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Chloramine Chloramines

For a long time, the Raschig process, which was discovered in 1907, was used for the production of hydrazine. Here, ammonia is oxidized with sodium hypochlorite in alkahne solution (pH = 8 11). In the initial rapid reaction, (55) sodium hypochlorite reacts with ammonia, forming chloramine. Chloramine then reacts with ammonia in a slower second reaction. ... [Pg.3040]

Effluents from sewage treatment plants can contain significant amounts of ammonia that when disinfected, instead of finding free chlorine, subsfilufion producfs of ammonia called chloramines are found. In addition, in water treatment plants, ammonia are often purposely added to chlorine. This, again, also forms the chloramines. Chloramines are disinfectants like chlorine, but they are slow reacting, and it is this slow-reacting property that is the reason why ammonia is used. The purpose is to provide residual disinfectant in the distribution system. In other words, the formation of chloramines assures that when the water arrives at the tap of the consumer, a certain amount of disinfectant still exists. [Pg.762]

In the commercial production of hydrazine by the Raschig process, a large excess of ammonium hydroxide and fresh sodium hypochlorite are first reacted to make chloramine. Chloramine is then converted to crude hydrazine by rapid heating. The reactor effluent, containing about 2.5 wt% of hydrazine, is stripped of unreacted ammonia. The hydrazine solution is then concentrated... [Pg.114]

N = 7,270 housing age, tap water sources, and change in water disinfection to using chloramines chloramines ... [Pg.390]

The primary use of anhydrous ammonia (ammonia gas) in water treatment is to combine with chlorine to form chloramines. Chloramines are used both as primary and secondary disinfectants. Use as a secondary disinfectant (residual in the distribution system) is more common. A typical treatment strategy is to use free chlorine to satisfy the USE PA regulatory CT requirements as a primary disinfectant. Ammonia is then added to combine with the free chlorine residual to form chloramines for use as the secondary distribution system disinfectant. The ammonia added is carefully controlled to ensure that all the free chlorine is combined and little free ammonia remains. This control is necessary because the presence of free chlorine can form regulated by-products. Free ammonia can increase the growth of nitrifying bacteria, thus causing residual demand that could lead to conditions that could violate the Total Coliform Rule. [Pg.29]

If ammonia is used in large excess and the chlorine diluted with nitrogen, chloramine, NH Cl, is formed ... [Pg.220]

When chlorine is passed into aqueous ammonia, ammonium chloride and nitrogen are formed. If, however, sodium chloratefi) (hypochlorite) is used instead of chlorine, chloramine is first formed ... [Pg.220]

Normally the chloramine immediately undergoes further reaction, giving oft nitrogen ... [Pg.220]

Toluene-p-sulphonchloro-sodio-amide ( Chloramine-T ), CHjC HjSO-NNaCh. H.O, and Toluene-p-sulphon-dichloro-amide ( Dickloramine-T ), CH3C H4S02Na2. [Pg.252]

Both chloramine-T and dichloramine-T have marked antiseptic properties, chloramine-T being most frequently used because of its solubility in water. Aqueous solutions of chloramine-T can be used either for external application, or for internal application to the mouth, throat, etc, as chloramine-T in moderate quantities is non-toxic its aqueous solution can also be effectively used when the skin has come in contact with many of the vesicant liquid poison-gases, as the latter are frequently organic sulphur or arsenic derivatives which combine with or are oxidised by chloramine-T and are thus rendered harmless. [Pg.253]

Both chloramine-T and dichloramine-T can be readily estimated, because they liberate iodine from potassium iodide quantitatively in the presence of... [Pg.253]

Dichloramine-T and chloramine-T. When p toluenesulphonamide is dissolved in excess of sodium (01 calcium) hypochlorite solution, it is converted into the soluble salt of the N-monochloro derivative ... [Pg.820]

When the dichloramine-T is heated with sodium hydroxide solution, the reverse change occurs and sodium N-chloro-p-toluenesulphoiiamide (chloramine-T) crystallises out on cooling at a suitable concentration ... [Pg.820]

Both chloramine-T and dichloramine-T slowly liberate hypochlorous aeid in eontaet with water and are therefore employed as antiseptics the former is employed in the form of a dilute (e.g., 0-2 per eent.) aqueous solution, and the latter (which is insoluble in water) as a solution in an organic solvent, such as a chlorinated paraffin. [Pg.821]

Chloramine-T is a salt and has no definite m.p. upon heating it loses water of crystallisation and decomposes violently at 175-180°. [Pg.824]

If the cut is Only a minor one, allow it to bleed for a few seconds, see that no glass remains, apply a disinfectant (rectified spirit, Dettol, 1 per cent aqueous chloramine-T solution, or sulpha-pyridine powder) and bandage. [Pg.1132]


See other pages where Chloramine Chloramines is mentioned: [Pg.102]    [Pg.81]    [Pg.87]    [Pg.102]    [Pg.81]    [Pg.87]    [Pg.91]    [Pg.91]    [Pg.199]    [Pg.401]    [Pg.220]    [Pg.224]    [Pg.252]    [Pg.253]    [Pg.253]    [Pg.325]    [Pg.820]    [Pg.823]    [Pg.824]    [Pg.220]    [Pg.395]    [Pg.41]    [Pg.81]    [Pg.131]    [Pg.193]    [Pg.193]    [Pg.193]    [Pg.193]    [Pg.193]    [Pg.193]    [Pg.193]   
See also in sourсe #XX -- [ Pg.98 , Pg.245 ]




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A-Chloramines

Acrylic acid Chloramine

Addition chloramines

Alkenes reaction with Chloramine

Amines, chloramination of tertiary boron halides

Amines, chloramination of tertiary coordination compounds with

Amino acids reactions with chloramines

Aminohydroxylation using chloramine

Ammonia chloramine species

Aqueous Chlorine (Chloramines)

Asymmetric aminohydroxylation chloramine

Boranes reaction with chloramine

Bromine-catalyzed Aziridination of Olefins with Chloramines

CT Values for Inactivation of Viruses by Chloramine

Cellulose Chloramine

Chemical techniques chloramine

Chloramide (chloramine

Chloramination

Chloramination

Chloramine

Chloramine

Chloramine amination

Chloramine amines

Chloramine as reactant

Chloramine compounds

Chloramine derivatives

Chloramine formation

Chloramine formation, hypochlorite

Chloramine hydrazines

Chloramine imidation with

Chloramine immobilized

Chloramine iodination protocol

Chloramine irradiation

Chloramine labelling with

Chloramine reaction with trialkylboranes

Chloramine reactions

Chloramine reactions with organoboranes

Chloramine secondary amines

Chloramine yellow

Chloramine, adsorption

Chloramine, coordinated

Chloramine, oxidation with

Chloramine, starch oxidized

Chloramine, with

Chloramine, with organoboranes

Chloramine-7 , estimation

Chloramine-B, oxidation

Chloramine-T , oxidation

Chloramine-T Protocol

Chloramine-T as Nitrene Precursor

Chloramine-T oxidant

Chloramine-T trihydrate

Chloramine-T,

Chloramine-T, as oxidant

Chloramine-T, radioiodination

Chloramine-T-Sodium iodide

Chloramines demand

Chloramines dichloramine

Chloramines monochloramine

Chloramines organic

Chloramines reactions with phenols

Chloramines reactivity

Chloramines sources

Chloramines taurine chloramine

Chloramines trichloramine

Chloramines, chlorine demand

Chloramines, nitration

Dichloramine-T and chloramine

Disinfection chloramine

F Carbonyl sulfide Chloramine

Formation and Reactions of Chloramines

Formation of Chloramines

Hydroboration with chloramine

Iodination chloramine

N-Chloramines

Oxidants examples: chloramine

Oxidation chloramines

Phenyl chloramine

Potable Water Chloramination Process Description

Potable water chloramination

Protein oxidation chloramine

Proteins chloramine

Radicals chloramines

Reactions with Halogens and Chloramines

Reactions with chloramine

Secondary disinfection chloramines

Selenium-Chloramine

Taurine chloramine

Taurine chloramine from

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