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Hydroxides, precipitation

Another important parameter that may affect a precipitate s solubility is the pH of the solution in which the precipitate forms. For example, hydroxide precipitates, such as Fe(OH)3, are more soluble at lower pH levels at which the concentration of OH is small. The effect of pH on solubility is not limited to hydroxide precipitates, but also affects precipitates containing basic or acidic ions. The solubility of Ca3(P04)2 is pH-dependent because phosphate is a weak base. The following four reactions, therefore, govern the solubility of Ca3(P04)2. [Pg.237]

A fourth mechanism is called sweep flocculation. It is used primarily in very low soflds systems such as raw water clarification. Addition of an inorganic salt produces a metal hydroxide precipitate which entrains fine particles of other suspended soflds as it settles. A variation of this mechanism is sometimes employed for suspensions that do not respond to polymeric flocculants. A soHd material such as clay is deUberately added to the suspension and then flocculated with a high molecular weight polymer. The original suspended matter is entrained in the clay floes formed by the bridging mechanism and is removed with the clay. [Pg.34]

In aqueous solutions, trivalent lanthanides ate very stable whereas only a limited number of lanthanides exhibit a stable divalent or tetravalent state. Practically, only Ce and Eu " exist in aqueous solutions. The properties of these cations ate very different from the properties of the trivalent lanthanides. For example, Ce" " is mote acidic and cetium(IV) hydroxide precipitates at pH 1. Eu " is less acidic and eutopium(II) hydroxide does not precipitate at pH 7—8.5, whereas trivalent lanthanide hydroxides do. Some industrial separations ate based on these phenomena. [Pg.541]

Preparation and Manufacture. Magnesium chloride can be produced in large quantities from (/) camalhte or the end brines of the potash industry (see Potassium compounds) (2) magnesium hydroxide precipitated from seawater (7) by chlorination of magnesium oxide from various sources in the presence of carbon or carbonaceous materials and (4) as a by-product in the manufacture of titanium (see Titaniumand titanium alloys). [Pg.343]

The hydrolysis of the uranyl(VI) ion, UO " 2> has been studied extensively and begins at about pH 3. In solutions containing less than lO " M uranium, the first hydrolysis product is the monomeric U02(OH)", as confirmed using time-resolved laser induced fluorescence spectroscopy. At higher uranium concentrations, it is accepted that polymeric U(VI) species are predominant in solution, and the first hydrolysis product is then the dimer, (U02)2(0H) " 2 (154,170). Further hydrolysis products include the trimeric uranyl hydroxide complexes (U02)3(0H) " 4 and (1102)3(OH)(154). At higher pH, hydrous uranyl hydroxide precipitate is the stable species (171). In studying the sol-gel U02-ceramic fuel process, O nmr was used to observe the formation of a trimeric hydrolysis product, ((U02)3( -l3-0)(p.2-0H)3) which then condenses into polymeric layers of a gel based on the... [Pg.326]

As a result, sulfide precipitation is frequendy used as a polishing step following hydroxide precipitation. [Pg.184]

Assay of beryUium metal and beryUium compounds is usuaUy accompHshed by titration. The sample is dissolved in sulfuric acid. Solution pH is adjusted to 8.5 using sodium hydroxide. The beryUium hydroxide precipitate is redissolved by addition of excess sodium fluoride. Liberated hydroxide is titrated with sulfuric acid. The beryUium content of the sample is calculated from the titration volume. Standards containing known beryUium concentrations must be analyzed along with the samples, as complexation of beryUium by fluoride is not quantitative. Titration rate and hold times ate critical therefore use of an automatic titrator is recommended. Other fluotide-complexing elements such as aluminum, sUicon, zirconium, hafnium, uranium, thorium, and rate earth elements must be absent, or must be corrected for if present in smaU amounts. Copper-beryUium and nickel—beryUium aUoys can be analyzed by titration if the beryUium is first separated from copper, nickel, and cobalt by ammonium hydroxide precipitation (15,16). [Pg.68]

The ferrous ions that dissolve from the anode combine with the hydroxide ions produced at the cathode to give an iron hydroxide precipitate. The active surface of ferrous hydroxide can absorb a number of organic compounds as well as heavy metals from the wastewater passing through the cell. The iron hydroxide and adsorbed substances are then removed by flocculation and filtration. The separation process was enhanced by the addition of a small quantity of an anionic polymer. [Pg.383]

If the amines are required as their hydrochlorides, picrates can often be decomposed by suspending them in acetone and adding two equivalents of ION HCl. The hydrochloride of the base is filtered off, leaving the picric acid in the acetone. Dowex No 1 anion-exchange resin in the chloride form is useful for changing solutions of the more soluble picrates (for example, of adenosine) into solutions of their hydrochlorides, from which sodium hydroxide precipitates the free base. [Pg.57]

OH- ions combine with ions of some metals to form insoluble metal hydroxides (precipitation). Precipitated metals settle out and thus are removed from the water adsorption, using activated carbon, improves this separation process. Iron is one of many metals which is commonly removed in this way. [Pg.84]

Clay - The use of elay based floeculating agent(s) in eonjunetion with a strong metal preeipitator has proven sueeessful in many wastewater treatment applieations where the objeetives are aimed at metals removal. Clay based floeeulants eleans the wastewater and in some eases replaees multistage conventional treatment system and saves the traditional operational difficulties of treatment with several chemicals such as metal hydroxide precipitation, coagulant, floeeulants and other methods. Commercial clay-based floeeulants usually consist of bentonite and other... [Pg.114]

No other oxide phases below MO2 have been established but a yellow hydroxide , precipitated by alkali from aqueous solutions of chromium(II), spontaneously evolves H2 and forms a chromium(III) species of uncertain composition. The sulfides, selenides and tellurides of this triad are considered on p. 1017. [Pg.1009]

Ferrous hydroxide precipitates from solution. Since this compound is unstable in oxygenated solution, it is oxidized to the ferric salt ... [Pg.1301]

The effect of hydrolysis, as a function of pH, on the concentration of hydrated Pu cationic species. The initial (log [Pu] at pH = 0) concentrations are those at pH 8 which correspond to the k values of the hydroxide precipitate of each species. [Pg.221]

In figure 7 a procedure was described for aspirating a sample from a capillary tube and simultaneously adding zinc sulfate and barium hydroxide solutions in order to produce a Somogyi filtrate. Aliquots of the supernatant are suitable for assay for glucose and urea by various procedures. The reason for this is the fact that zinc hydroxide precipitates uric acid, creatinine and other substances, such as low molecular polypeptides, along with the proteins, so that there results a solution which is clear with relatively few components. [Pg.120]

The aqueous decomposition of thiourea to sulfide and cyanamide has been found to be catalyzed by metal hydroxide species and colloidal metal hydroxide precipitates. Kitaev suggested that Cd(OH)2 is actually required for CdS film formation to occur by adsorption of thiourea on the metal hydroxide particles, followed by decomposition of the Cd(OH)2-thiourea complex to CdS. Kaur et al. [241] found... [Pg.133]


See other pages where Hydroxides, precipitation is mentioned: [Pg.242]    [Pg.385]    [Pg.436]    [Pg.350]    [Pg.354]    [Pg.178]    [Pg.179]    [Pg.279]    [Pg.7]    [Pg.164]    [Pg.260]    [Pg.263]    [Pg.368]    [Pg.154]    [Pg.2033]    [Pg.83]    [Pg.391]    [Pg.1049]    [Pg.203]    [Pg.372]    [Pg.41]    [Pg.7]    [Pg.294]    [Pg.865]    [Pg.870]    [Pg.41]    [Pg.485]    [Pg.21]    [Pg.592]    [Pg.601]    [Pg.141]    [Pg.141]    [Pg.395]    [Pg.82]    [Pg.116]   
See also in sourсe #XX -- [ Pg.243 , Pg.245 , Pg.368 ]

See also in sourсe #XX -- [ Pg.655 ]




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Aluminum hydroxide precipitates

Aluminum hydroxide surface precipitates Metal

Aluminum hydroxides precipitation

Complexation—Precipitation Interaction Formation of Insoluble Oxides and Hydroxides

Double metal hydroxides, precipitation

Ferric hydroxide precipitation

Hafnium hydroxide, precipitation

Hydroxide homogeneous precipitant

Hydroxide precipitates

Hydroxide precipitates

Layered double hydroxide precipitate

Metal hydroxide , precipitation

Metal-hydroxide precipitates

Metal-hydroxide precipitates phases

Metal-hydroxide surface precipitates

Metal-hydroxide surface precipitates formation

PH Range for Precipitation of Metal Hydroxides and Oxides

Precipitate, aluminium hydroxide

Precipitate, aluminium hydroxide solubility

Precipitation from solutions niobium hydroxide

Precipitation from solutions tantalum hydroxide

Precipitation of hydroxides by ammonia solution

Precipitation of metal hydroxides and oxides

Precipitation, with barium hydroxide

Sodium hydroxide precipitation

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