently [3], Mixtures with ethylene explode on initiation by sunlight, etc., or over mercury, mercury oxide or silver oxide at ambient temperature, or over lead oxide at 100°C [1,4], Interaction with ethane over activated carbon at 350°C has caused explosions, but added carbon dioxide reduces the risk [5], Accidental introduction of gasoline into a cylinder of liquid chlorine caused a slow exothermic reaction which accelerated to detonation. This effect was verified [6], Injection of liquid chlorine into a naphtha-sodium hydroxide mixture (to generate hypochlorite in situ) caused a violent explosion. Several other incidents involving violent reactions of saturated hydrocarbons with chlorine were noted [7],... 

Nitropropane Nitrosyl fluoride Nitrosyl perchlorate Nitrourea Nitrous acid Nitryl chloride Oxalic acid See under Nitromethane chlorosulfonic acid, oleum Haloalkenes, metals, nonmetals Acetones, amines, diethyl ether, metal salts, organic materials Mercury(II) and silver salts Phosphine, phosphorus trichloride, silver nitrate, semicarbazone Ammonia, sulfur trioxide, tin(IV) bromide and iodide Furfuryl alcohol, silver, mercury, sodium chlorate, sodium chlorite, sodium hypochlorite... 

The existing mercury cell plant in Melbourne (ICI Mark 1 cells) is 14 000 tonnes per annum capacity whereas the market demand in Victoria, South Australia and Tasmania is 30 000 tonnes per annum. Owing to the age, condition and location of this plant (adjacent to residential areas and 5 km from the centre of Melbourne), it was decided to close this site and construct a new Greenfield plant in Laverton North, approximately 10 km away. The new plant includes chlor-alkali manufacture, sodium hypochlorite, hydrochloric acid, liquid chlorine storage and packing and chlor-paraffin manufacture. 

The Sydney plant is a combination of older mercury cell technology (updated ICI Mark 1 cells) and modern derivative plants (hydrochloric acid, sodium hypochlorite and ferric chloride) combined with liquid chlorine packing. The mercury cells had originally been in excess of 80 000 tonnes per annum capacity and cells had been progressively taken off-line following closure of chlorinated solvents (CTC/PCE) and EDC/VCM manufacture over a period of 10 years. This had left an asset significantly oversized compared with the present market demands. 

A. J. Balard found mercury immediately decomposes hypochlorous acid without the disengagement of any gas, but mercury oxychloride is formed. P. Grouvelle reported previously that when chlorine acts on mercuric oxide suspended in water, mercury oxychloride, very slightly soluble in cold water, is formed. L. J. Thenard found that the liquid contained both chloride and chlorate of mercury, also in soln. A. J. Balard, however, believed that these bodies are formed consecutively, and that their existence was preceded by that of a mercuric hypochlorite, as takes place with the salts of silver, and, as previously indicated, he prepared hypochlorous acid by the action of chlorine on mercuric oxide suspended in water. No mercury hypobromite has yet been isolated. There is a possible formation of mercury hypoiodite, or more probably of hypoiodous acid, when iodine is shaken up with... 

The orf/to-formylation of 2-aminopyridines can be effected via the rearrangement of the azasulfonium salt prepared from a 2-aminopyridine, 1,3-dithiane, f-butyl hypochlorite and sodium methoxide (74CC685). The crude sulfilimine (815) was refluxed in f-butanol containing potassium f-butoxide to yield the dithioacetal (816). Hydrolysis of (816) with mercury(II) oxide/boron trifluoride etherate gave the aldehyde (817 Scheme 191). This method should be applicable to the formylation of other heterocyclic amines. 

Caution. Chalcogenophenols have an unpleasant odor and are toxic. H2S, H2Se, or H2Te may be liberated on treatment with acid or exposure to the open air. These compounds should therefore be handled under inert gas in a well-ventilated hood. Contaminated glassware should be treated with sodium hypochlorite (bleach) solution for several hours and rinsed thoroughly with water and acetone before removal from the fume hood. Mercury and mercury salts are highly toxic, and skin and eye contact must be avoided. Mercury residues should be disposed of as toxic heavy metal waste. 

The A-chloro compound 176, obtained from the corresponding meth-oxyamide with f-butyl hypochlorite, was cyclized to l-methoxy-2-indolone 163 by silver carbonate in trifluoroacetic acid (87% yield) (84JA5728), or by other silver or mercury salts (87T2577), and more conveniently by anhydrous zinc acetate in 1,2-dichloroethane (91% yield) (87CL1771). The reaction proceeds through the spiro intermediate 177, followed by both possible 1,2-shifts. 

Mercury represents a serious environmental risk, and the study of removal of mercury from wastewater has received considerable attention in recent years. Mercury concentration was usually reduced by deposition on a cathode with high surface area. Removal of mercury is studied using extended surface electrolysis which reduces the level of mercury to below acceptable concentrations of 0.01 ppm in wastes by employing a Swiss roll cell with a cadmium-coated, stainless-steel cathode. An industrial cell with a fluidized bed electrode has also been studied. Graphite, as an efficient porous electrode, has been used to remove traces of mercuric ions form aqueous electrolyte solutions. In order to apply the electrochemical method for some effluents, it is necessary to use sodium hypochlorite to convert elemental mercury and less soluble mercury compounds to water-soluble mercuric-chloride complex ions. 

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