Oxidation of chemical compounds

Chemoautotroph An organism that obtains its energy from the oxidation of chemical compounds and uses only organic compounds as a source of carbon. Example nitrifiers. 

Chemotroph An organism that obtains its energy from the oxidation of chemical compounds. 

Therefore, consideration will here be restricted to a few comments regarding the shape of the layer thickness-time dependence. First, the most probable dependence in the case of formation of non-volatile chemical compounds between solid A and gas B will be analysed, assuming that at a given temperature B is insoluble in A. Then, the influence of evaporation on the layer-growth kinetics will be illustrated. Also, soft oxidation of chemical compounds will briefly be considered. 

Most organisms, however, are unable to use radiant forms of energy and rely instead on the oxidation of chemical compounds as a source of energy. These organisms (called chemotrophs) are divided in two groups on the basis of the type of... 

Lactic acid bacteria are chemotrophic they find the energy required for their entire metabolism from the oxidation of chemical compounds. The oxidation of substrates represents the loss of electrons that must be accepted by another molecule, which is reduced. Most oxidations, simultaneously liberate... 

Chemical ingenuity in using the properties of the elements and their compounds has allowed analyses to be carried out by processes analogous to the generation of hydrides. Osmium tetroxide is very volatile and can be formed easily by oxidation of osmium compounds. Some metals form volatile acetylacetonates (acac), such as iron, zinc, cobalt, chromium, and manganese (Figure 15.4). Iodides can be oxidized easily to iodine (another volatile element in itself), and carbonates or bicarbonates can be examined as COj after reaction with acid. 

Olefins are the basic building blocks for many chemical syntheses. These unsaturated materials enter into polymers, rubbers, and plastics, and react to form a wide variety of chemical compounds such as alcohols, amines, chlorides and oxides. 

This limited survey has indicated the wide range of chemical compounds, particularly oxides, which may be formed on a metal surface as a result of a corrosion process. The nature of such films and scales needs to be carefully characterised. Fortunately, a wide spectrum of experimental techniques is now available to provide such valuable information, and others are under development. A convenient summary is provided in Table 1.6. 

Lead forms two types of chemical compounds lead (II), and lead (IV) compounds based on Pb24 and Pb4 ions, where those based on Pb2 ions are the more stable. The metal is oxidized even at room temperature to lead oxide (PbO) and also by water that contains oxygen and forms lead hydroxide (Pb(OH),). In the lead-acid battery, the (less stable) lead (IV) oxide (lead dioxide, Pb02), is of greatest importance. Beside these two, a number of oxides are observed in the battery that are mostly mixtures. A brief survey will now be given of those compounds that are of interest for lead-acid batteries. 

Conversely, the use of elevated temperatures will be most advantageous when the current is determined by the rate of a preceding chemical reaction or when the electron transfer occurs via an indirect route involving a rate-determining chemical process. An example of the latter is the oxidation of amines at a nickel anode where the limiting current shows marked temperature dependence (Fleischmann et al., 1972a). The complete anodic oxidation of organic compounds to carbon dioxide is favoured by an increase in temperature and much fuel cell research has been carried out at temperatures up to 700°C. 

In the introductory chapter we stated that the formation of chemical compounds with the metal ion in a variety of formal oxidation states is a characteristic of transition metals. We also saw in Chapter 8 how we may quantify the thermodynamic stability of a coordination compound in terms of the stability constant K. It is convenient to be able to assess the relative ease by which a metal is transformed from one oxidation state to another, and you will recall that the standard electrode potential, E , is a convenient measure of this. Remember that the standard free energy change for a reaction, AG , is related both to the equilibrium constant (Eq. 9.1)... 

For reviews, see Hudlicky, M. Oxidations in Organic Chemistry, American Chemical Society Washington, 1990, p. 67 Haines, A.H. Methods for the Oxidation of Organic Compounds Academic Press NY, 1985, pp. 73, 278 Sheldon, R.A. Kochi, J.K. Metal-Catalyzed Oxidations of Organic Compounds Academic Press NY, 1981, pp. 162, 294. For a list of reagents, with references, see Ref. 150, p. 494. 

In a similar way, electrochemistry may provide an atomic level control over the deposit, using electric potential (rather than temperature) to restrict deposition of elements. A surface electrochemical reaction limited in this manner is merely underpotential deposition (UPD see Sect. 4.3 for a detailed discussion). In ECALE, thin films of chemical compounds are formed, an atomic layer at a time, by using UPD, in a cycle thus, the formation of a binary compound involves the oxidative UPD of one element and the reductive UPD of another. The potential for the former should be negative of that used for the latter in order for the deposit to remain stable while the other component elements are being deposited. Practically, this sequential deposition is implemented by using a dual bath system or a flow cell, so as to alternately expose an electrode surface to different electrolytes. When conditions are well defined, the electrolytic layers are prone to grow two dimensionally rather than three dimensionally. ECALE requires the definition of precise experimental conditions, such as potentials, reactants, concentration, pH, charge-time, which are strictly dependent on the particular compound one wants to form, and the substrate as well. The problems with this technique are that the electrode is required to be rinsed after each UPD deposition, which may result in loss of potential control, deposit reproducibility problems, and waste of time and solution. Automated deposition systems have been developed as an attempt to overcome these problems. 

Thus, we considered a number of examples of application of the sensor technique in experiments on heterogeneous recombination of active particles, pyrolysis and photolysis of chemical compounds in gas phase and on the surface of solids, such as oxides of metals and glasses. The above examples prove that, in a number of cases, compact detectors of free atoms and radicals allow one to reveal essential elements of the mechanisms of the processes under consideration. Moreover, this technique provides new experimental data, which cannot be obtained by other methods. Sensors can be used for investigations in both gas phase and adsorbed layers. This technique can also be used for studying several types of active particles. It allows one to determine specific features of distribution of the active particles along the reaction vessel. The above experiments demonstrate inhomogeneity of the reaction mixture for the specified processes and, consequently, inhomogeneity of the... 

Palmisano, G., Addamo, M., Augugliaro, V., Caronna, T., Garci a-Lopez, E., Loddo, V., and Palmisano, L. (2006) Influence of the substituent on selective photocatalytic oxidation of aromatic compounds in aqueous Ti02 suspensions. Chemical Communications (9), 1012-1014. 

The improvement of its activity and stability has been approach by the use of GE tools (see Refs. [398] and [399], respectively). A process drawback is the fact that the oxidation of hydrophobic compounds in an organic solvent becomes limited by substrate partition between the active site of the enzyme and the bulk solvent [398], To provide the biocatalyst soluble with a hydrophobic active site access, keeping its solubility in organic solvents, a double chemical modification on horse heart cytochrome c has been performed [400,401], First, to increase the active-site hydrophobicity, a methyl esterification on the heme propionates was performed. Then, polyethylene glycol (PEG) was used for a surface modification of the protein, yielding a protein-polymer conjugates that are soluble in organic solvents. 

A substance which results in the chemical inactivation of a metal. The catalytic effect of heavy metals, mainly copper and manganese, on the oxidation of unsaturated compounds such as rubber, results in very rapid deterioration. Chelating agents convert the metal into a chelate co-ordination compound and thus render the metal inactive. The term sequestering agents has been applied to chelating agents but this infers that the metal has been removed and not merely inactivated. 

The phenomenon of chemical induction was intensively studied by Jorissen [33-37]. He discovered that indigo was not oxidized by dioxygen but was simultaneously oxidized in the presence of oxidized triethylphosphine or benzaldehyde. He measured the factor of chemical induction in these reactions as equal to unity. Later, he proved that the oxidation product of benzaldehyde, benzoic peracid, did not oxidize indigo under conditions of experiment. This shows that a very active intermediate was formed during the oxidation of benzaldehyde and that it was not perbenzoic acid. Engler assumed peroxide to be in two forms, namely, an active moloxide A02 and a more stable peroxide. A new correct interpretation of chemical induction in oxidation reactions was provided later by the chain theory of oxidation of organic compounds (see later). 

If hydroperoxide is the main autoinitiator, oxidation can be retarded by the introduction of chemical compounds capable to decompose hydroperoxide without the formation of free radicals. 

EM Pliss. Oxidation of vinyl compounds mechanism, elementary reactions, structure and reactivity, Doctoral Thesis, Institute of Chemical Physics, Chernogolovka, 1990, pp. 1-40 [in Russian]. 

The catalytic additives that have been investigated in MgH can be roughly divided into three important groups metals/intermetallics, oxides, and chemical compounds that include hydrides. Their effect on the desorption properties of MgH will be discussed in the following sections. We are not going to discuss absorption since, as mentioned before, absorption is usually much easier than desorption. 

A broad spectrum of chemical reactions can be catalyzed by enzymes Hydrolysis, esterification, isomerization, addition and elimination, alkylation and dealkylation, halogenation and dehalogenation, and oxidation and reduction. The last reactions are catalyzed by redox enzymes, which are classified as oxidoreductases and divided into four categories according to the oxidant they utilize and the reactions they catalyze 1) dehydrogenases (reductases), 2) oxidases, 3) oxygenases (mono- and dioxygenases), and 4) peroxidases. The latter enzymes have received extensive attention in the last years as bio catalysts for synthetic applications. Peroxidases catalyze the oxidation of aromatic compounds, oxidation of heteroatom compounds, epoxidation, and the enantio-selective reduction of racemic hydroperoxides. In this article, a short overview... 

The energy in food is in the form of carbohydrate, fat and protein, and the oxidation of these compounds, in vitro, transfers the chemical energy into heat which can then be measured. This is done in what is known as a bomb calorimeter (Figure 2.1). The heat released in the calorimeter when 1 g of carbohydrate, fat, protein or other fuel is fully oxidised (i.e. Af/) is given in Table 2.3. 

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