Chromium complexes oxidation catalysts

At present, the main industrial catalyst of ammonia oxidation is platinum and its alloys with aluminium and rhodium. Taking into account the deficit and high cost of platinum metals, the dcCTcasing of the consumption and losses of platinum metals is an urgent problem. Therefore, several compositions of complex oxide catalysts have been developed with iron (111), cobalt and chromium oxides as an active component. Complex oxides with perovskite structure are used as new catalysts they provide selective oxidation of ammonia with an yield not less than 90 %. The authors of [33] proposed to use perovskite powders LaMeOj, where Me=Fe, Co, Ni, Cr, Mn, and La,.,Sr,Me03, where Me=Co, Mn and x=0.25-0.75. To prepare these compounds, they used the precipitation by tetraethyl ammonia from diluted nitrate solutions taken at necessary ratios. The powders as prepared are poorly molded as in the form of honeycomb stractures as well as in the form of simple granules. 

The interpretation of data on the change of Kp as a result of the reduction treatment of the chromium oxide catalyst (97) is hindered by the absence of precise data on the composition of the surface complexes being formed. 

Table IV presents the results of the determination of polyethylene radioactivity after the decomposition of the active bonds in one-component catalysts by methanol, labeled in different positions. In the case of TiCU (169) and the catalyst Cr -CjHsU/SiCU (8, 140) in the initial state the insertion of tritium of the alcohol hydroxyl group into the polymer corresponds to the expected polarization of the metal-carbon bond determined by the difference in electronegativity of these elements. The decomposition of active bonds in this case seems to follow the scheme (25) (see Section V). But in the case of the chromium oxide catalyst and the catalyst obtained by hydrogen reduction of the supported chromium ir-allyl complexes (ir-allyl ligands being removed from the active center) (140) C14 of the...

A second manufacturing method for acetic acid utilizes butane from the C4 petroleum stream rather than ethylene. It is a very complex oxidation with a variety of products formed, but conditions can be controlled to allow a large percentage of acetic acid to be formed. Cobalt (best), manganese, or chromium acetates are catalysts with temperatures of 50-250 °C and a pressure of 800 psi. 

Chromyl chloride is used in many organic synthetic reactions including oxidation and chlorination. It also is used as a catalyst in olefin polymerization in the preparation of chromium complexes and as a solvent for chromic anhydride. 

The supported chromium complex "CHRISS" was first reported by us in 1997 (Figure 6) [10]. It was shown to be stable to reaction conditions and an active catalyst for the oxidation of methylaromatics with air as the only consumable source of oxygen. The catalyst was prepared by first forming in solution a metal complex with pendant triethoxysilane groups which is then imprinted onto a silica gel surface. 

The kinetics of chromium(l 11 )-catalyscd oxidation of fonnic acid by Ce(TV) in aqueous H2SO4 can be rationalized in terms of initial formation of an outer-sphere complex involving oxidant, catalyst, and substrate (S), Ce(TV)(S)Cr(III), followed by an inner-sphere complex Ce(III)(S)Cr(IV). It is proposed that electron transfer occurs within this complex from substrate to Cr(TV) (with elimination of H+) followed by fast reaction to give CO2 (again with elimination of H+).54 In contrast, there was no kinetic evidence for the accumulation of a corresponding inner-sphere intermediate in the osmium(VIII)-catalysed Ce(TV) oxidation of DMSO to dimethyl sulfone here, the observed rate law was rationalized in terms of rate-determining bimolecular electron transfer from DMSO to Os(VHI) in an outer-sphere step.55 The kinetics of oxidation of 2-hydroxy-l-naphthalidene anil by cerium(IV) in aqueous sulfuric acid have been... 

Polymerization with Complex Catalysts. High density polyethylene reached a domestic production of 1.25 billion pounds in 1968. It is made either with a stereospecific Ziegler-Natta catalyst or on a supported chromium oxide catalyst. The latter forms a complex with the silica-alumina and is activated by treatment with air and steam at elevated temperature. The mechanism is such that electrons are donated to the catalyst in order to be returned under polymerizational-promoting conditions, consequently lowering the energy of the system ... 

The idea that complex formation may be important in the catalytic process can be carried further. It has been found, for example, that bis-arene chromium complexes supported on silica-alumina are active for ethylene polymerization. These catalysts are prepared by activating the support alone in the usual manner and then impregnating with a hydrocarbon solution of the bis-arene compound at room temperature in the absence of air or other oxidizing agent. 

Complex oxides of the perovskite structure containing rare earths like lanthanum have proved effective for oxidation of CO and hydrocarbons and for the decomposition of nitrogen oxides. These catalysts are cheaper alternatives than noble metals like platinum and rhodium which are used in automotive catalytic converters. The most effective catalysts are systems of the type Lai vSrvM03, where M = cobalt, manganese, iron, chromium, copper. Further, perovskites used as active phases in catalytic converters have to be stabilized on the rare earth containing washcoat layers. This then leads to an increase in rare earth content of a catalytic converter unit by factors up to ten compared to the three way catalyst. 

Bisbenzene chromium has been found to be a catalyst for the polymerization of ethylene at 200°-250°C. Chromium metal was postulated as the active catalyst in the system 410, 411). The polymerization of ethylene by bisarene chromium(I) salts in the presence of (i-Bu)3Al has also been studied (406). The catalytic activity was found to be a function of both the arene and the anion present. When bisarene chromium complexes are air oxidized in water, hydrogen peroxide is produced ... 

Use Organic oxidations and chlorinations, solvent for chromic anhydride, chromium complexes and dyes, catalyst. 

One other notable method has been used in the preparation of mixed transition metal molybdates, amongst many other oxide systems. This novel method(TT) involves preparation of the mixed metal oxides via an amorphous precursor such as a citrate salt of the appropriate metals, and then thermal decomposition of the complex to yield the resulting mixed oxides. The experimental procedures are described in four French patents(78-81), giving details of many different preparations including a proposed M0O3 rich, chromium doped iron molybdate, prepared as a possible selective oxidation catalyst. 

---