Sodium magnesium alloys

In addition to freshwater, seawater is also a source for sodium, magnesium, chlorides, iodine, bromine, and magnesium metal (see Sodium coLD>ouNDS Magnesium coLD>ouNDS Iodine Bromine Magnesiumand magnesium alloys). Many other elements are certain to be economically obtained from the ocean as technology for the recovery improves. 

Mixtures of the red or yellow oxides with sodium-potassium alloy explode violently on impact, the yellow (more finely particulate) oxide giving the more sensitive mixture [1], Mixtures with magnesium or potassium may explode on heating [2],... 

Individually indexed alloys or intermetallic compounds are Aluminium amalgam, 0051 Aluminium-copper-zinc alloy, 0050 Aluminium-lanthanum-nickel alloy, 0080 Aluminium-lithium alloy, 0052 Aluminium-magnesium alloy, 0053 Aluminium-nickel alloys, 0055 Aluminium-titanium alloys, 0056 Copper-zinc alloys, 4268 Ferromanganese, 4389 Ferrotitanium, 4391 Lanthanum-nickel alloy, 4678 Lead-tin alloys, 4883 Lead-zirconium alloys, 4884 Lithium-magnesium alloy, 4681 Lithium-tin alloys, 4682 Plutonium bismuthide, 0231 Potassium antimonide, 4673 Potassium-sodium alloy, 4646 Silicon-zirconium alloys, 4910... 

The bimolecular reduction of aromatic nitro compounds, depending on reaction conditions, may produce azoxy compounds, azo compounds, hydrazo compounds (1,2-diarylhydrazines), benzidines, or amines. Whereas the reduction with zinc and sodium hydroxide leads to azo compounds, zinc and acetic acid/acetic anhydride produces azoxy compounds. Other reducing agents suggested are stannous chloride, magnesium with anhydrous methanol, a sodium-lead alloy in ethanol, thallium in ethanol, and sodium arsenite. 

Activity in this area has stemmed from the discovery that reduction of MX5 or their complexes to yield molecular MUI trihalide adducts can be achieved rather easily by using reductants such as sodium amalgam, sodium-potassium alloy and magnesium in the presence of ligands. 

Potassium, sodium, magnesium, and mercury can be distilled over niobium without formation of alloys arsenic, antimony, and tellurium do not form alloys below 500° to 600° C. 

Lead—tin alloys, 4877 Lead—zirconium alloys, 4878 Lithium—magnesium alloy, 4676 Lithium—tin alloys, 4677 Plutonium bismuthide, 0231 Potassium antimonide, 4668 Potassium—sodium alloy, 4641 Silicon—zirconium alloys, 4904 Silver—aluminium alloy, 0002 Silvered copper, 0003 Sodium germanide, 4412 Sodium—antimony alloy, 4791 Sodium—zinc alloy, 4792 Titanium—zirconium alloys, 4915... 

Sacrificial anode — is a piece of metal used as an anode in electrochemical processes where it is intended to be dissolved during the process. In -+ corrosion protection it is a piece of a non-noble metal or metal alloy (e.g., magnesium, aluminum, zinc) attached to the metal to be protected. Because of their relative -+ electrode potentials the latter is established as the -+ cathode und thus immune to corrosion. In -+ electroplating the metal used as anode may serve as a source for replenishing the electrolyte which is consumed by cathodic deposition. The sodium-lead alloy anode used in the electrochemical production of tetraethyl lead may also be considered as a sacrificial anode. 

In 1954, van der Kerk and Luijten found that in the direct synthesis of tetraorganyl-stannanes the tin — sodium alloy can be replaced with a tin-magnesium alloy . A mercury catalyst (Hg or HgCl2) was required for this variant and the process was conducted at 160 °C under pressure. 

The reactivities of alkyl halides are in the sequence RI > RBr > RCl and MeX > EtX > PrX. Benzyl hahde reactions with tin do not require catalysts (equation 2). For less reactive halides, the catalysts and promoters employed include metals (sodium, magnesium, zinc, or copper), Lewis bases (amines, triorganophosphines and -stibines, alcohols, or ethers), iodides, and onium salts (R4MX). The use of tin-sodimn alloys can result in tri- or tetraorganotin products. Electrochemical synthesis has also been reported, e.g. the formation of R2SnX2 from the oxidation of anodic tin by RX in benzene solution and the formation of ILtSn from RI (R = Me or NCCH2CH2) and cathodic tin. 

Strontium nitrate Dextrin Red gum Polyvinyl chloride White sparks aluminum, magnesium, aluminum-magnesium alloy, titanium Whistle effect potassium benzoate or sodium salicylate White smoke mixture of potassium nitrate and sulfur Colored smoke mixture of potassium chlorate, sulfur, and an organic dye... 

Flammable gas. Very dangerous fire hazard when exposed to heat, flame, or powerful oxidizers. Moderate explosion hazard when exposed to flame and sparks. Explodes on contact with interhalogens (e.g., bromine trifluoride, bromine pentafluoride), magnesium and alloys, potassium and alloys, sodium and alloys, zinc, Potentially explosive reaction with aluminum when heated to 152° in a sealed container. Mixtures with aluminum chloride + ethylene react exothermically and then explode when pressurized to above 30 bar. May ignite on contact with aluminum chloride or powdered aluminum. To fight fire, stop flow of gas and use CO2, dry chemical, or water spray. When heated to decomposition it emits highly toxic fumes of cr. See also CHLORINATED HYDROCARBONS, ALIPHATIC. 

Mbtalation Benzyllithium. Naphthalene-Magnesium. Naphthalene-Sodium. Phenylpotassium. Sodium amalgam. Sodium-Potassium alloy. 

Met-L-X [Ansul]. TM for a dry chemical based on sodium chloride, approved for use on sodium, potassium, sodium-potassium alloy, and magnesium fires. 

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