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Solutions insoluble

In the United States, Hquid HLW from the reprocessing of defense program fuels was concentrated, neutralized with NaOH, and stored in underground, mild steel tanks pending soHdification and geologic disposal (see Tanks AND PRESSURE VESSELS). These wastes are a complex and chemically active slurry. Suspended in the supernatant Hquid are dissolver soHds which never went into solution, insoluble reaction products which formed in the tank, and salts which have exceeded their solubiHty limit. The kinetics of many of the reactions taking place are slow (years) so that the results of characterization... [Pg.206]

The anodic behaviour of Pb varies depending upon the electrolyte composition and the electrode potential and has been the subject of a number of reviews . In NO,", CHjCOO and BF4" solutions, lead will form highly soluble lead salts whilst in Cl" and 804 solutions, insoluble lead salts are formed when Pb is anodically polarised. [Pg.180]

In determinations of sulphurous acid and sulphites, excess of standard 0.05M iodine is diluted with several volumes of water, acidified with hydrochloric or sulphuric acid, and a known volume of the sulphite or sulphurous acid solution is added slowly and with constant stirring from a burette, with the jet close to the surface of the liquid. The excess of iodine is then titrated with standard 0.1M sodium thiosulphate. Solid soluble sulphites are finely powdered and added directly to the iodine solution. Insoluble sulphites (e.g. calcium sulphite) react very slowly, and must be in a very fine state of division. [Pg.398]

A, B, S refer to solute, insoluble solid, solvent respectively 1refer to liquid overflow or underflow from units 1, 0 refers to the liquid underflow feed to unit 1. [Pg.541]

Erlenmeyer synthesis org chem Preparation of cyclic ethers by the condensation of an aldehyde with an a-acylamino acid in the presence of acetic anhydride and sodium acetate. 3r-l3n,mT-3r sin-th3-s3s erucic acid org chem C22H42O2 A monoethenoid acid that is the cis isomer of bras-sidic acid and makes up 40 to 50% of the total fatty acid in rapeseed, wallflower seed, and mustard seed crystallizes as needles from alcohol solution, insoluble in water, soluble in ethanol and methanol. o rus ik as ad erythrite See erythritol. er o.thrTt ... [Pg.139]

Organic matter extracted from earth materials usually is fractionated on the basis of solubility characteristics. The fractions commonly obtained include humic acid (soluble in alkaline solution, insoluble in acidic solution), fulvic acid (soluble in aqueous media at any pH), hymatomelamic acid (alcohol-soluble part of humic acid), and humin (insoluble in alkaline solutions). This operational fractionation is based in part on the classical definition by Aiken et al. (1985). It should be noticed, however, that this fractionation of soil organic matter does not lead to a pure compound each named fraction consists of a very complicated, heterogeneous mixture of organic substances. Hayes and Malcom (2001) emphasize that biomolecules, which are not part of humic substances, also may precipitate at a pH of 1 or 2 with the humic acids. Furthermore, the more polar compounds may precipitate with fulvic acids. [Pg.15]

White gelatinous precipitate decomposes on heating, forming oxide soluble in acids and ammonium carbonate solution insoluble in alkalis. [Pg.202]

White lustrous needles or fibrous mass hygroscopic density 2.88 g/cm melts at 814°C vaporizes at 1,300°C highly soluble in water, forming blue solution insoluble in ether. The tetrahydrate occurs in blue hygroscopic crystalline form, that changes to green modification above 38°C decomposes to trdiydrate at 51°C soluble in water. [Pg.219]

Pale green hexagonal crystals (in partially oxidized form) or white amorphous powder (when pure) density 3.4g/cm3 decomposes on heating insoluble in water (1.5 mg/L at 20°C), Ksp 8.0 x IQ i soluble in acids moderately soluble in ammonium salt solutions insoluble in alkalies. [Pg.429]

C vaporizes at 3,600°C electrical resistivity l.SxlQi ohm-cm at 27°C practically insoluble in water (86 mg/L at 30° C) soluble in acids and ammonium salt solutions insoluble in alcohol. [Pg.530]

Colorless crystals or white powder monoclinic structure density 3.90 g/cm3 stable at ordinary temperatures melts at 560°C with partial decomposition, releasing oxygen moderately soluble in cold water 4.74 g/lOOmL at 0°C greater solubility in boiling water 32.3 g/lOOmL at 100°C soluble in potassium iodide solution insoluble in alcohol and liquid ammonia... [Pg.760]

The octahydrate consists of colorless, tetragonal, deliquescent crystals density 1.90 g/cm loses all its water molecules at 100°C sparingly soluble in water at low temperatures, 0.90 g/100 mL at 0°C soluble in boiling water, 47.7 g/100 mL at 100°C aqueous solution highly alkahne soluble in acids and in ammonium chloride solution insoluble in acetone. [Pg.887]

C insoluble in water (about 5mg/L at 20°C) soluble in alkalies, potassium cyanide and ammonia solutions insoluble in alcohol. [Pg.987]

This aminopropanol treatment for removal of bound gossypol appeared to be an excellent means to test the role of bound gossypol in the color problem. The water and salt-solution insoluble fraction (l) of LCP flour that contained the brown color causing pigments was treated for 15 min at 80°C with 2Z... [Pg.35]

Figure 13. Biscuits containing the water and salt-solution insoluble fraction of LCP cottonseed flour before and after treatment with aminopropanol (4.5%)... Figure 13. Biscuits containing the water and salt-solution insoluble fraction of LCP cottonseed flour before and after treatment with aminopropanol (4.5%)...
Strontium sulfate, [CAS 7759-02-6], Sr SO/. white precipitate (K p — 3.2 x 10-7), formed by reaction of strontium salt solution and H2S04 or sodium sulfate solution, insoluble in acids. On heating with carbon strontinm sulfate yields strontium sulfide, SrS, while on boiling with sodium carbonate solution, SrS04 yields strontinm carbonate. [Pg.1554]

MW 129.02 CAS [108-80-5] solid crystals which may occur as dihydrate loses water of crystallization on exposure to air, evolves cyanic acid on heating does not melt slightly soluble in cold water (0.5%) but much more soluble in hot water soluble in pyridine, hot alcohols, HC1, H2S04, and caustic soda solution insoluble in cold methanol, ether, benzene, acetone, and chloroform. [Pg.308]

Manganese dioxide + sulfuric acid Silver nitrate Reddish-brown bromine vapors evolve upon mild heating Pale yellow, curdy, precipitate of silver bromide slightly soluble in ammonia solution insoluble in nitric acid... [Pg.529]

Silver nitrate Brownish red precipitate of silver chromate soluble in dilute nitric acid and in ammonia solution insoluble in acetic acid... [Pg.530]

Calcium chloride solution white, crystalline precipitate of calcium oxalate from neutral solutions, insoluble in dilute acetic acid, oxalic acid, and in ammonium oxalate solution, but soluble in dilute hydrochloric acid and in dilute nitric acid. It is the most insoluble of all oxalates (0 0067 g t 1 at 13°) and is even precipitated by calcium sulphate solution and acetic acid. Barium chloride solution similarly gives a white precipitate of barium oxalate sparingly soluble in water (0 016 g t-1 at 8°), but soluble in solutions of acetic and of oxalic acids. [Pg.370]

Antifoams can be divided into two groups. The first group includes substances, for which the principle of defoaming action is based on the interaction with the foaming agent resulting in formation of insoluble or poorly soluble compounds. For instance, if soluble calcium or aluminium salts (chlorides) are added to the foaming solution of sodium or potassium salts of fatty acids, or cationic surfactants to anionic surfactants solution, insoluble compounds are formed and the foam is destroyed [6]. The less soluble compound formed, the more efficient the antifoam is. [Pg.611]

Modified from Ref. T35. "Other components mainly P2O5 (0.2%) other phases mainly alkalis (adsorbed or in solution), insoluble residue and PjO (form of combination unknown). Fe HP = hydrogarnet-type product from ferrite phase. Mg HP = hydrotalcite-type phase. AFm and Mg HP include poorly crystalline materials intimately mixed with C-S-H. Discrepancies in totals arise from rounding. [Pg.219]

Solubihty practically insoluble in ethanol (95%) and in ether. Dissolves in a solution of sodium hydroxide (1 in 10) and produces a viscous solution. Insoluble, but swells in water. [Pg.342]

Properties Filamentous, grainy, granular or powder, colorless or slightly yellow, may have a slight characteristic smell and taste. Slowly soluble in water forming a viscous solution. Insoluble in alcohol. [Pg.66]

Properties White powder. Mp 170C (decomposes). Soluble in hydrochloric acid and alkali tartrate solutions insoluble in alcohol, ether, and water. [Pg.92]

Properties Grayish-black, metallic, glistening crystals. D 5.778 (15C) sublimes at 438C. Soluble in alcohol, hydriodic acid, and potassium iodide solutions insoluble in water. Decomposes in hot water. [Pg.162]

Properties Red-brown powder or large black shiny crystals green luster. Mp 117C. Soluble in alcohol and water, giving orange-brown solutions insoluble in ether. [Pg.302]

Properties White to brownish-yellow powder. D 5.653 (15C), bp 1290C,mp 606C. Soluble in ammonia and potassium iodide solutions insoluble in water. [Pg.352]

Properties Pure product is crystalline light-brown color. Mp 131C, d 1.24. Commercial grade is 50% aqueous solution. Insoluble in organic solvents. [Pg.609]

Properties White powder sweet taste. Forms a dextrorotatory colloidal solution insoluble in alcohol soluble in water. [Pg.615]


See other pages where Solutions insoluble is mentioned: [Pg.147]    [Pg.84]    [Pg.27]    [Pg.277]    [Pg.341]    [Pg.185]    [Pg.265]    [Pg.26]    [Pg.35]    [Pg.172]    [Pg.748]    [Pg.147]    [Pg.425]    [Pg.228]    [Pg.210]    [Pg.359]    [Pg.683]    [Pg.585]   
See also in sourсe #XX -- [ Pg.188 ]




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Sulfides insoluble in basic solution

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