Nickel oxide reaction with

Nickel oxide anodes are another example for a relatively simple oxide electrocatalyst used rather widely in the oxidation of organic substances (alcohols, amines, etc.) in alkaline solutions at relatively low anodic potentials (about +0.6 V RHE). These processes, which occur at an oxidized nickel surface, are rather highly selective. As an example, we mention the industrial oxidation of diacetone-L-sorbose to the corresponding acid in vitamin C synthesis. This reaction occurs at nickel oxide electrodes with chemical yields close to 100%. 

Raney-nickel catalysts are barely sensitive to catalyst poisoning (as are Pt-activated cathodes), e.g., by iron deposition, but they deteriorate due to loss of active inner surface because of slow recrystallization—which unavoidably leads to surface losses of 50% and more over a period of 2 years. A further loss mechanism is oxidation of the highly dispersed, reactive Raney nickel by reaction with water (Ni + 2H20 — Ni(OH)2 + 02) under depolarized condition, that is, during off times in contact with the hot electrolyte after complete release of the hydrogen stored in the pores by diffusion of the dissolved gas into the electrolyte. 

By reducing hydrated nickel(II) nitrate with NaBHt, in the presence of the tetradentate tripodal ligand np3 (equation 80), the complex [Ni(np3)j (66) has been obtained.263 Complex (66) undergoes oxidative reaction with HC104 or HBF4 to afford the nickel(II) hydrido complex [NiH ps)]-1".264 It also reacts with CO to give the carbonyl derivative263 and with white... 

Konaka, R.,Terabe, S., and Kuruma. K. 1969. Mechanism of the oxidation reaction with nickel peroxide. Journal of Organic Chemistry 34, 1334-1337. 

McBreen comprehensively reviewed nickel hydroxide battery electrodes, the solid state chemistry of nickel hydroxides, and the electrochemical reactions of the Ni(OH)21 NiOOH couple. Any critical discussion of the thermodynamic data of nickel oxide hydroxides with higher oxidation states has to refer to this splendidly written account of nickel solid state electrochemistry. 

Al) aimed to reduce the Co content, and stabilize the structure to reversible lithium extraction. Materials with high nickel content LiNii j,M M j,02 are appealing, but suffer from oxidation reactions with the electrolyte at elevated temperature/voltage as does LiNi02. Band structure considerations indicate that extraction of oxygen from the lattice competes with removal of Li+ at high potential, in the order Ni > Co > Mn. ... 

With regard to Eq. (9-20) a steady state coverage with NiO(OH) will be attained, i.e. continuous oxidation reaction with a continuous current flow will be observed under potentiostatic conditions. All this means that the nickel oxide catalyst is turned into a nickel oxide electrocatalyst, that can be used in electrosynthesis. The most important synthetic reactions emplo)dng such electrodes are as follows ... 

Reactions with Ammonia and Amines. Acetaldehyde readily adds ammonia to form acetaldehyde—ammonia. Diethyl amine [109-87-7] is obtained when acetaldehyde is added to a saturated aqueous or alcohoHc solution of ammonia and the mixture is heated to 50—75°C in the presence of a nickel catalyst and hydrogen at 1.2 MPa (12 atm). Pyridine [110-86-1] and pyridine derivatives are made from paraldehyde and aqueous ammonia in the presence of a catalyst at elevated temperatures (62) acetaldehyde may also be used but the yields of pyridine are generally lower than when paraldehyde is the starting material. The vapor-phase reaction of formaldehyde, acetaldehyde, and ammonia at 360°C over oxide catalyst was studied a 49% yield of pyridine and picolines was obtained using an activated siHca—alumina catalyst (63). Brown polymers result when acetaldehyde reacts with ammonia or amines at a pH of 6—7 and temperature of 3—25°C (64). Primary amines and acetaldehyde condense to give Schiff bases CH2CH=NR. The Schiff base reverts to the starting materials in the presence of acids. 

Na.tura.1 Ga.s Reforma.tion. In the United States, most hydrogen is presently produced by natural gas reformation or methane—steam reforming. In this process, methane mixed with steam is typically passed over a nickel oxide catalyst at an elevated temperature. The reforming reaction is... 

Nickel Carbonyl The extremely toxic gas nickel carbonyl can be detected at 0.01 ppb by measuring its chemiluminescent reaction with ozone in the presence of carbon monoxide. The reaction produces excited nickel(II) oxide by a chain process which generates many photons from each pollutant molecule to permit high sensitivity (315). 

In the acid-leaching process, the oxide ore is leached with sulfuric acid at elevated temperature and pressure, which causes nickel, but not iron, to enter into solution. The leach solution is purified, foHowed by reaction with hydrogen sulfide and subsequent precipitation of nickel and cobalt sulfides. 

Nickel chloride hexahydrate [7791-20-0] is formed by the reaction of nickel powder or nickel oxide with a hot mixture of water and HCl. Nickel duoride [13940-83-5], 4H2O, is prepared by the reaction of hydroduoric acid on nickel carbonate. Nickel bromide [18721 -96-5], NiBr2 6H20, is made... 

Nickel Sulfamate. Nickel sulfamate [13770-89-3] Ni(S02NH2)2 4H2O, commonly is used as an electrolyte ia nickel electroforming systems, where low stress deposits are required. As a crystalline entity for commercial purposes, nickel sulfamate never is isolated from its reaction mixture. It is prepared by the reaction of fine nickel powder or black nickel oxide with sulfamic acid ia hot water solution. Care must be exercised ia its preparation, and the reaction should be completed rapidly because sulfamic acid hydrolyzes readily to form sulfuric acid (57). 

The zwitterion (6) can react with protic solvents to produce a variety of products. Reaction with water yields a transient hydroperoxy alcohol (10) that can dehydrate to a carboxyUc acid or spHt out H2O2 to form a carbonyl compound (aldehyde or ketone, R2CO). In alcohoHc media, the product is an isolable hydroperoxy ether (11) that can be hydrolyzed or reduced (with (CH O) or (CH2)2S) to a carbonyl compound. Reductive amination of (11) over Raney nickel produces amides and amines (64). Reaction of the zwitterion with a carboxyUc acid to form a hydroperoxy ester (12) is commercially important because it can be oxidized to other acids, RCOOH and R COOH. Reaction of zwitterion with HCN produces a-hydroxy nitriles that can be hydrolyzed to a-hydroxy carboxyUc acids. Carboxylates are obtained with H2O2/OH (65). The zwitterion can be reduced during the course of the reaction by tetracyanoethylene to produce its epoxide (66). 

Dehalogenation of monochlorotoluenes can be readily effected with hydrogen and noble metal catalysts (34). Conversion of -chlorotoluene to Ncyanotoluene is accompHshed by reaction with tetraethyl ammonium cyanide and zero-valent Group (VIII) metal complexes, such as those of nickel or palladium (35). The reaction proceeds by initial oxidative addition of the aryl haHde to the zerovalent metal complex, followed by attack of cyanide ion on the metal and reductive elimination of the aryl cyanide. Methylstyrene is prepared from -chlorotoluene by a vinylation reaction using ethylene as the reagent and a catalyst derived from zinc, a triarylphosphine, and a nickel salt (36). 

Lateritic Ores. The process used at the Nicaro plant in Cuba requires that the dried ore be roasted in a reducing atmosphere of carbon monoxide at 760°C for 90 minutes. The reduced ore is cooled and discharged into an ammoniacal leaching solution. Nickel and cobalt are held in solution until the soflds are precipitated. The solution is then thickened, filtered, and steam heated to eliminate the ammonia. Nickel and cobalt are precipitated from solution as carbonates and sulfates. This method (8) has several disadvantages (/) a relatively high reduction temperature and a long reaction time (2) formation of nickel oxides (J) a low recovery of nickel and the contamination of nickel with cobalt and (4) low cobalt recovery. Modifications to this process have been proposed but all include the undesirable high 760°C reduction temperature (9). 

Nickel peroxide is a solid, insoluble oxidant prepared by reaction of nickel (II) salts with hypochlorite or ozone in aqueous alkaline solution. This reagent when used in nonpolar medium is similar to, but more reactive than, activated manganese dioxide in selectively oxidizing allylic or acetylenic alcohols. It also reacts rapidly with amines, phenols, hydrazones and sulfides so that selective oxidation of allylic alcohols in the presence of these functionalities may not be possible. In basic media the oxidizing power of nickel peroxide is increased and saturated primary alcohols can be oxidized directly to carboxylic acids. In the presence of ammonia at —20°, primary allylic alcohols give amides while at elevated temperatures nitriles are formed. At elevated temperatures efficient cleavage of a-glycols, a-ketols... 

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