Carbon/transition metal oxide

The results from Fig. 12 suggest a general reaction mechanism in mixtures involving CO32-ions in fact, in addition to the systems presented in this chapter, the carbonate complex was identified in a number of other alkaline-carbonate-transition-metal oxide mixtures, including the following ... 

Alkali metal haHdes can be volatile at incineration temperatures. Rapid quenching of volatile salts results in the formation of a submicrometer aerosol which must be removed or else exhaust stack opacity is likely to exceed allowed limits. Sulfates have low volatiHty and should end up in the ash. Alkaline earths also form basic oxides. Calcium is the most common and sulfates are formed ahead of haHdes. Calcium carbonate is not stable at incineration temperatures (see Calcium compounds). Transition metals are more likely to form an oxide ash. Iron (qv), for example, forms ferric oxide in preference to haHdes, sulfates, or carbonates. SiHca and alumina form complexes with the basic oxides, eg, alkaH metals, alkaline earths, and some transition-metal oxidation states, in the ash. 

The formation of polyesters from carbon monoxide and propylene oxide using a cobalt catalyst may involve an alternate coordination on the metal and an insertion of monomers into the carbon-transition metal bond240. ... 

Destruction of chlorinated organic solvents in a molten carbonate with transition metal oxides... 

Oxidative Cleavage of Carbon-Carbon Double Bonds 12.4.1. Transition Metal Oxidants... 

In supercapacitors, apart from the electrostatic attraction of ions in the electrode/electrolyte interface, which is strongly affected by the electrochemically available surface area, pseudocapacitance effects connected with faradaic reactions take place. Pseudocapacitance may be realized through carbon modification by conducting polymers [4-7], transition metal oxides [8-10] and special doping via the presence of heteroatoms, e.g. oxygen and/or nitrogen [11, 12]. 

Other successful but limited surface modifying trials have been done such as Pt dispersed onto Ti02, Pt-Co and Mn perovskite , Pt-transition metal oxides , Pt-Au-Fe203 or Ru02- These materials are known as gas-solid interface carbon monoxide catalysts and have been... 

In 1971, LDHs containing different metal cations (such as Mg, Zn, Ni, Cr, Co, Mn and Al) with carbonate as interlayer anions, calcined at 473-723 K and partially or completely chlorinated, were reported to be effective as supports for Ziegler catalysts in the polymerization of olefins [8], with the maximum catalytic activity of polyethylene production observed for Mg/Mn/Al - CO3 LDH calcined at 473 K. Even earher, calcined Mg/Al LDHs were used to support Ce02 for SO removal from the emissions from fluidized catalytic cracking units (FCCU) [9,10]. Some transition metal oxides have also been... 

Application of transmission electron microscopy (TEM) techniques on heterogeneous catalysis covers a wide range of solid catalysts, including supported metal particles, transition metal oxides, zeolites and carbon nanotubes and nanofibers etc. 

Figure 1. Schematic description of a (lithium ion) rocking-chair cell that employs graphitic carbon as anode and transition metal oxide as cathode. The undergoing electrochemical process is lithium ion deintercalation from the graphene structure of the anode and simultaneous intercalation into the layered structure of the metal oxide cathode. For the cell, this process is discharge, since the reaction is spontaneous.

In the following section, we restrict our discussion to templated mesoporous solids that are of potential interest as battery electrodes, including many transition-metal oxides and carbon. This slice of the literature still points the interested reader to many articles on the synthesis and physical characterization of relevant mesoporous materials. A much smaller number of electrochemical studies with templated mesoporous electrodes have been published, and these studies in particular will be noted. 

The oxidation of carbon on the catalyst surface proceeds through formation of solid surface oxides that decompose to CO and CO2 as primary products. Previous studies have shown the CO2/CO ratio at the catalyst surface is a function of temperature (Arthur s Ratio) and is typically 1.0 for FCC catalyst and conditions [3]. However, the CO exiting the bum site can be further oxidized to CO2 at a rate dependent on temperature, CO, O2, H2O, active metals on the catalyst, and even the presence of the catalyst itself. Also, transition metal oxides have been found to increase the coke... 

Although a majority of these composite thermistors are based upon carbon black as the conductive filler, it is difficult to control in terms of particle size, distribution, and morphology. One alternative is to use transition metal oxides such as TiO, VO2, and V2O3 as the filler. An advantage of using a ceramic material is that it is possible to easily control critical parameters such as particle size and shape. Typical polymer matrix materials include poly(methyl methacrylate) PMMA, epoxy, silicone elastomer, polyurethane, polycarbonate, and polystyrene. 

Carbon monoxide in the product is not inert and may change the stoichiometry and properties of transition metal oxide pigment or magnetic ferrites, such as Fe203. 

Olefinic compounds will often insert into carbon-transition metal bonds as CO does, and this reaction is an important step in many catalytic syntheses. When this step is combined with an oxidative addition of an organic halide to a palladium(O) complex in the presence of a base, a very useful, catalytic olefinic substitution reaction results (26-29). The oxidative addition produces an organopalladium(II) halide, which then adds 1,2 to the olefinic reactant (insertion reaction). The adduct is unstable if there are hydrogens beta to the palladium group and elimination of a hydridopalladium salt occurs, forming a substituted olefinic product. The hydridopalladium salt then reforms the... 

In order to elucidate the importance of the role of in situ formed carbon in the formation of well-organized, highly crystalline mesoporous transition metal oxides, as-synthesized Ti02 was directly calcined under air to 700°C while keeping all other conditions the same as for the CASH method. As expected, the BET surface area of the resulting material was only 0.2 m2 g-1 and no porous structure could be detected by TEM imaging. This implies that the mesostructure completely collapsed. The crystallite size of this sample, heat treated to 700°C in air is 31.5 nm (calculated... 

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