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Water adding salt

At p = 1 atm, pure water boils at 100 °C. But salt water boils at a higher temperature. This is a another manifestation of the colligative principle that salt reduces the vapor pressure of water. Adding salt reduces water s tendency to vaporize, so salt water remains a liquid at 100 °C. To model this, start with the condition for the boiling equilibrium of a solution containing a concentration Xb of B at temperature T and at vapor pressure p,... [Pg.285]

Natural gas and its combustion properties appear to have been known since early times (2). Some early temples of worship were located in areas where gas was seeping from the ground or from springs, and it is reported that Julius Caesar saw a phenomenon called the "burning spring" near Grenoble, France. Gas wells were drilled in Japan as early as 615 AD and in 900 AD the Chinese employed bamboo tubes to transport natural gas to their salt works, where the heat was used to evaporate water from salt brine. The existence of natural gas in the United States was reported by early setders who observed gas seeps and columns of fire in the Ohio Valley and the Appalachian area in 1775 (3). [Pg.167]

Although most greases offer some inherent protection against msting, additives, eg, amine salts, sodium sulfonate, cycloparaffin (naphthenate) salts, esters, and nonionic surfactants (qv), are often used to provide added protection against water and salt-spray corrosion. A dispersion of sodium nitrite has been particularly effective in some multipurpose greases. [Pg.247]

Water. Water is often added to processed meat products for a variety of reasons. It is an important carrier of various ionic components that are added to processed meat products. The retention of water during further processing of meat is necessary to obtain a product that is juicy and has higher yields. The amount of water added during the preparation of processed meat products depends on the final properties desired. Water may be added to a meat product as a salt brine or as ice during the comminution step of sausage preparation. [Pg.32]

In the production of sodium 3-hydroxy-2,7-naphthaIenedisulfonate/7Jj5 -j5 -J7 (R-salt) (38), 2-naphthol is stirred with excess 98 wt % sulfuric acid at 60°C, sodium sulfate is added, and the mixture is stirred and heated for 36 h at 105—122°C (77). The charge is diluted with water and salted out with ca 15 wt % sodium chloride at 60°C to give R-salt in 68% yield. [Pg.500]

Osmotic Pressure Controlled Oral Tablets. Alza Corp. has developed a system that is dependent on osmotic pressure developed within a tablet. The core of the tablet is the water-soluble dmg encapsulated in a hydrophobic, semipermeable membrane. Water enters the tablet through the membrane and dissolves the dmg creating a greater osmotic pressure within the tablet. The dmg solution exits at a zero-order rate through a laser drilled hole in the membrane. Should the dmg itself be unable to provide sufficient osmotic pressure to create the necessary pressure gradient, other water-soluble salts or a layer of polymer can be added to the dmg layer. The polymer swells and pushes the dmg solution through the orifice in what is known as a push-pull system (Fig. 3). The exhausted dmg unit then passes out of the body in fecal matter. [Pg.231]

Water-soluble salts are best purified by preparing a concentrated aqueous solution to which, after decolorising with charcoal and filtering, ethanol or acetone is added so that the salts crystallise. They are collected, washed with aqueous ethanol or aqueous acetone, and dried. In some cases, water-soluble salts can be recrystallised satisfactorily from alcohols. Water-insoluble salts are purified by Soxhlet extraction, first with organic solvents and then with water, to remove soluble contaminants. The purified salt is recovered from the thimble. [Pg.68]

R-(-)-Phenylglycinol (5 g, 36.5 mmol) was added to a solution of Zincke salt 115 (10.3 g, 33.3 mmol) in n-butanol (100 mL) at 20 °C. The resulting deep red solution was refluxed during 20 h. Removal of the solvent under reduced pressure left a residue that was treated with HpO (70 mL). The precipitate (2,4-dinitroaniline hydrochloride) was eliminated by filtration, and the operation was repeated twice. The combined aqueous phase was basified with concentrated ammonia (5 mL) and washed twice with EtOAc (200 mL) in order to remove the remaining 2,4-dinitroaniline and the excess of R- )-phenylglycinol. Evaporation of water gave salt 122 (7.53 g, 86%) as a pale orange gum. [Pg.373]

The reaction flask was washed with a solution of 25 grams of sodium hydroxide in 250 cc of water. The combined alkaline solutions were heated to boiling for 5 minutes. A small amount (6 grams) of alkali-insoluble material remained and was filtered off. Sulfuric acid (62% H2SO4 content) was then added at room temperature dropwise under stirring to the filtrate until a pH of 10.3 was reached. This required about BO grams of the acid. The monosodium salt of bis-(3,5,6-trichloro-2-hvdroxyphenyl) methane precipitated out of solution and was filtered and then washed with 200 cc of water. The salt was then sus-... [Pg.760]

To accelerate the polymerization process, some water-soluble salts of heavy metals (Fe, Co, Ni, Pb) are added to the reaction system (0.01-1% with respect to the monomer mass). These additions facilitate the reaction heat removal and allow the reaction to be carried out at lower temperatures. To reduce the coagulate formation and deposits of polymers on the reactor walls, the additions of water-soluble salts (borates, phosphates, and silicates of alkali metals) are introduced into the reaction mixture. The residual monomer content in the emulsion can be decreased by hydrogenizing the double bond in the presence of catalysts (Raney Ni, and salts of Ru, Co, Fe, Pd, Pt, Ir, Ro, and Co on alumina). The same purpose can be achieved by adding amidase to the emulsion. [Pg.68]

Further mechanistic evidence was provided by Benkeser and Krysiak658, who determined the effects of added salts and water on the rates of cleavage of xylyltrimethylsilanes by p-toluenesulphonic acid in acetic acid at 25 °C, the progress of the reaction being followed by dilatometry the first-order rate coefficients are given in Table 227. Clearly the addition of water retards the reaction, as... [Pg.325]

To reverse this half-reaction and bring about the oxidation of water, we need an applied potential difference of at least 0.82 V. Suppose the added salt is sodium chloride. When Cl ions are present at 1 mol-L 1 in water, is it possible that they, and not the water, will be oxidized From Table 12.1, the standard potential for the reduction of chlorine is Cl.36 V ... [Pg.631]

Many substances that participate in aqueous reactions are soluble salts. These ionic solids dissolve in water to give solutions of cations and anions. For almost all salts, there is an upper limit to the amount that will dissolve in water. A salt solution is saturated when the amount dissolved has reached this upper limit of solubility. Any additional salt added to a saturated solution remains undissolved at the bottom of the vessel. When excess solid... [Pg.1186]

Special formulations have been developed for cementing operations in arctic regions or for deep water applications [206,208,256,720,739,1792]. In low-temperature formations, wherein the cement is subjected to freeze-thaw cycling, freezing-point depressants must be added. Salts may serve as such, but traditional organic freezing-point depressants, such as ethylene glycol, also may be added [1022-1024]. [Pg.133]

An inhomogeneous mixture of the dry salt with a little water exploded violently after 30 min [1], This was probably owing to exothermic decarboxylation generating the ad-salt of nitromethane, which is explosively unstable. The decomposition of sodium nitroacetate proceeds exothermically above 80° C [2],... [Pg.257]

Traditionally, butter was made by allowing cream to separate from the milk by standing the milk in shallow pans. The cream is then churned to produce a water in oil emulsion. Typically butter contains 15% of water. Butter is normally made either sweet cream or lactic, also known as cultured, and with or without added salt. Lactic butter is made by adding a culture, usually a mixture of Streptococcus cremoris, S. diacetylactis and Betacoccus cremoris. The culture produces lactic acid as well as various flavouring compounds, e.g. diacetyl, which is commonly present at around 3 ppm. As well as any flavour effect the lactic acid inhibits any undesirable microbiological activity in the aqueous phase of the butter. Sweet cream butter has no such culture added but 1.5 to 3% of salt is normally added. This inhibits microbiological problems by reducing the water activity of the aqueous phase. It is perfectly possible to make salted lactic butter or unsalted sweet cream butter if required. In the UK most butter is sweet cream while in continental Europe most butter is lactic. [Pg.111]

Chevrier et al., 1983), solvent effects (Bensaude et al., 1979), and the effect of added salt on the rate of reaction (Bensaude et al., 1978) have been studied to provide information about this process. Molecular-orbital calculations confirm that a suitable transition state for the reaction is one involving bridging water molecules (Field et al., 1984). [Pg.204]

Congo Red.1—Dissolve 4-6 g. of benzidine in a hot mixture of 12 c.c. of concentrated hydrochloric acid and 100 c.c. of water, add 150 c.c. more water, cool the clear solution to 2°-3°, and diazotise with 3-6 g. of sodium nitrite in 20 c.c. of water, added within the space of one minute. Leave the tetrazo -solution for five minutes and then pour it with stirring into a solution of 16 g. of sodium naph-thionate and 20 g. of crystallised sodium acetate in 250 c.c. of water. When a sample of the liquid, on warming with hydrochloric acid, no longer evolves nitrogen, dissolve the blue-black precipitate of the dye-acid by warming with sodium carbonate and so produce the red sodium salt filter and salt out the product from the filtrate with common salt (not too much). Collect the precipitate at the pump and wash with brine. The blue acid can be precipitated from the solution of the sodium salt with hydrochloric acid. [Pg.302]


See other pages where Water adding salt is mentioned: [Pg.204]    [Pg.47]    [Pg.176]    [Pg.446]    [Pg.7]    [Pg.490]    [Pg.185]    [Pg.474]    [Pg.491]    [Pg.372]    [Pg.331]    [Pg.216]    [Pg.288]    [Pg.592]    [Pg.72]    [Pg.493]    [Pg.190]    [Pg.201]    [Pg.325]    [Pg.182]    [Pg.856]    [Pg.528]    [Pg.60]    [Pg.25]    [Pg.309]    [Pg.198]    [Pg.52]    [Pg.174]    [Pg.220]    [Pg.323]    [Pg.218]    [Pg.96]    [Pg.94]   
See also in sourсe #XX -- [ Pg.466 ]




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