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In ammonia storage

Ammonia is corrosive to akoys of copper and zinc and these materials must not be used in ammonia service. Iron or steel should usuaky be the only metal in ammonia storage tanks, piping, and fittings. It is recommended that ammonia should contain at least 0.2% water to prevent steel stress corrosion. Mercury thermometers should be avoided. [Pg.354]

Some of the steps that can be taken to help minimize the impact of SCC in ammonia storage are Complete stress relief, operation without air contact and the addition of small amounts of water (0.2%) as an inhibitor. Low-temperature carbon steels have considerably more resistance to SCC than normal carbon steels. This makes them the preferred material of construction for large atmospheric liquid ammonia storage tanks that operate at -33°C88. [Pg.210]

Accidents in which fire and/or explosion of ammonia-air mixtures have been reported to cause the death or injury of personnel are known [77, 78], but are not very frequent. Such accidents have occurred in cold storage warehouses in which ammonia was released in an enclosed space and ignition was caused accidentally. One reason that explosions and lire accidents have not been frequent is that upon release of ammonia from atmospheric or pressurized tanks, rapid evaporation of ammonia cools down the liquid and thereby reduces the vapor pressure of ammonia over the liquid. As noted above, even momentary fatal concentrations of ammonia are much lower than the lower explosion limit in air. Also the fairly high ignition temperature and the low normal flame velocity of an ammonia/air mixture (0.07 to 0.08 m/s) are important [12]. For protection against fire and explosion in ammonia storage or transportation vessels see [13]. [Pg.332]

The reactor effluent, containing 1—2% hydrazine, ammonia, sodium chloride, and water, is preheated and sent to the ammonia recovery system, which consists of two columns. In the first column, ammonia goes overhead under pressure and recycles to the anhydrous ammonia storage tank. In the second column, some water and final traces of ammonia are removed overhead. The bottoms from this column, consisting of water, sodium chloride, and hydrazine, are sent to an evaporating crystallizer where sodium chloride (and the slight excess of sodium hydroxide) is removed from the system as a soHd. Vapors from the crystallizer flow to the hydrate column where water is removed overhead. The bottom stream from this column is close to the hydrazine—water azeotrope composition. Standard materials of constmction may be used for handling chlorine, caustic, and sodium hypochlorite. For all surfaces in contact with hydrazine, however, the preferred material of constmction is 304 L stainless steel. [Pg.282]

To reduce storage costs involved in such a cycHc consumption pattern, there has been substantial growth in the erection of large refrigerated anhydrous ammonia storage terminals at key points within large marketing areas. Terminal cost (84) is reported to add typically about 11.00/t. [Pg.356]

Determine whether a catastrophic failure of the ammonia storage tank could cause irreversible health impacts in a nearby neighborhood. [Pg.27]

Selective catalytic reduction (SCR) is cmrently the most developed and widely applied FGT technology. In the SCR process, ammonia is used as a reducing agent to convert NO, to nitrogen in the presence of a catalyst in a converter upstream of the air heater. The catalyst is usually a mixture of titanium dioxide, vanadium pentoxide, and hmgsten trioxide. SCR can remove 60-90% of NO, from flue gases. Unfortunately, the process is very expensive (US 40- 80/kilowatt), and the associated ammonia injection results in an ammonia slip stream in the exhaust. In addition, there are safety and environmental concerns associated with anhydrous ammonia storage. [Pg.28]

Particulate matter is the principal air pollutant emitted from ammonium sulfate plants. Most of the particulates are found in the gaseous exhaust of the dryers. Uncontrolled discharges of particulates may be of the order of 23 kg/t from rotary dryers and 109 kg/t from fluidized bed dryers. Ammonia storage tanks can release ammonia, and there may be fugitive losses of ammonia from process equipment. [Pg.65]

Gauges used for measuring the liquid level in vessels may be of semitransparent and even nontransparent materials. Figure 3.2 illustrates a simple level gauge on a steel vessel used for liquid ammonia storage. As shown, a narrow strip of insulation is taken away from the vessel s shell to expose the bare metal. Consequently, the heat transfer coefficient from the... [Pg.52]

If the possibility of reverse flow had been foreseen, then a slip-plate could have been inserted in the line leading to the ammonia storage vessel, as described in Section 1.1. [Pg.328]

A more serious incident occurred at a plant in which ethylene oxide and aqueous ammonia were reacted to produce ethanolamine. Some ammonia got back into the ethylene oxide storage tank, past several check valves in series and a positive pump. It got past the pump through the relief valve, which discharged into the pump suction line. The ammonia reacted with 30 m of ethylene oxide in the storage tank. There w as a violent rupture of the tank, followed by an explosion of the vapor cloud, which caused damage and destruction over a wide area [4],... [Pg.332]

The clear solution, obtained by centrifuging a solution of the oxide in aqueous ammonia which had been treated with silver nitrate until precipitation started, exploded on two occasions after 10-14 days storage in closed bottles in the dark. This was ascribed to slow precipitation of amorphous silver imide, which is very explosive even when wet [1], When silver oxide is dissolved in ammonia solution, an extremely explosive precipitate (probably Ag3N4) will separate. The explosive behaviour is completely inhibited by presence of colloids or ammonium salts (acetate, carbonate, citrate or oxalate). Substitution of methylamine for ammonia does not give explosive materials [2],... [Pg.22]

Silver solutions used in photography can become explosive under a variety of conditions. Ammoniacal silver nitrate solutions, on storage, heating or evaporation eventually deposit silver nitride ( fulminating silver ). Silver nitrate and ethanol may give silver fulminate, and in contact with azides or hydrazine, silver azide. These are all dangerously sensitive explosives and detonators [1], Addition of ammonia solution to silver containing solutions does not directly produce explosive precipitates, but these are formed at pH values above 12.9, produced by addition of alkali, or by dissolution of silver oxide in ammonia [2]. [Pg.385]

Ammonia is evaporated from animal manure in the stable, in the storage and during and after landspreading. The amount of ammonia lost from the manure depends on many factors as ... [Pg.32]

For some models adsorption or storage is important. For example, oxygen storage is important in a 3-way catalysis, a catalyst may contain a hydrocarbon storage component for improved low-temperature performance, and ammonia storage is important for ammonia SCR (selective catalytic reduction). Clearly, this sort of behaviour needs to be included in the final model. The nature of the measurements depends on the exact system being studied and will be discussed in more detail later. Suffice to say, from measurements at steady state, the heats of adsorption and coefficients of... [Pg.61]

According to the modified procedure (602), milk is thoroughly mixed in its storage container immediately before transfer of the 1 ml aliquot in the extraction tube. This is necessary because approximately 50% of phenylbutazone in milk is associated with the cream. The sample is extracted with 2.4 ml diethyl ether and 2.4 ml petroleum ether in presence of 1 ml ethanol and 100 1 25% ammonia solution. The organic layer that contains the milk lipids is discarded. Five ml hexane-tetrahydro furan (4 1) is added to the aqueous layer, which is tiien acidified with hydrochloric acid and the layers are mixed. Under the acidic conditions, phenylbutazone partitions quantitatively into tlie organic layer, which is collected, evaporated, and dissolved in the mobile phase to be analyzed by liquid chromatography. Separation is performed on a reversed-phase column using an isocratic 0.02 M phosphate buffer/methanol mobile phase, and determination is by ultraviolet detection at 264 nm (Fig. 29.18.2). The limit of detection and limit of quantification were 3.0 and 5.4 ppb, respectively (Table 29.17). [Pg.1123]

HS(G)30 Storage of anhydrous ammonia under pressure in the UK spherical and cylindrical vessels, HSE, 1986 (Not in current HSE list).Gives advice for the appropriate materials of construction for ammonia storage vessels. [Pg.53]


See other pages where In ammonia storage is mentioned: [Pg.36]    [Pg.80]    [Pg.226]    [Pg.228]    [Pg.65]    [Pg.196]    [Pg.36]    [Pg.80]    [Pg.226]    [Pg.228]    [Pg.65]    [Pg.196]    [Pg.355]    [Pg.36]    [Pg.1122]    [Pg.260]    [Pg.446]    [Pg.1176]    [Pg.654]    [Pg.276]    [Pg.276]    [Pg.6]    [Pg.301]    [Pg.261]    [Pg.126]    [Pg.164]    [Pg.348]    [Pg.836]    [Pg.180]    [Pg.348]    [Pg.464]    [Pg.1116]   
See also in sourсe #XX -- [ Pg.127 ]




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Ammonia storage

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