Of redox reactions

Step 3 A series of redox reactions converts chromium from the 4+ oxidation state m HCr03 to the 3 + oxidation state... 

The cure reaction of structural acrylic adhesives can be started by any of a great number of redox reactions. One commonly used redox couple is the reaction of benzoyl peroxide (BPO) with tertiary aromatic amines. Pure BPO is hazardous when dry [39]. It is susceptible to explosion from shock, friction or heat, and has an autoignition temperature of 79°C. Water is a very effective stabilizer for BPO, and so the initiator is often available as a paste or a moist solid [40], The... 

More detailed consideration of these various equilibria and other redox reactions of the halogen oxoacids will be found under the separate headings below. As expected, the rates of redox reactions of the halogen oxyanions will depend, sometimes crucially, on the precise conditions used. However, as a very broad generalization, they tend to become progressively faster as the oxidation state of the halogen decreases, i.e. ... 

In redox initiation, the free radicals that initiate the polymerization are generated as transient intermediates in the course of redox reaction. Essentially this involves an electron transfer process followed by scission to give free radicals. A wide variety of redox reactions, involving both organic and inorganic components either wholly... 

To a chemist, electrochemical cells are of interest primarily for the information they yield CENGAGENOW concerning the spontaneity of redox reactions, the strengths of oxidizing and reducing Click Chemistry Interactive for a self-study... 

The complex reacts with CO reversibly via a series of redox reactions. Rh(TMPP)2+ forms adducts with bulky isocyanides RNC (R = Bu , Pr ), retaining the +2 state but changing to a trans-geometry (Figure 2.34) with monodentate phosphines (and uncoordinated ethers) (R = Bu , Mefr = 2.04 B gj. = 2.45, g = 1.96). 

Further advances in the study of the mechanisms of redox reactions. A. G. Sykes, Adv. Inorg. Chem. Radiochem., 1967,10,153-245 (425). 

The donor-acceptor approach to solvent effects on the rates of redox reactions between different metal complexes, R. Schmid, Rev. Inorg. Chem., 1979,1,117-131 (48). 

Studies of ligands which might provide specificity in binding to various oxidation states of plutonium seems a particularly promising area for futher research. If specific ion electrodes could be developed for the other oxidation states, study of redox reactions would be much facilitated. Fast separation schemes which do not change the redox equilibria and function at neutral pH values would be helpful in studies of behavior of tracer levels of plutonium in environmental conditions. A particularly important question in this area is the role of PuOj which has been reported to be the dominant soluble form of plutonium in some studies of natural waters (3,14). 

There has therefore been much interest in the mediation of redox reactions in solution by conducting polymer-modified electrodes. 

What Do We Need to Know Already This chapter extends the thermodynamic discussion presented in Chapter 7. In particular, it builds on the concept of Gibbs free energy (Section 7.12), its relation to maximum nonexpansion work (Section 7.14), and the dependence of the reaction Gibbs free energy on the reaction quotient (Section 9.3). For a review of redox reactions, see Section K. To prepare for the quantitative treatment of electrolysis, review stoichiometry in Section L. 

We begin with a review of redox reactions, which were introduced in Section K. In this chapter we take a closer look at them and see how they can be used to generate electricity, particularly in aqueous solution. 

Mechanisms of Redox Reactions of Simple Chemistry H. Taube... 

Further Advances in the Study of Mechanisms of Redox Reactions A. G. Sykes... 

While these calculations provide information about the ultimate equilibrium conditions, redox reactions are often slow on human time scales, and sometimes even on geological time scales. Furthermore, the reactions in natural systems are complex and may be catalyzed or inhibited by the solids or trace constituents present. There is a dearth of information on the kinetics of redox reactions in such systems, but it is clear that many chemical species commonly found in environmental samples would not be present if equilibrium were attained. Furthermore, the conditions at equilibrium depend on the concentration of other species in the system, many of which are difficult or impossible to determine analytically. Morgan and Stone (1985) reviewed the kinetics of many environmentally important reactions and pointed out that determination of whether an equilibrium model is appropriate in a given situation depends on the relative time constants of the chemical reactions of interest and the physical processes governing the movement of material through the system. This point is discussed in some detail in Section 15.3.8. In the absence of detailed information with which to evaluate these time constants, chemical analysis for metals in each of their oxidation states, rather than equilibrium calculations, must be conducted to evaluate the current state of a system and the biological or geochemical importance of the metals it contains. 

Table 16-4 Examples of redox reactions, consisting of an oxidation and reduction half reaction...

The sulfur-rich oxides S 0 and S 02 belong to the group of so-called lower oxides of sulfur named after the low oxidation state of the sulfur atom(s) compared to the best known oxide SO2 in which the sulfur is in the oxidation state +4. Sulfur monoxide SO is also a member of this class but is not subject of this review. The blue-green material of composition S2O3 described in the older literature has long been shown to be a mixture of salts with the cations S4 and Ss and polysulfate anions rather than a sulfur oxide [1,2]. Reliable reviews on the complex chemistry of the lower sulfur oxides have been published before [1, 3-6]. The present review deals with those sulfur oxides which contain at least one sulfur-sulfur bond and not more than two oxygen atoms. These species are important intermediates in a number of redox reactions of elemental sulfur and other sulfur compounds. 

A detailed discussion of redox reactions must wait until Chapter 19, after we explore the nature of the atom, periodic properties of the elements, and thermodynamics. For now, we focus on only a few types of redox reactions that are common and relatively simple. 

We begin this chapter with a discussion of the principles of redox reactions, including redox stoichiometry. Then we introduce the principles of electrochemishy. Practical examples of redox chemistry, including corrosion, batteries, and metallurgy, appear throughout the chapter. 

The first step In balancing a redox reaction is to divide the unbalanced equation into half-reactions. Identify the participants in each half-reaction by noting that each half-reaction must be balanced. That Is, each element In each half-reaction must be conserved. Consequently, any element that appears as a reactant In a half-reaction must also appear among the products. Hydrogen and oxygen frequently appear in both half-reactions, but other elements usually appear In just one of the half-reactions. Water, hydronium ions, and hydroxide ions often play roles In the overall stoichiometry of redox reactions occurring in aqueous solution. Chemists frequently omit these species in preliminary descriptions of such redox reactions. 

Pourbaix diagrams for the aqueous Cd-S, Cd-Te, Cd-Se, Cu-In-Se, and Sb-S systems have been compiled and discussed by Savadogo [26] in his review regarding chemically and electrochemically deposited thin Aims for solar energy materials. Dremlyuzhenko et al. [27] analyzed theoretically the mechanisms of redox reactions in the Cdi xMn , Te and Cdi- , Zn i Te aqueous systems and evaluated the physicochemical properties of the semiconductor surfaces as a function of pH. 

The last two decades have seen a growing interest in the mechanism of inorganic reactions in solution. Nowhere is this activity more evident than in the topic covered by this review the oxidation-reduction processes of metal complexes. This subject has been reviewed a number of times previously, notably by Taube (1959), Halpern (1961), Sutin (1966), and Sykes (1967). Other articles and books concerned, wholly or partly, with the topic include those by Stranks, Fraser , Strehlow, Reynolds and Lumry , Basolo and Pearson, and Candlin et al ° Important recent articles on the theoretical aspects are those by Marcus and Ruff. Elementary accounts of redox reactions are included in the books by Edwards , Sykes and Benson . The object of the present review is to provide a more detailed survey of the experimental work than has hitherto been available. 

In the case of redox reactions, polarization also depends on the natme of the nonconsumable electrode at which a given reaction occms (for the equilibrium potential, to the contrary, no such dependence exists). Hence, the term reaction will be understood as reaction occurring at a specified efectrode. ... 

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