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25. colloidal ferric Precipitation, electrical

The colloid, as usually prepared, is electro-positive in character, and may be precipitated from solution by electrolysis, by the addition of small quantities of electrolytes, or by the action of an oppositely charged colloid, such, for example, as (negative) arsemous sulphide, whereby the two electrical charges neutralise each other.7 The smallest quantities of a few electrolytes required to precipitate colloidal ferric hydroxide from solution are given in the following table —8... [Pg.126]

A study of the electric conductivities of aqueous solutions of the salt indicates that the hydrolysis proceeds in two stages, embodying (1) a rapid change unaccompanied by precipitation, and (2) a slower change, progressing at a measurable rate, and accompanied by the production of a so-called basic salt.8 Colloidal ferric hydroxide does not appear to be formed during hydrolysis,9 the salt thus differing from ferric chloride and nitrate. [Pg.160]


See other pages where 25. colloidal ferric Precipitation, electrical is mentioned: [Pg.267]    [Pg.419]    [Pg.735]    [Pg.887]    [Pg.283]    [Pg.233]    [Pg.288]    [Pg.1179]    [Pg.270]   
See also in sourсe #XX -- [ Pg.247 ]




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25. colloidal ferric

Colloid precipitation

Electrical precipitation

Electrical precipitators

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