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Boric acid magnesium

Aluminum sulfate Salts Copper sulfate Boric acid Magnesium sulfate... [Pg.160]

Boron (Buraq in Arabic/Burah in Persian, which is the word for white, the color being attributed to borax (sodium tetraborate, Na2B4O7.10H2O)) was discovered in 1808 independently by the British Chemist, Sir Humphry Davy, and two French chemists, Joseph Louis Gay-Lussac and Loius Jacques Thenard.1 They isolated boron in 50% purity by the reduction of boric acid with sodium or magnesium. The Swedish chemist Jons Jakob Berzilius identified boron as an element in 1824. The first pine sample of boron was produced by the American chemist William Weintraub in 1909. Boron does not appear in nature in elemental form, but is found in its compounded... [Pg.19]

Boron itself was first produced in 1808 by Sir Humphrey Davy, who carried out the electrolysis of molten boric acid. The reduction of boric acid by potassium was used as a preparative method by Gay-Lussac and Thenard in 1808, and reduction of B203 by magnesium was the method used by Moissan in 1895. [Pg.423]

Preparation. It is difficult to prepare very pure boron. The element can be obtained by magnesium reduction of the oxide, B203. The oxide is made by melting boric acid which in turn is obtained from borax. [Pg.480]

Procedure. Steam is passed through the steam distillation apparatus for 20-30 min. Check the performance by pipetting 5 ml ammonium-N standard solution into the distillation unit, add 1 drop octan-2-ol, 6 ml magnesium hydroxide suspension and steam distil the released ammonia into 5 ml boric acid solution in a 100-ml conical flask. After approximately 40 ml distillate has been collected over a 5-min period, wash the tip of the condenser into the distillate, add 2-3 drops mixed indicator solution and titrate with 0.005 M H SO until the colour changes from green to purple. A blank distillation/titra-tion is carried out using 5 ml ammonia-free water and subtracted from the standard titre to give a result which should be 5.00 ml. [Pg.65]

Magnesium is a very reactive metal and makes an excellent fuel under the proper conditions. It is oxidized by moist air to form magnesium hydroxide, Mg(OH) 2, and it readily reaets with all acids, including weak species such as vinegar (5% acetic acid) and boric acid. The reactions of magnesium with water and an acid (HX) are shown below ... [Pg.42]

These masses contained boric acid, ammonium borate, sulfates of iron and calcium, and (occasionally) magnesium sulfate. [Pg.582]

Uses Of the Stassfurt salts.—The magnesium compounds in the Stassfurt salts are used for the preparation of magnesium and of its salts. The potash salts are an essential constituent of many fertilizers used in agriculture, etc. 22 and potassium chloride is the starting-point for the manufacture of the many different kinds of potassium salts used in commerce—carbonate, hydroxide, nitrate, chlorate, chromate, alum, ferrocyanide, cyanide, iodide, bromide, etc. Chlorine and bromine are extracted by electrolysis and other processes from the mother liquids obtained in the purification of the potash salts. Boric acid and borax are prepared from boracite. Caesium and rubidium are recovered from the crude carnallite and sylvite. [Pg.435]

Preparation of Amorphous Boron from Boric Acid Anhydride. (Each student performs only one of the experiments for preparing amorphous boron.) Put 2 g of boric acid anhydride into an iron crucible or onto an iron plate and roast it if the boric acid anhydride contains moisture, then when it is heated with magnesium an explosion may occur ). Triturate the boric acid anhydride as rapidly as possible (why ) in 4 mortar, weigh 1 g and mix it with 2 g of a magnesium powder. Place the mixture into a refractory test tube and fasten it in an inclined position in a clamp of a stand in a fume cupboard . First carefully heat the test tube with the mixture with the flame of a burner, and then strongly heat the bottom part of the tube. What do you observe ... [Pg.176]

When aldehydes, with or without a hydrogen, are treated with aluminum ethoxide, one molecule is oxidized and another reduced, as in 9-69, but here they are found as the ester. The process is called the Tishchenko reaction. Crossed Tishchenko reactions are also possible. With more strongly basic alkoxides, such as magnesium or sodium alkoxides, aldehydes with an a hydrogen give the aldol reaction. Like 9-69, this reaction has a mechanism that involves hydride transfer.751 The Tishchenko reaction can also be catalyzed752 by ruthenium complexes.753 by boric acid,754 and, for aromatic aldehydes, by disodium tetracarbonylferrate Na2Fe(CO)4,755 OS I, 104. [Pg.1235]

It has likewise been shown by Morozov [30] that it is possible to coagulate nitrocellulose under the influence of boric acid, in the presence of the following metal oxides Mn, Fe, Ni, Cu, and Zn. This author noticed that the nitrocotton gel formed owing to the influence of the oxides redissolved in the course of time, probably as a result of a change in chemical composition. On the other hand, the precipitate obtained by treating nitrocellulose with plumbous oxide or aluminium oxide is insoluble. Papkov and Khveleva [31] have established that a similar coagulation takes place under the influence of such salts as zinc sulphate, magnesium chloride and aluminium chloride. [Pg.302]

Antiseptic -boric acid as [BORON COMPOUNDS - BORON OXIDES, BORIC ACID AND BORATES] (Vol 4) -isopropyl alcohol as [PROPYL ALCOHOLS - ISOPROPYL ALCOHOL] (Vol 20) -magnesium acetate as (MAGNESIUM COMPOUNDS] (Vol 15) -organobrommes as [BROMINE COMPOUNDS] (Vol 4)... [Pg.65]

Fuel additives - [AMNES-CYCLOALIPHATIC AMINES] (Vol 2) - [SULFONIC ACIDS] (Vol 23) -arsenic compds as [ARSENIC COMPOUNDS] (Vol 3) -boron compds as [BORON COMPOUNDS - BORIC ACID ESTERS] (Vol 4) -coordination compounds as [COORDINATION COMPOUNDS] (Vol 7) -ethers m [ETHERS] (Vol 9) -magnesium alkyls as [MAGNESIUM COMPOUNDS] (Vol 15) -polyamines as [DIAMINES AND HIGHER AMINES ALIPHATIC] (Vol 8) -htanates as [TITANIUM COMPOUNDS - ORGANIC] (Vol 24) -use of copper compounds [COPPER COMPOUNDS] (Vol 7)... [Pg.425]

The effect of neutral salts (e.g., NaCl) on the composition of borates precipitated from, or in equilibrium with, aqueous solutions doubtless arises from a reduction in water activity, metal borate complexation, and a shift in polyborate equilibria (Sections IV,A, B). The "indifferent or inert component method has frequently been used for the synthesis of borates. Potassium and sodium chlorides can be used to enhance the precipitation of specific nickel (48), aluminum (51), iron (49), and magnesium (151) borates. In the K20-B203-H20 system at 25°C (248), the presence of potassium chloride results in a reduced boric acid crystallization curve, lower borate solubilities, lower pH, and an extended B203 K20 range over which the pentaborate crystallizes. [Pg.210]


See other pages where Boric acid magnesium is mentioned: [Pg.457]    [Pg.110]    [Pg.478]    [Pg.457]    [Pg.110]    [Pg.478]    [Pg.331]    [Pg.347]    [Pg.273]    [Pg.148]    [Pg.184]    [Pg.298]    [Pg.215]    [Pg.1548]    [Pg.273]    [Pg.209]    [Pg.80]    [Pg.274]    [Pg.274]    [Pg.148]    [Pg.184]    [Pg.248]    [Pg.160]    [Pg.466]    [Pg.183]    [Pg.289]    [Pg.403]    [Pg.447]    [Pg.770]    [Pg.825]    [Pg.845]    [Pg.23]    [Pg.208]    [Pg.208]    [Pg.212]    [Pg.773]   


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Acids magnesium

Boric acid

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