Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sodium hydroxide, molten

Assemble the apparatus shown in Fig. 1 V, 67, 1 this is self-explanatory. The distilling flask has a capacity of 250 ml. and the beaker contains 150 ml. of 10 per cent, sodium hydroxide solution. All corks must fit well and should be coated with paraflSn wax (by dipping into molten wax, and allowing to drain). Place half of the yield of the dry phenyldiazonium fluoborate in the distilling flask. Heat the solid gently with a small luminous flame at one point near its surface until decomposition begins withdraw the flame and allow the reaction to continue... [Pg.610]

Chemica.1 Properties. The FEP resin is inert to most chemicals and solvents, even at elevated temperatures and pressures. However, it reacts with fluorine, molten alkah metal, and molten sodium hydroxide. Acids or bases are not absorbed at 200°C and exposures of one year. The absorption of organic solvents is less than 1% at elevated temperatures and long exposure times. Absorption of chemicals or solvents has no effect on the chemical integrity of the FEP molecule and is a reversible physical process. [Pg.361]

Naphthalenediol. This diol is made by the fusion of sodium 2,7-naphthalenedisulfonate with molten sodium hydroxide at 280—300°C in ca 80% yield. A formaldehyde resin prepared from this diol has excellent erosion resistance, strength, and chemical inertness it is used as an ablative material in rocket-exhaust environments (76). [Pg.500]

In the alkaline process, an aqueous solution of sodium hydroxide is allowed to react with molten, yellow phosphoms. A long-chain alcohol is used as a dispersant (3). The reaction to produce phosphine may be represented by equation 1. [Pg.317]

Gas-phase oxidation of propylene using oxygen in the presence of a molten nitrate salt such as sodium nitrate, potassium nitrate, or lithium nitrate and a co-catalyst such as sodium hydroxide results in propylene oxide selectivities greater than 50%. The principal by-products are acetaldehyde, carbon monoxide, carbon dioxide, and acrolein (206—207). This same catalyst system oxidizes propane to propylene oxide and a host of other by-products (208). [Pg.141]

If tin and sulfur are heated, a vigorous reaction takes place with the formation of tin sulfides. At 100—400°C, hydrogen sulfide reacts with tin, forming stannous sulfide however, at ordinary temperatures no reaction occurs. Stannous sulfide also forms from the reaction of tin with an aqueous solution of sulfur dioxide. Molten tin reacts with phosphoms, forming a phosphide. Aqueous solutions of the hydroxides and carbonates of sodium and potassium, especially when warm, attack tin. Stannates are produced by the action of strong sodium hydroxide and potassium hydroxide solutions on tin. Oxidizing agents, eg, sodium or potassium nitrate or nitrite, are used to prevent the formation of stannites and to promote the reactions. [Pg.64]

Zirconium is not attacked by caustics up to boiling temperatures. It is resistant to molten sodium hydroxide to 1000°C, but is less resistant to potassium hydroxide. [Pg.429]

CP can also be prepared by the reaction of cellulose with phosphoms oxychloride in pyridine (37) or ether in the presence of sodium hydroxide (38). For the most part these methods yield insoluble, cross-linked, CP with a low DS. A newer method based on reaction of cellulose with molten urea—H PO is claimed to give water soluble CP (39). The action of H PO and P2 5 cellulose in an alcohol diluent gives a stable, water-soluble CP with a high DS (>5% P) (40). These esters are dame resistant and have viscosities up to 6000 mPa-s(=cP) in 5 wt % solution. Cellulose dissolved in mixtures of DMF—N2O4 can be treated with PCl to give cellulose phosphite [37264-91-8] (41) containing 11.5% P and only 0.8% Cl. Cellulose phosphinate [67357-37-5] and cellulose phosphonate [37264-91 -8] h.a.ve been prepared (42). [Pg.265]

Reaction of benzenesulfonic acid with sodium hydroxide This is the oldest method for the preparation of phenol. Benzene is sulfonated and the benzenesulfonic acid heated with molten sodium hydroxide. Acidification of the reaction mixture gives phenol. [Pg.1000]

The equilibrium of metals with molten sodium hydroxide and with fused alkali chlorides " has been studied in detail. Williams, Grand and Miller studied the reaction of molten sodium hydroxide with nickel. [Pg.437]

The electrolyte salt must be processed to recover the ionic plutonium orginally added to the cell. This can be done by aqueous chemistry, typically by dissolution in a dilute sodium hydroxide solution with recovery of the contained plutonium as Pu(OH)3, or by pyrochemical techniques. The usual pyrochemical method is to contact the molten electrolyte salt with molten calcium, thereby reducing any PUCI3 to plutonium metal which is immiscible in the salt phase. The extraction crucible is maintained above the melting point of the contained salts to permit any fine droplets of plutonium in the salt to coalesce with the pool of metal formed beneath the salt phase. If the original ER electrolyte salt was eutectic NaCl-KCl a third "black salt" phase will be formed between the stripped electrolyte salt and the solidified metal button. This dark-blue phase can contain 10 wt. % of the plutonium originally present in the electrolyte salt plutonium in this phase can be recovered by an additional calcium extraction stepO ). [Pg.401]

It is also attacked by the Lewis base OH in hot, molten sodium hydroxide and by O2- from the carbonate anion of hot molten sodium carbonate ... [Pg.736]

The formation of ad-quinonoid transient intermediates by electronic excitation has been identified spectroscopically. Proton abstractors (bases) such as sodium hydroxide, potassium iodide or tetramethylammonium octahydrotriborate induce deflagration in molten TNT. [Pg.883]

While drying hydrazine over sodium hydroxide pellets, explosive decomposition occurred, spraying molten sodium hydroxide around. This was attributed to possible leakage of air into the evacuated flask. [Pg.1677]

Sodium chloride is found in salt beds, salt brines, and sea water throughout the world, and it is also mined is some locations. Consequently, sodium chloride is the source of numerous other sodium compounds. A large portion of the sodium chloride utilized is consumed in the production of sodium hydroxide (Eq. (11.23)). The production of sodium metal involves the electrolysis of the molten chloride, usually in the form of a eutectic mixture with calcium chloride. Sodium carbonate is an important material that is used in many ways such as making glass. It was formerly produced from NaCl by means of the Solvay process, in which the overall reaction is... [Pg.364]

At high temperature, arsenic dissolves in molten sodium hydroxide with the liberation of hydrogen. Write the equation for the reaction. [Pg.520]

Gravimelt A coal cleaning process in which coal is heated with molten sodium hydroxide and then washed with acid. The process removes 90 percent of the sulfur and 95 percent of the ash. It was planned to be piloted in 1987. [Pg.117]

Harris A softening process for removing antimony, arsenic, and tin from lead. The mixed metals are heated with a molten mixture of sodium hydroxide and sodium nitrate. Invented by H. Harris at H. J. Enthoven Sons. [Pg.124]

The primary starting material for the synthesis of perylene tetracarboxylic acid pigments is the dianhydride 71. It is prepared by fusing 1,8-naphthalene dicar-boxylic acid imide (naphthalic acid imide 69) with caustic alkali, for instance in sodium hydroxide/potassium hydroxide/sodium acetate at 190 to 220°C, followed by air oxidation of the molten reaction mixture or of the aqueous hydrolysate. The reaction initially affords the bisimide (peryldiimide) 70, which is subsequently hydrolyzed with concentrated sulfuric acid at 220°C to form the dianhydride ... [Pg.474]

The causes of furnace blasts occurring in soda-regeneration plants when water is spilt into molten sodium carbonate, sodium chloride, sodium hydroxide, sodium sulfate or sodium sulfide are discussed, together with methods of prevention. [Pg.263]

In 1807 Sir Humphry Davy (1778-1829) devised an electrolysis apparatus that used electrodes immersed in a bath of melted sodium hydroxide. When he passed an electric current through the system, metallic sodium formed at the negative (cathode) electrode. He first performed this experiment with molten potassium carbonate to liberate the metal potassium, and he soon followed up with the sodium experiment. Today, sodium and some of the other alkali metals are still produced by electrolysis. The types of electrolytes may vary using a mixture of sodium chloride and calcium chloride and then further purifying the sodium metal. [Pg.51]

Benzene is sulphonated with oleum and benzene sulphonic acid so formed is converted to sodium phenoxide on heating with molten sodium hydroxide. Acidification of the sodium salt gives phenol. [Pg.55]


See other pages where Sodium hydroxide, molten is mentioned: [Pg.918]    [Pg.951]    [Pg.918]    [Pg.951]    [Pg.245]    [Pg.250]    [Pg.354]    [Pg.667]    [Pg.970]    [Pg.352]    [Pg.277]    [Pg.169]    [Pg.199]    [Pg.130]    [Pg.609]    [Pg.917]    [Pg.298]    [Pg.489]    [Pg.667]    [Pg.970]    [Pg.20]    [Pg.321]    [Pg.305]    [Pg.271]    [Pg.347]   
See also in sourсe #XX -- [ Pg.2 , Pg.132 , Pg.134 ]

See also in sourсe #XX -- [ Pg.2 , Pg.132 , Pg.134 ]




SEARCH



Hydroxides Sodium hydroxide

Hydroxides, molten

Molten sodium

Sodium hydroxide

© 2024 chempedia.info