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Sodium physical properties

The production of both an alcohol and the sodium salt of an acid might easily be confused with the hydrolysis products of an ester (in the above instance benzyl benzoate). Such an error would soon be discovered (e.g., by reference to the b.p. and other physical properties), but it would lead to an unnecessary expenditure of time and energy. The above example, however, emphasises the importance of conducting the class reactions of neutral oxygen-containing compounds in the proper order, viz., (1) aldehydes and ketones, (2) esters and anhydrides, (3) alcohols, and (4) ethers. [Pg.1063]

The physical properties of cyanoacetic acid [372-09-8] and two of its ester derivatives are Hsted ia Table 11 (82). The parent acid is a strong organic acid with a dissociation constant at 25°C of 3.36 x 10. It is prepared by the reaction of chloroacetic acid with sodium cyanide. It is hygroscopic and highly soluble ia alcohols and diethyl ether but iasoluble ia both aromatic and aUphatic hydrocarbons. It undergoes typical nitrile and acid reactions but the presence of the nitrile and the carboxyUc acid on the same carbon cause the hydrogens on C-2 to be readily replaced. The resulting malonic acid derivative decarboxylates to a substituted acrylonitrile ... [Pg.225]

Standard polyester fibers contain no reactive dye sites. PET fibers are typically dyed by diffusiag dispersed dyestuffs iato the amorphous regions ia the fibers. Copolyesters from a variety of copolymeri2able glycol or diacid comonomers open the fiber stmcture to achieve deep dyeabiHty (7,28—30). This approach is useful when the attendant effects on the copolyester thermal or physical properties are not of concern (31,32). The addition of anionic sites to polyester usiag sodium dimethyl 5-sulfoisophthalate [3965-55-7] has been practiced to make fibers receptive to cationic dyes (33). Yams and fabrics made from mixtures of disperse and cationicaHy dyeable PET show a visual range from subde heather tones to striking contrasts (see Dyes, application and evaluation). [Pg.325]

Cryolite. Cryohte constitutes an important raw material for aluminum manufacturing. The natural mineral is accurately depicted as 3NaF AIF., but synthetic cryohte is often deficient in sodium fluoride. Physical properties are given in Table 4. [Pg.142]

In addition to time-related effects, the soUd-state physical properties are also affected by adsorbed water, which functions as a plasticizer. Water pickup is affected by the nature of the cation, with sodium ionomers absorbing about 10 times the level of the zinc equivalent (6) under the same conditions. Drying must be carried out at temperatures below 100°C and is therefore a slow process. In commercial practice, ionomers are suppUed dry, and techniques have been developed to minimize moisture absorption during processing. [Pg.406]

Other. A large variety of additives are used in paper-coatiag colors primarily to modify the physical properties of the colors (102). At high soHds concentrations in water, mineral pigment particles tend to associate and form viscous pastes. Dispersants (qv) are used to prevent this and to provide low viscosity slurries. Common dispersants include polyphosphates and sodium polyacrylate [9003-04-7]. Various water-soluble polymers are added to coatiag colors and act as water-retention agents and as rheology modifiers. [Pg.22]

Sihcate solutions of equivalent composition may exhibit different physical properties and chemical reactivities because of differences in the distributions of polymer sihcate species. This effect is keenly observed in commercial alkah sihcate solutions with compositions that he in the metastable region near the solubihty limit of amorphous sihca. Experimental studies have shown that the precipitation boundaries of sodium sihcate solutions expand as a function of time, depending on the concentration of metal salts (29,58). Apparently, the high viscosity of concentrated alkah sihcate solutions contributes to the slow approach to equihbrium. [Pg.6]

Only body-centered cubic crystals, lattice constant 428.2 pm at 20°C, are reported for sodium (4). The atomic radius is 185 pm, the ionic radius 97 pm, and electronic configuration is lE2E2 3T (5). Physical properties of sodium are given ia Table 2. Greater detail and other properties are also available... [Pg.161]

Sodium iodide crystallizes ia the cubic system. Physical properties are given ia Table 1 (1). Sodium iodide is soluble ia methanol, ethanol, acetone, glycerol, and several other organic solvents. SolubiUty ia water is given ia Table 2. [Pg.190]

Physical Properties. Anhydrous sodium sulfite [7757-83-7] Na2S02, is an odorless, crystalline soHd and most commercial grades other than by-product materials are colorless or off-white (331—334). It melts only with decomposition. The specific gravity of the pure soHd is 2.633 (15.4°C). Sodium sulfite is quite soluble in water. It has a maximum solubiHty of 28 g/100 g sol at 33.4°C at higher and lower temperatures, it is less soluble in water. Below this temperature, the heptahydrate crystallizes above this temperature, the anhydrous salt crystallizes. Sodium sulfite is soluble in glycerol but insoluble in alcohol, acetone, and most other organic solvents. [Pg.148]

Physical Properties. Sodium metabisulfite (sodium pyrosulfite, sodium bisulfite (a misnomer)), Na2S20, is a white granular or powdered salt (specific gravity 1.48) and is storable when kept dry and protected from air. In the presence of traces of water it develops an odor of sulfur dioxide and in moist air it decomposes with loss of part of its SO2 content and by oxidation to sodium sulfate. Dry sodium metabisulfite is more stable to oxidation than dry sodium sulfite. At low temperatures, sodium metabisulfite forms hydrates with 6 and 7 moles of water. The solubiHty of sodium metabisulfite in water is 39.5 wt % at 20°C, 41.6 wt % at 40°C, and 44.6 wt % at 60°C (340). Sodium metabisulfite is fairly soluble in glycerol and slightly soluble in alcohol. [Pg.149]

Physical Properties. Sodium dithionite (sodium hydrosulfite, sodium sulfoxylate), Na2S204, is a colorless soHd and is soluble in water to the extent of 22 g/100 g of water at 20°C. [Pg.150]

Fig. 4. Physical property curves for aqueous sodium lauryl sulfate where A is detergency B, density change C, conductivity (high frequency) D, surface... Fig. 4. Physical property curves for aqueous sodium lauryl sulfate where A is detergency B, density change C, conductivity (high frequency) D, surface...
Molten sodium is injected into the retort at a prescribed rate and the temperature of the system is controlled by adjusting the furnace power or with external cooling. The variables that control the quaUty and physical properties of the powder are the reduction temperature and its uniformity, diluent type and concentration, sodium feed rate, and stirring efficiency. Optimizing a variable for one powder attribute can adversely affect another property. For example, a high reduction temperature tends to favor improved chemical quaUty but lowers the surface area of the powder. [Pg.327]

Selected physical properties of sodium thiosulfate pentahydrate are shown in Table 1. The crystals are relatively stable, efflorescing in warm, dry air and dehquescing slightly in moist air. They melt in their water of hydration at 48°C and can be completely dehydrated in a vacuum oven at this temperature, or at atmospheric pressure at 105°C. Anhydrous sodium thiosulfate can also be crystallised direcdy from a 72% solution above 75°C. It decomposes at 233°C ... [Pg.28]

Further heating to 440—500°C gives sodium sulfide and sulfur dioxide (33). Table 1. Physical Properties of Sodium Thiosulfate Pentahydrate... [Pg.28]

Despite the fact that many boron hydride compounds possess unique chemical and physical properties, very few of these compounds have yet undergone significant commercial exploitation. This is largely owing to the extremely high cost of most boron hydride materials, which has discouraged development of all but the most exotic appHcations. Nevertheless, considerable commercial potential is foreseen for boron hydride materials if and when economical and rehable sources become available. Only the simplest of boron hydride compounds, most notably sodium tetrahydroborate, NajBHJ, diborane(6), B2H, and some of the borane adducts, eg, amine boranes, are now produced in significant commercial quantities. [Pg.253]

Physical Properties. The physical properties of sodium chlorate [7775-09-9] and potassium chlorate [3811-04-9], KCIO, are summarised ia Table 1 (21). The solubiHties of these chlorates ia water are given ia Figure 2 (22—26). [Pg.495]

Table 1. Physical Properties of Sodium and Potassium Chlorates... Table 1. Physical Properties of Sodium and Potassium Chlorates...
Physical Properties. The physical properties of sodium cyanide are Hsted in Table 4. The soHd phase in contact with a saturated aqueous solution at temperatures above 34.7°C is the anhydrous salt below 34.7°C,the soHd phase is sodium cyanide dihydrate [25178-25-0] NaCH-2H2 0. The solubihty of the dihydrate in grams of sodium cyanide per 100 grams of saturated solution is 26.01, at —15°C 32.8, at 10°C 34.2, at 15°C and 45, at 34.7°C. The solubihty of the anhydrous salt is less dependent on temperature. [Pg.381]

Physical Properties. The physical properties of potassium cyanide are given in Table 6. Unlike sodium cyanide, potassium cyanide does not form a diliydrate. [Pg.384]

Accelerators may be added to improve the physical properties of the polymer when needed. Where high modulus or low oil swell is required, thiocarbanihde is the preferred accelerator, with a cure time of 60 min at 100°C. Tetraethyl thiuram disulfide and sodium dibutyl dithiocarbamate are preferred for high tensile strength and cured at 121°C. [Pg.548]

Vanadium-Sodium Compounds Most Corrosive. Physical property data for vanadates, phase diagrams, laboratory experiments, and numerous field investigations have shown that the sodium vanadates are the lowest melting compounds and are the most corrosive to metals and refractories. These compounds are thought to form by either the vapor phase reaction of NaCI and V2O5 or by the combination of fine droplets of these materials upon the cooler parts of combustion equipment. [Pg.265]


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