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Hydrous

The JP 2001 describes hydrous lanolin as a mixture of lanolin and 25-30% w/w purified water. The PhEur 2005 describes hydrous lanolin as a mixture of lanolin and 25% w/w purified water see also Section 18. The PhEur 2005 additionally permits the inclusion of up to 150 ppm of butylated hydroxy-toluene as an antioxidant. [Pg.404]

Hydrous lanolin is widely used in topical pharmaceutical formulations and cosmetics in applications similar to those for lanolin. [Pg.404]

Hydrous lanolin is commonly used in the preparation of water-in-oil creams and ointments. More water may be incorporated into hydrous lanolin than into lanolin. [Pg.404]

Hydrous lanolin is a pale yellow-colored, unctuous substance with a faint characteristic odor. When melted by heating on a water bath, hydrous lanolin separates into a clear oily layer and a clear water layer. [Pg.404]

Solubility practically insoluble in chloroform, ether, and water. Only the fat component of hydrous lanolin is soluble in organic solvents. [Pg.404]


Matijevi i E 1976 Preparation and oharaoterization of monodispersed metal hydrous oxide sols Prog. Colloid Polym. Sol. 61 24-35... [Pg.2690]

Scandium is not an uncommon element, but is difficult to extract. The only oxidation state in its compounds is -I- 3, where it has formally lost the 3d 4s electrons, and it shows virtually no transition characteristics. In fact, its chemistry is very similar to that of aluminium (for example hydrous oxide SC2O3, amphoteric forms a complex [ScFg] chloride SCCI3 hydrolysed by water). [Pg.369]

Alkali metal ferrates(VI), for example K2pe04, are obtained by oxidation of a suspension of hydrous iron(III) oxide (assumed to be Fe(OH)3 in the equation below) by chlorate(I) in concentrated alkali ... [Pg.393]

Metal organic decomposition (MOD) is a synthesis technique in which metal-containing organic chemicals react with water in a nonaqueous solvent to produce a metal hydroxide or hydrous oxide, or in special cases, an anhydrous metal oxide (7). MOD techniques can also be used to prepare nonoxide powders (8,9). Powders may require calcination to obtain the desired phase. A major advantage of the MOD method is the control over purity and stoichiometry that can be achieved. Two limitations are atmosphere control (if required) and expense of the chemicals. However, the cost of metal organic chemicals is decreasing with greater use of MOD techniques. [Pg.310]

Hexafluoroantimonic acid [72121 -43-8] HSbF 6H20, is prepared by dissolving freshly prepared hydrous antimony pentoxide ia hydrofluoric acid or adding the stoichiometric amount of 70% HF to SbF. Both of these reactions are exothermic and must be carried out carefully. [Pg.151]

FIuorosihca.tes, Compared to the simple sUicates, these crystals have more complex chain and sheet stmctures. Examples from nature iaclude hydrous micas and amphiboles, including hornblende and nephrite jade. In glass-ceramics, fluorine replaces the hydroxyl ion fluorine is much easier to iacorporate ia glass and also makes the crystals more refractory. Eour commercial fluorosUicate glass-ceramic compositions and thek properties are Usted ia Table 2. [Pg.322]

Fluorozirconate Crystallization. Repeated dissolution and fractional crystallization of potassium hexafluorozirconate was the method first used to separate hafnium and zirconium (15), potassium fluorohafnate solubility being higher. This process is used in the Prinieprovsky Chemical Plant in Dnieprodzerzhinsk, Ukraine, to produce hafnium-free zirconium. Hafnium-enriched (about 6%) zirconium hydrous oxide is precipitated from the first-stage mother Hquors, and redissolved in acid to feed ion-exchange columns to obtain pure hafnium (10). [Pg.442]

Hafnium dioxide is formed by ignition of hafnium metal, carbide, tetrachloride, sulfide, boride, nitride, or hydrous oxide. Commercial hafnium oxide, the product of the separation process for zirconium and hafnium, contains 97—99% hafnium oxide. Purer forms, up to 99.99%, are available. [Pg.445]

The hydrous oxide, Hf02 xH20, is precipitated from acidic solutions by addition of ammonium hydroxide or dilute alkaline solutions. However, the hydrous oxide exhibits a limited solubihty in strongly alkaline solutions (65). The existence and relative stabiUty of soluble alkaline peroxy compounds has been demonstrated (66). [Pg.445]

The best known oxoanion of iron is the ferrate(VI) prepared by oxidizing a suspension of hydrous iron(III) oxide in concentrated alkah with potassium hypochlorite or by anodic oxidation of iron in concentrated alkah. Crystals of potassium ferrate [13718-66-6], K FeO, are deep purple, orthorhombic, and contain discrete tetrahedral [FeOJ anions. Barium ferrate [13773-23A] can be precipitated from solutions of soluble ferrate salts. [Pg.437]

The quantities of magnesium sulfate (anhydrous and hydrous) shipped and used in the United States during the period 1989—1993 were (52,103,130) ... [Pg.357]

The Mn ion is so unstable that it scarcely exists in aqueous solution. In acidic aqueous solution, manganic compounds readily disproportionate to form Mn ions and hydrated manganese(IV) oxide, Mn02 2H20 in basic solution these compounds hydroly2e to hydrous manganese(III) oxide, MnO(OH). Sulfuric acid concentrations of about 400 450 g/L are required to stabilize the noncomplexed Mn ion in aqueous solutions. [Pg.506]

Fig. 2. Hydration of the surface stmcture of manganese dioxide (2) and subsequent reactions of hydrous manganese oxide (3) showing proton transfer (4)... Fig. 2. Hydration of the surface stmcture of manganese dioxide (2) and subsequent reactions of hydrous manganese oxide (3) showing proton transfer (4)...
Ion Ionic radius, pm CoUoidal hydrous manganese dioxide, mol/mol Hydrated radius, pm 5-Mn02, )J.mol/g... [Pg.510]

Figure 17 summarizes the avadable sol—gel processes (56). The process on the right of the figure involves the hydrolysis of metal alkoxides in a water—alcohol solution. The hydrolyzed alkoxides are polymerized to form a chemical gel, which is dried and heat treated to form a rigid oxide network held together by chemical bonds. This process is difficult to carry out, because the hydrolysis and polymerization must be carefully controlled. If the hydrolysis reaction proceeds too far, precipitation of hydrous metal oxides from the solution starts to occur, causing agglomerations of particulates in the sol. [Pg.69]

A gel is defined as a hydrous metal aluminosihcate prepared from either aqueous solutions, reactive soflds, colloidal sols, or reactive aluminosihcates such as the residue stmcture of metakaolin and glasses. [Pg.451]

Uranium Purification. Subsequent uranium cycles provide additional separation from residual plutonium and fission products, particularly zirconium— niobium and mthenium (30). This is accompHshed by repeating the extraction/stripping cycle. Decontamination factors greater than 10 at losses of less than 0.1 wt % are routinely attainable. However, mthenium can exist in several valence states simultaneously and can form several nitrosyl—nitrate complexes, some for which are extracted readily by TBP. Under certain conditions, the nitrates of zirconium and niobium form soluble compounds or hydrous coUoids that compHcate the Hquid—Hquid extraction. SiUca-gel adsorption or one of the similar Hquid—soHd techniques may also be used to further purify the product streams. [Pg.206]

A. K. Burnham, Relationship Between Hydrous and Ordinay Pyrolysis, UCRL-JC-114130, Lawrence Livermore National Laboratory, Livermore, Calif.,... [Pg.357]

The petroleum generation process can be dupHcated by laboratory pyrolysis. Higher temperatures are needed to produce these reactions in a few hours or days rather than the millions of years in nature (16,17). Both dry pyrolysis and hydrous pyrolysis have been used. [Pg.161]

In the double-neutralization process, Na2SiFg is precipitated and removed by filtration at a pH of 3—4 (9). Upon raising the pH to 7—9, insoluble phosphates of Fe, Al, Ca, and Mg form and separate. Iron can be precipitated as hydrous ferric oxide, reducing the phosphate loss at the second filter cake. Both the fluorosihcate and metal phosphate filter residues tend to be voluminous cakes that shrink when dewatered recovery of soluble phosphates trapped within the cakes is difficult. [Pg.328]


See other pages where Hydrous is mentioned: [Pg.265]    [Pg.353]    [Pg.2669]    [Pg.1146]    [Pg.1170]    [Pg.495]    [Pg.495]    [Pg.495]    [Pg.1090]    [Pg.566]    [Pg.441]    [Pg.445]    [Pg.412]    [Pg.497]    [Pg.500]    [Pg.413]    [Pg.437]    [Pg.344]    [Pg.344]    [Pg.487]    [Pg.508]    [Pg.510]    [Pg.510]    [Pg.510]    [Pg.510]    [Pg.520]    [Pg.521]    [Pg.525]    [Pg.131]    [Pg.284]    [Pg.93]   
See also in sourсe #XX -- [ Pg.7 , Pg.227 ]

See also in sourсe #XX -- [ Pg.306 ]




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Adsorption hydrous manganese oxide

Alumina hydrous

Aluminium hydrous oxides

Aluminum silicate hydrous

Basalt melting, hydrous

Bismuth, hydrous oxides

Chelates/complexes of hydrous

Chromic oxide hydrous

Chromium oxide, hydrous

Chromium oxide, hydrous catalytic activity

Coated particles hydrous oxide

Colloidal hydrous ferric and manganese oxides

Colloidal hydrous manganese oxide

Coordination chemistry hydrous oxide

Dehydration of hydrous oxides

Films, hydrous

Formation of Hydrous Oxides

Glasse hydrous

H NMR of Hydrous Glasses

Hydrogenation activities, hydrous titanium

Hydrous Chromia on Hematite

Hydrous Niobia

Hydrous Tin Oxide

Hydrous aluminum oxide

Hydrous benefits

Hydrous calcium silicate

Hydrous ethanol

Hydrous features

Hydrous ferric oxide

Hydrous ferric oxide hydroxide

Hydrous ferrous oxide

Hydrous gels

Hydrous glasses

Hydrous gold oxide

Hydrous iron oxides

Hydrous kaolin

Hydrous lanolin

Hydrous magnesium calcium silicate

Hydrous magnesium silicate

Hydrous metal oxides

Hydrous metal oxides supports

Hydrous mica

Hydrous minerals

Hydrous nickel oxides 1-hydroxide

Hydrous nickel oxides materials

Hydrous oxide control model

Hydrous oxide films

Hydrous oxide gels

Hydrous oxide growth

Hydrous oxide growth mechanisms

Hydrous oxide growth on platinum

Hydrous oxide solid-phase adsorbents

Hydrous oxide solid-phase adsorbents adsorbate

Hydrous oxide surface

Hydrous oxides

Hydrous oxides acid strength

Hydrous oxides adsorption

Hydrous oxides adsorption characteristics

Hydrous oxides colloidal

Hydrous oxides colloidal precipitates

Hydrous oxides heavy metals

Hydrous oxides isotherms

Hydrous oxides nuclide adsorption

Hydrous oxides of aluminum

Hydrous oxides of iron and manganese

Hydrous oxides silicon

Hydrous oxides solubility effects

Hydrous oxides structural aspects

Hydrous silicate

Hydrous sodium lithium magnesium

Hydrous sodium lithium magnesium silicate

Hydrous sodium polysilicates

Hydrous sodium polysilicates granules

Hydrous sodium polysilicates powders

Hydrous sodium titanate ion-exchange

Hydrous species reaction

Hydrous species reaction in rhyolitic melt

Hydrous titanium oxide

Hydrous titanium oxide catalysts

Hydrous titanium oxide supported

Hydrous titanium oxide supported catalysts

Hydrous wool

Hydrous wool fat

Incipient hydrous oxide/adatom mediator

Indium hydrous oxide

Ion adsorption by hydrous metal oxides

Iron oxide supports hydrous

Iron phases, amorphous hydrous

Manganese dioxide, hydrous

Manganese hydrous oxides

Mantle hydrous

Metal binding by a hydrous oxide

Metal hydrous oxide particles

Metal ions association with hydrous oxide surfaces

Minerals hydrous mineral

Neptunium hydrous oxide

Nickel hydrous oxide

Niobium oxide, hydrous

Outer Hydrous Layer on the Passive Oxide Film

Outer hydrous layer

Pyrolysis hydrous

Rare earth oxalates hydrous

Reaction Kinetics in Hydrous Environments

Silica hydrous

Species hydrous oxide

Surface hydrous

Tetravalent metals, hydrous oxides

The hydrous oxides of iron and manganese

Titanium hydrous

Titanium oxide supports hydrous

Transport processes in hydrous oxide

Transport processes in hydrous oxide films

Trivalent metals, hydrous oxides

Zirconium hydrous polymers

Zirconium oxide hydrate hydrous

Zirconium oxide supports hydrous

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