Lead nitrate oxidant

PbF2 is readily prepared by the action of hydrogen fluoride on lead hydroxide, lead carbonate, or a-lead oxide. It can also be obtained by precipitation from lead nitrate or lead acetate solutions using potassium fluoride, ammonium fluoride, or ammonium bifluoride. 

Nitrates. Iron(II) nitrate hexahydrate [14013-86-6], Fe(N03)2 6H20, is a green crystalline material prepared by dissolving iron in cold nitric acid that has a specific gravity of less than 1.034 g/cm. Use of denser, more concentrated acid leads to oxidation to iron(III). An alternative method of preparation is the reaction of iron(II) sulfate and barium or lead nitrate. The compound is very soluble in water. Crystallisation at temperatures below — 12°C affords an nonahydrate. Iron(II) nitrate is a useful reagent for the synthesis of other iron-containing compounds and is used as a catalyst for reduction reactions. 

Acid Oxidation. Reactions of lead with acid and alkaUes are varied. Nitric acid, the best solvent for lead, forms lead nitrate acetic acid forms soluble lead acetate in the presence of oxygen sulfuric acid forms insoluble lead sulfate. Sulfuric acid is stored in containers with chemical or acid-grade lead. Lead dissolves slowly in HCl, but in the presence of aqueous alkaUes forms soluble plumbites and plumbates. 

Lead borate moaohydrate [14720-53-7] (lead metaborate), Pb(B02)2 H20, mol wt 310.82, d = 5.6g/cm (anhydrous) is a white crystalline powder. The metaborate loses water of crystallization at 160°C and melts at 500°C. It is iasoluble ia water and alkaHes, but readily soluble ia nitric and hot acetic acid. Lead metaborate may be produced by a fusion of boric acid with lead carbonate or litharge. It also may be formed as a precipitate when a concentrated solution of lead nitrate is mixed with an excess of borax. The oxides of lead and boron are miscible and form clear lead-borate glasses in the range of 21 to 73 mol % PbO. 

Another matter of concern in pyrotechnic formulations is the possibiHty of exchange reactions occurring between components. Addition of ammonium salts to compositions containing nitrate oxidizers can produce ammonium nitrate, a very hygroscopic material. The composition then becomes quite prone to pick up water and its performance deteriorates. The addition of an ammonium salt to a chlorate-based formulation can lead to the... 

Bromobenzaldehyde has been prepared by the oxidation of -bromotoluene with chromyl chloride/ by saponification of the acetal from />-bromophenylmagnesium bromide and orthoformic ester/ by the oxidation of ethyl -bromobenzyl ether with nitric acid/ by the oxidation of /j-bromobenzyl bromide with lead nitrate/ and by the hydrolysis of i-bromobenzal bromide in the presence of calcium carbonate. ... 

Gaseous nitrogen dioxide is a brown, paramagnetic, non-flammable, toxic, strongly oxidizing, coiTosive substance shipped in approved, low-pressure steel cylinders. It is prepared in situ by heating lead nitrate ... 

The pollutants most strongly damaging to human, animal, and sometimes plant health include ozone, fine particulate matter, lead, nitrogen oxides (NO ), sulfur oxides (SOJ, and carbon monoxide. Many other chemicals found in polluted air can cause lesser health impacts (such as eye irritation). VOC compounds comprise the bulk of such chemicals. Formaldehyde is one commonly mentioned pollutant of this sort, as is PAN (peroxyacyl nitrate). Such... 

Determination of chromium as lead chromate (precipitation from homogeneous solution) Discussion. Use is made of the homogeneous generation of chromate ion produced by the slow oxidation of chromium(III) by bromate at 90-95 °C in the presence of excess of lead nitrate solution and an acetate buffer. The crystals of lead chromate produced are relatively large and easily filtered the volume of the precipitate is about half that produced by the standard method of precipitation. 

The most recent major expln in a US TNT plant occurred in May 1974 at the Radford Army Ammunition Plant. The accident completely destroyed one of the three continuous nitration lines at the plant. According to the AMC News, Sept 1974, the investigation board reported that an operator inadvertently introduced a 5 to 6-foot rubber hose to clean out unwanted material that had collected in a transfer line leading to the nitrator, when the hose was pulled from his hands into the nitrator. This resulted in a rapid temp rise and subsequent explosion. The hose was commonly used in this manner . The material causing the blockage in the transfer line was believed to be an oxidation product of TNT, 2,2 -dicarboxy-3,3, 5,5,-tetra-nitroazoxybenzene, also referred to as White Compound. The introduction of the rubber hose caused a rapid, exothermic oxidation reaction between the hose material and the mixed acid present. The heat generated by this reaction caused a local acceleration of the normal nitration/oxidation reactions which occur in the nitrator until a critical temp was reached, at which point rapid oxidation of DNT/TNT proceeded as a runaway reaction, igniting the material present in the vessel. 

The sensor s fnnction rests on the property of lead dioxide to sorb nitrogen oxides (NOJ, forming lead nitrate. In this case the lead nitrate concentration is proportional to the nitrogen oxide concentration in the air. The sorption of the nitrogen oxides is a reversible process The Pb02 is regenerated completely within a few minutes when exposed to clean air (free of nitrogen oxides). 

This type of pigment is the precipitate formed when molybdic oxide is dissolved in aqueous sodium hydroxide with the addition of sodium chromate. The resulting mixture is reacted with a solution of lead nitrate. The precipitate formed is further processed through filtration, washing, drying, milling, and packaging. 

Synonym(s) Chromic acid, lead and molybdenum salt lead chromate, sulphate and molybdate molybdenum-lead chromate molybdenum orange Lead dinitrate nitric acid lead(2+) salt lead (II) nitrate plumbous nitrate Lead(2+) oxide lead monoxide litharge massicot Lead(2+) phosphate Phosphoric acid lead(2+) salt ... 

Lead(II) oxide Non-metals Lead(IV) oxide Non-metals Nitric acid Non-metals Nitrogen oxide Non-metals Nitrosyl fluoride Metals, etc. Nitryl fluoride Non-metals Oxygen difluoride Non-metals Potassium nitrite Boron Potassium nitrate Non-metals Silver difluoride Boron, etc. Sodium peroxide Non-metals... 

At physiological pH, ONOO- protonates to peroxynitrous acid (ONOOH) which disappears within a few seconds, the end product being largely nitrate. The chemistry of peroxynitrite/peroxynitrous acid is extremely complex, although addition of ONOO to cells and tissues leads to oxidation and nitration of proteins, DNA and lipids with a reactivity that is comparable to that of hydroxyl radicals. 

Phenylhydrazine Phosgene Phosphine Lead dioxide, oxidizers Aluminum, alkali metals, 2-propanol Air, boron trichloride, bromine, chlorine, nitric acid, nitrogen oxides, nitrous acid, oxygen, silver nitrate... 

Sometimes substances to be determined in gaseous samples are adsorbed on solid adsorbents and then transferred to solution. Thus nitrogen oxides present in the atmosphere are chemisorbed on lead dioxide heated to a temperature of 190 °C. The lead nitrate formed is extracted into hot water and the NO3 anion is then determined [29]. 

Oxidative nitration, a process discovered by Kaplan and Shechter, is probably the most efficient and useful method available for the synthesis of em-dinitroaliphatic compounds from the corresponding nitroalkanes. The process, which is an electron-transfer substitution at saturated carbon, involves treatment of the nitronate salts of primary or secondary nitroalkanes with silver nitrate and an inorganic nitrite in neutral or alkali media. The reaction is believed ° °° to proceed through the addition complex (82) which collapses and leads to oxidative addition of nitrite anion to the nitronate and reduction of silver from Ag+ to Ag . Reactions proceed rapidly in homogeneous solution between 0 and 30 °C. 

Axenrod and co-workers reported a synthesis of TNAZ (18) starting from 3-amino-l,2-propanediol (28). Treatment of (28) with two equivalents of p-toluenesulfonyl chloride in the presence of pyridine yields the ditosylate (29), which on further protection as a TBS derivative, followed by treatment with lithium hydride in THF, induces ring closure to the azetidine (31) in excellent yield. Removal of the TBS protecting group from (31) with acetic acid at elevated temperature is followed by oxidation of the alcohol (32) to the ketone (33). Treatment of the ketone (33) with hydroxylamine hydrochloride in aqueous sodium acetate yields the oxime (34). The synthesis of TNAZ (18) is completed on treatment of the oxime (34) with pure nitric acid in methylene chloride, a reaction leading to oxidation-nitration of the oxime group to em-dinitro functionality and nitrolysis of the A-tosyl bond. This synthesis provides TNAZ in yields of 17-21 % over the seven steps. 

Lead does not evolve hydrogen readily with acids. Nitric acid attacks the metal readily, forming lead nitrate and oxides of nitrogen ... 

The above reaction may be explained by assuming lead tetroxide as formally equivalent to plumbus plumbate having a structure Pb2 [Pbi 04] in which Pb2+ dissolves in dilute nitric acid forming lead(ll) nitrate whde Pb precipitates out as lead(lV) oxide. 

Except silicon, aU other carbon group metals, namely, germanium, tin, and lead, are oxidized by concentrated nitric acid. While germanium and tin form their dioxides, lead forms nitrate. 

Benzoic anhydride has been prepared in rather a poor yield by the action of benzoyl chloride on sodium benzoate,2 barium oxide at 1500,3 benzoic acid at 160-200°,4 sodium nitrite,5 lead nitrate,6 or anhydrous oxalic acid 7 also by treating sodium benzoate with phosphorus pentachloride8 or sulfur chloride.9 More important methods consist in treating benzotrichloride with sulfuric acid,10 and in the action of sodium carbonate upon benzoyl chloride in presence of pyridine.11... 

Compound Name Lead Nitrate Nitric Oxide... 

LEAD NITRATE Nitric Acid, Lead II salt Oxidizing Material, II 1 0 0 oxy... 

Lead Nitrate — Fire Hazards Flash Point (deg. F) Not flammable Flammable Limits in Air (%) Not flammable Fire Extinguishing Agents Not pertinent Fire Extinguishing Agents Not To Be Used Not pertinent Special Hazards of Combustion Products Toxic oxides of nitrogen may form in fire ... 

Lead nitrate (Pb[N03]2) Heavy metal oxidizer used in slow explosive compositions (Plumbatol)... 

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