Water sodium nitrate

Potassium nitrate. Sulfuric acid. Water Sodium nitrate. Sulfuric acid. Water Nitric acid. Sulfuric acid. Cornstarch, Ammonia Starch, Sulfuric acid. Nitric acid Nitric acid. Sulfuric acid. Cellophane, Cotton, Sodium bicarbonate... 

Figure 3. Difference between experimental and calculated vapor compositions vs. liquid composition for 1-propanol-water-sodium nitrate system...

Poly(A -isopropylacrylamide-co-benzo-15-crown-5-acry lamide) cesium nitrate and water lithium nitrate and water potassium nitrate and water sodium nitrate and water 2008MIP 2008MIP 2008MIP 2008MIP... 

In Table 9.3 the intersection of the lead(II)-ion line and the bromide-ion column shows that lead(II) bromide is insoluble lead(II) bromide forms a solid precipitate, PbBr2(s). The intersection of the sodium-ion line and the nitrate-ion column shows that sodium nitrate is soluble in water sodium nitrate remains in aqueous solution, NaNOjCaq). Both conclusions can also be reached from the solubility guidelines Lead(II) bromide is one of the three insoluble bromides, and all sodium and nitrate compounds are soluble. 

Adams catalyst, platinum oxide, Pt02 H20. Produced by fusion of H2PtCl6 with sodium nitrate at 500-550 C and leaching of the cooled melt with water. Stable in air, activated by hydrogen. Used as a hydrogenation catalyst for converting alkenes to alkanes at low pressure and temperature. Often used on Si02... 

Method 1. From ammonium chloroplatinate. Place 3 0 g. of ammonium chloroplatinate and 30 g. of A.R. sodium nitrate (1) in Pyrex beaker or porcelain casserole and heat gently at first until the rapid evolution of gas slackens, and then more strongly until a temperature of about 300° is reached. This operation occupies about 15 minutes, and there is no spattering. Maintain the fluid mass at 500-530° for 30 minutes, and allow the mixture to cool. Treat the sohd mass with 50 ml. of water. The brown precipitate of platinum oxide (PtOj.HjO) settles to the bottom. Wash it once or twice by decantation, filter througha hardened filter paper on a Gooch crucible, and wash on the filter until practically free from nitrates. Stop the washing process immediately the precipitate tends to become colloidal (2) traces of sodium nitrate do not affect the efficiency of the catalyst. Dry the oxide in a desiccator, and weigh out portions of the dried material as required. 

Method 2. From chloroplatinic acid. Dissolve 3 - 5 g. of the purest commercial chloroplatinic acid (3) in 10 ml. of water contained in a 250 ml. P3rrex beaker or porcelain casserole, and add 35 g. of A.R. sodium nitrate (1), Evaporate the mixture to dryness by heating gently over a Bunsen flame whilst stirring with a glass rod. Then raise the temperature... 

Cautiously add 250 g. (136 ml.) of concentrated sulphuric acid in a thin stream and with stirring to 400 ml. of water contained in a 1 litre bolt-head or three-necked flask, and then dissolve 150 g. of sodium nitrate in the diluted acid. Cool in a bath of ice or iced water. Melt 94 g. of phenol with 20 ml. of water, and add this from a separatory funnel to the stirred mixture in the flask at such a rate that the temperature does not rise above 20°. Continue the stirring for a further 2 hours after all the phenol has been added. Pour oflF the mother liquid from the resinous mixture of nitro compounds. Melt the residue with 500 ml. of water, shake and allow the contents of the flask to settle. Pour oflF the wash liquor and repeat the washing at least two or three times to ensure the complete removal of any residual acid. Steam distil the mixture (Fig. II, 40, 1 or Fig. II, 41, 1) until no more o-nitrophenol passes over if the latter tends to solidify in the condenser, turn oflF the cooling water temporarily. Collect the distillate in cold water, filter at the pump, and drain thoroughly. Dry upon filter paper in the air. The yield of o-nitrophenol, m.p. 46° (1), is 50 g. 

Sodium hypobromite dissolve 100 g of NaOH in 250 mL of water and add 25 mL of bromine. Sodium nitrate, NaN03—Q.5N 43 g per liter. 

Sodium Antimonate. Sodium antimonate [15593-75-6] Na SbO, another antimony synergist of commercial importance, has an antimony content of 61—63 wt % and a bulk density of 39.4—46.4 kg/m. Properties are given in Table 2. It is made by oxidizing antimony trioxide using sodium nitrate and caustic. It is a white powder and has a pH of around 9—11 when dissolved in water. 

Hitec Heat-Transfer Salt. Hitec heat-transfer salt, manufactured by Coastal Chemical Co., is an eutectic mixture of water-soluble inorganic salts potassium nitrate (53%), sodium nitrite (40%), and sodium nitrate (7%). It is suitable for Hquid-phase heat transfer at temperatures of 150—540°C. 

Selected physical and chemical properties of sodium nitrate are Hsted in Table 1. At room temperature, sodium nitrate is an ododess and colodess soHd, moderately hygroscopic, saline in taste, and very soluble in water, ammonia, and glycerol. Detailed physical and chemical properties are also available (3,4). 

The resulting nitrous oxide can be recirculated to the nitric acid plant or be used for other purposes. Free acid remaining in the impregnation water of sodium nitrate crystals is neutralized by adding some NaOH to the washing water. Whereas several nitric acid plants utilize absorption of nitrous gases to treat tail gases, almost all of these plants produce small volumes of sodium nitrate. 

In the manufacture of explosives, sodium nitrate is used mainly in blasting agents. In slurries and emulsions, sodium nitrate improves stabiUty and sensitivity. It also improves the energy balance because sodium nitrate replaces water, so that more fuel can be added to the formulation. Sodium nitrate reduces crystal size of slurries, which in turn increases detonating speed. In dynamites sodium nitrate is used as an energy modifier. Typical content of sodium nitrate is 20—50 wt % in dynamites, 5—30 wt % in slurries, and 5—15 wt % in emulsions. Sodium nitrate is used also in permissible dynamites, a special type of dynamite for coal (qv) mining. 

Sodium nitrate is also used in formulations of heat-transfer salts for he at-treatment baths for alloys and metals, mbber vulcanization, and petrochemical industries. A mixture of sodium nitrate and potassium nitrate is used to capture solar energy (qv) to transform it into electrical energy. The potential of sodium nitrate in the field of solar salts depends on the commercial development of this process. Other uses of sodium nitrate include water (qv) treatment, ice melting, adhesives (qv), cleaning compounds, pyrotechnics, curing bacons and meats (see Food additives), organics nitration, certain types of pharmaceutical production, refining of some alloys, recovery of lead, and production of uranium. 

Palladium catalysts have been prepared by fusion of palladium chloride in sodium nitrate to give palladium oxide by reduction of palladium salts by alkaline formaldehyde or sodium formate, by hydrazine and by the reduction of palladium salts with hydrogen.The metal has been prepared in the form of palladium black, and in colloidal form in water containing a protective material, as well as upon supports. The supports commonly used are asbestos, barium carbonate, ... 

A boiler s water may have caustic embrittling characteristics. Only a test using a U.S. Bureau of Mines Embrittlement Detector will show whether this is the case. If the water is found to be embrittling, it is advisable to add sodium nitrate inhibitor lest a weak area of the boiler be attacked. 

Ammonium chloroplatinate often can be used to advantage in place of chloroplatim c acid in the preparation of Adams catalyst. A mixture of 3 g. of ammonium chloroplatinate and 30 g. of sodium nitrate in a casserole or Pyrex beaker is heated gently at first until the rapid evolution of gas slackens and then more strongly until a temperature of 500° is reached. This operation requires about fifteen minutes and there is no spattering. The temperature is held at 500-520° for one-half hour and the mixture is then allowed to cool. The platinum oxide catalyst, collected in the usual way by extracting the soluble salts with water, weighs 1.5 g. and it is comparable in appearance and in activity to the material prepared from chloroplatinic acid. 

Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials No reactions Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Polymerization is accelerated by heat and exposure to oxygen, as well as the presence of contamination such as iron rust. Iron surfaces should be treated with an appropriate reducing agent such as sodium nitrate, before being placed into isoprene service Inhibitor of Polymerization Tertiary butyl catechol (0.06 %). Di-n-butylamine, phenyl-beta-naphthylamine andphenyl-alpha-naphthylamine are also recommended. 

Similar to other types of water treatment, AC filtration is effective for some contaminants and not effective for others. AC filtration does not remove microbes, sodium, nitrates, fluoride, and hardness. Lead and other heavy metals are removed only by a very specific type of AC filter. Unless the manufacturer states that its product will remove heavy metals, one should assume that the AC filter is not effective in removing them. 

For some nonionic, nonpolar polymers, such as polyethylene glycols, normal chromatograms can be obtained by using distilled water. Some more polar nonionic polymers exhibit abnormal peak shapes or minor peaks near the void volume when eluted with distilled water due to ionic interactions between the sample and the charged groups on the resin surface. To eliminate ionic interactions, a neutral salt, such as sodium nitrate or sodium sulfate, is added to the aqueous eluent. Generally, a salt concentration of 0.1-0.5 M is sufficient to overcome undesired ionic interactions. 

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