Light partial oxidation

Other apphcations of sodium bromide iaclude use ia the photographic iadustry both to make light-sensitive silver bromide [7785-23-1] emulsions and to lower the solubiUty of silver bromides during the developing process use as a wood (qv) preservative in conjunction with hydrogen peroxide (14) as a cocatalyst along with cobalt acetate [917-69-1] for the partial oxidation of alkyl side chains on polystyrene polymers (15) and as a sedative, hypnotic, and anticonvulsant. The FDA has, however, indicated that sodium bromide is ineffective as an over-the-counter sleeping aid for which it has been utilized (16). 

The common oxidants are ozone, hydrogen peroxide, H2O, catalyzed usually with ferrous iron, Fe , and ia some cases chlorine dioxide and uv light. Advanced oxidation systems iaclude H2O2 + uv ozone + uv and H2O2, ozone, and uv. Depending on the appHcation, the oxidation can be complete to end products as in a contaminated groundwater or partial to degradable intermediate products as in a process wastewater. 

We have summarized below recent results concerning spectroscopic / flow reactor investigations of hydrocarbons partial and total oxidation on different transition metal oxide catalysts. The aim of this study is to have more information on the mechanisms of the catalytic activity of transition metal oxides, to better establish selective and total oxidation ways at the catalyst surface, and to search for partial oxidation products from light alkane conversion. 

CAR [Combined autothermal reforming] A "reforming process for making "syngas from light hydrocarbons, in which the heat is provided by partial oxidation in a section of the reactor. Developed by Uhde and commercialized at an oil refinery at Strazske, Slovakia, in 1991. 

The partial oxidation method is normally used for heavier feedstocks, everything from naphtha to residual fuel, in those places where natural gas or light hydrocarbons (ethane, propane, or butane) are not readily available. 

Synthesis gas generation Process in which light hydrocarbons are partially oxidized over a catalyst at about 875 K with oxygen and the carbon monoxide is shifted with steam to produce CO and H. ... 

Numerous studies have been published on catalyst material directly related to rich catalytic combustion for GTapplications [73]. However, most data are available on the catalytic partial oxidation of methane and light paraffins, which has been widely investigated as a novel route to H2 production for chemical and, mainly, energy-related applications (e.g. fuel cells). Two main types of catalysts have been studied and are reviewed below supported nickel, cobalt and iron catalysts and supported noble metal catalysts. 

The direct reaction of methane partial oxidation always competes with total oxidation reactions, which are also responsible for O2 consumption, whereas steam and dry reforming and C-forming reactions are also to be considered. All reactions are catalyzed by the materials which are active in partial oxidation, but different scales of reactivity for the catalysts can be estimated from the experimental data. Total oxidation prevails at the light-off of the fuel-rich stream over most catalysts, but precious metals are more active than transition metals. 

In the past, coal or heavy hydrocarbon feedstock ammonia plants were not economically competitive with plants where the feedstocks were light hydrocarbons (natural gas to naphtha). Because of changing economics, however, plants that can handle heavy hydrocarbon feedstock are now attracting increasing attention- In addition, the continuous development and improvement of partial oxidation processes at higher pressure have allowed reductions in equipment size and cost. Therefore, the alternate feedback ammonia plants based on a partial oxidation process may become economically competitive in the near future. 

The continental biosphere is a large source of hydrocarbons. Quantification of these sources in toms of geophysical (e.g. temperature, humidity, light levels) and biogeochemical (soil physical and chemical properties, land use) parameters is much needed for inclusion in atmospheric models. The hydrocarbon oxidation mechanisms in the atmosphere should also be better understood, so that formation of ozone, carbon monoxide, partially oxidized gaseous hydrocarbons, and organic aerosol can be better quantified. The formation of organic aerosol from hydrocarbon precursors and then-capability to serve as cloud condensation nuclei are issues which need to be studied in depth. 

This has in turn been related to the relative stability of the OMME compared to the ethylene reactant and the epoxide product [11]. It has been argued that the relative instability of the OMME intermediate on Ag compared to Group VIII metals is the main origin of the unique activity of Ag as an effective epoxidation catalyst. Whether this simple interpretation is correct remains to be seen and will require considerable further investigations. In our current studies, we propose to shed light on the competitive partial oxidation and total oxidation channels with ab initio derived microkinetic modeling [61]. 

Process hydrogen is produced by steam reforming light hydrocarbon gases. An alternative method for hydrogen production is partial oxidation of the heavy vacuum bottoms stream or of coal. 

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