Decomposition on metals

D. Reactions for Formic Acid Decomposition ON Metal-Adlayer Surfaces... 

Baba R, Nakabayashi S, Fujishima A, Honda K (1985) Investigation of the mechanism of hydrogen evolution during photocatalytic water decomposition on metal-loaded semiconductor powders J Phys Chem 89 1902-1905... 

For the formate radical HCOO, we use Eq. (10b) with DAB =110 kcal/ mol for the 171 coordination and Eq. (20b) with DAX = 166 kcal/mol for the rj1 coordination. We have calculated the relevant values of (2hcoo f°r Ag(lll), Ni(lll), Fe(110), and W(110). Because no direct experimental data are available, we shall discuss our projections later in the general context of HCOOH decomposition on metal surfaces. Here we shall only mention that for HCOO the 172 coordination was found to be always preferred over the 17 coordination, in full agreement with experiment (see Section IV,C). 

The formic acid decomposition on metal catalysts accordingly seems to proceed via surface formate, though the difference in basicity of the metal surface would result in different coverage during the reaction, which in turn leads to a different reaction order. It is widely known that Fahrenfort et al. 34) thus correlated the catal3d ic activities of the... 

At P02 = 0.3 atm, 2 n20 = 0-1 atm, and 750°C, e.g., Uo(st) = 1.2 ao(eq) has been observed. Thus, Uo(st) is close to the equilibrium value for reaction (V.24). Although the deviation between o(st) and ao(eq) is small, this deviation yields a definite clue regarding the prevailing mechanism. The rate of N2O decomposition on metal oxides is in essence proportional to the partial pressure of N2O. Thus, one may assume that the decomposition of an adsorbed N2O molecule into N2 and an adsorbed oxygen atom is the primary step,... 

A couple of very recent examples are available in the literature of the use of laser-based extraction methodologies for the analysis of EEIs. The motivation for the use of lasers was different in both cases. In one case, matrix-assisted laser desorp-tion/ionization (MALDI) coupled with MS was employed to collect evidence of solvent oligomerization during decomposition on metallic surfaces [24], This technique is popular within the organic chemistry community for its sensitivity and... 

Shustorovich E, Bell AT (1989) An analysis of formic acid decomposition on metal surfaces by the bond-order-conservation-order-potential approach. Surface Sci 222 371-382... 

Sheppard N and De La Cruz C 1998 Vibrational spectra of hydrocarbons adsorbed on metals. Part II. Adsorbed acyclic alkynes and alkanes, cyclic hydrocarbons including aromatics and surface hydrocarbon groups derived from the decomposition of alkyl halides, etc Adv. Catal. 42 181-313... 

High Purity Aluminum Trifluoride. High purity anhydrous aluminum triduoride that is free from oxide impurities can be prepared by reaction of gaseous anhydrous HF and AlCl at 100°C, gradually raising the temperature to 400°C. It can also be prepared by the action of elemental fluorine on metal/metal oxide and subsequent sublimation (12) or the decomposition of ammonium duoroaluminate at 700°C. 

The radicals are then involved in oxidations such as formation of ketones (qv) from alcohols. Similar reactions are finding value in treatment of waste streams to reduce total oxidizable carbon and thus its chemical oxygen demand. These reactions normally are conducted in aqueous acid medium at pH 1—4 to minimize the catalytic decomposition of the hydrogen peroxide. More information on metal and metal oxide-catalyzed oxidation reactions (Milas oxidations) is available (4-7) (see also Photochemical technology, photocatalysis). 

Condensation of metal vapors followed by deposition on cooler surfaces yields metal powders as does decomposition of metal hydrides. Vacuum treatment of metal hydrides gives powders of fine particle size. Reaction of a metal haHde and molten magnesium, known as the KroU process, is used for titanium and zirconium. This results in a sponge-like product. 

High purity stibiae is used as an -type, gas-phase dopant for Si in semiconductors (14). Low temperature distillation of stibiae at <53.3 kPa (400 torr) yields a product that on decomposition gives metallic antimony having less than 8 x lO " % impurity (18). A method for determining quantities of stibiae in the neighborhood of 0.1 mg/m in air has been reported (19). 

Corrosion products and deposits. All sulfate reducers produce metal sulfides as corrosion products. Sulfide usually lines pits or is entrapped in material just above the pit surface. When freshly corroded surfaces are exposed to hydrochloric acid, the rotten-egg odor of hydrogen sulfide is easily detected. Rapid, spontaneous decomposition of metal sulfides occurs after sample removal, as water vapor in the air adsorbs onto metal surfaces and reacts with the metal sulfide. The metal sulfides are slowly converted to hydrogen sulfide gas, eventually removing all traces of sulfide (Fig. 6.11). Therefore, only freshly corroded surfaces contain appreciable sulfide. More sensitive spot tests using sodium azide are often successful at detecting metal sulfides at very low concentrations on surfaces. 

Fig. 5. Acetylene decomposition on Co-HY (973 K, 30 minutes) (a) encapsulated metal particle (b) carbon filaments (A) and tubules of small diameters (B) on the surface of the catalyst.

Nitrogen forms binary compounds with almost all elements of the periodic table and for many elements several stoichiometries are observed, e.g. MnN, Mn Ns, Mn3N2, MniN, Mn4N and Mn tN (9.2 < jc < 25.3). Nitrides are frequently classified into 4 groups salt-like , covalent, diamond-like and metallic (or interstitial ). The remarks on p. 64 concerning the limitations of such classifications are relevant here. The two main methods of preparation are by direct reaction of the metal with Ni or NH3 (often at high temperatures) and the thermal decomposition of metal amides, e.g. ... 

Arsine, AsHs, is formed when many As-containing compounds are reduced with nascent hydrogen and its decomposition on a heated glass surface to form a metallic mirror formed the basis of Marsh s test for the element. The low-temperature reduction of AsCls with LiAlH4 in diethyl ether solution gives good yields of the gas as does the dilute acid hydrolysis of many arsenides of electropositive elements (Na, Mg, Zn, etc.). Similar reactions yield stibine, e.g. ... 

It is convenient to classify here the decompositions of metal salts of the various oxyhalogen acids on the basis of the oxygen content of the anion, with subsections devoted to the metals of a particular sub-group of the Periodic Table. Again, consideration of the ammonium salts is deferred to Sect. 4. As noted elsewhere in this review, some reports are not explicit as to whether or not melting accompanies reaction thermal analysis studies can be valuable [843]. 

Kinetic studies of the decomposition of metal formates have occasionally been undertaken in conjunction with investigations of the mechanisms of the heterogeneous decomposition of formic acid on the metal concerned. These comparative measurements have been expected to give information concerning the role of surface formate [522] (dissociatively adsorbed formic acid) in reactions of both types. Great care is required,... 

There is an extensive literature relating to the role of surface intermediates in the heterogeneous catalytic decomposition of formic acid on metals and oxides (see Refs. 36, 522,1030,1042—1045). 

It is believed [1135,1136] that the decomposition of metal complexes of salicyaldoxime and related ligands is not initiated by scission of the coordination bond M—L, but by cleavage of another bond (L—L) in the chelate ring which has been weakened on M—L bond formation. Decomposition temperatures and values of E, measured by several non-isothermal methods were obtained for the compounds M(L—L)2 where M = Cu(II), Ni(II) or Co(II) and (L—L) = salicylaldoxime. There was parallel behaviour between the thermal stability of the solid and of the complex in solution, i.e. Co < Ni < Cu. A similar parallel did not occur when (L—L) = 2-indolecarboxylic acid, and reasons for the difference are discussed... 

Wagner was first to propose the use of solid electrolytes to measure in situ the thermodynamic activity of oxygen on metal catalysts.17 This led to the technique of solid electrolyte potentiometry.18 Huggins, Mason and Giir were the first to use solid electrolyte cells to carry out electrocatalytic reactions such as NO decomposition.19,20 The use of solid electrolyte cells for chemical cogeneration , that is, for the simultaneous production of electrical power and industrial chemicals, was first demonstrated in 1980.21 The first non-Faradaic enhancement in heterogeneous catalysis was reported in 1981 for the case of ethylene epoxidation on Ag electrodes,2 3 but it was only... 

At high alkali coverages (near monolayer coverage), when the adsorbed alkali overlayer shows a metal-like character, alkali-methoxy species are formed. As shown by TPD experiments in the system K/Ru(001) these alkali-methoxy species are more stable than the methoxy species on clean Ru(001) and adsorbed methanol on 0.1K/Ru(001). On metal surfaces inactive for methanol decomposition, e.g. Cu(lll), these alkali-methoxy species are formed even at low alkali coverages, due to the weaker interaction of the alkali atoms with the metal surface. The formation of these species stabilizes the methoxy species on the metal surface and enhances the activity of the metal surface for methanol decomposition. 

The effect of electronegative additives on the adsorption of ethylene on transition metal surfaces is similar to the effect of S or C adatoms on the adsorption of other unsaturated hydrocarbons.6 For example the addition of C or S atoms on Mo(100) inhibits the complete decomposition (dehydrogenation) of butadiene and butene, which are almost completely decomposed on the clean surface.108 Steric hindrance plays the main role in certain cases, i.e the addition of the electronegative adatoms results in blocking of the sites available for hydrocarbon adsorption. The same effect has been observed for saturated hydrocarbons.108,109 Overall, however, and at least for low coverages where geometric hindrance plays a limited role, electronegative promoters stabilize the adsorption of ethylene and other unsaturated and saturated hydrocarbons on metal surfaces. 

The influence of the presence of sulfur adatoms on the adsorption and decomposition of methanol and other alcohols on metal surfaces is in general twofold. It involves reduction of the adsorption rate and the adsorptive capacity of the surface as well as significant modification of the decomposition reaction path. For example, on Ni(100) methanol is adsorbed dissociatively at temperatures as low as -100K and decomposes to CO and hydrogen at temperatures higher than 300 K. As shown in Fig. 2.38 preadsorption of sulfur on Ni(100) inhibits the complete decomposition of adsorbed methanol and favors the production of HCHO in a narrow range of sulfur coverage (between 0.2 and 0.5). 

On photolyzing CoziCOg in the matrix (20), a number of photoproducts could be observed. The results of these experiments are summarized in Scheme 4, which illustrates the various species formed. Of particular interest is the formation of Co2(CO)7 on irradiation of Co2(CO)g in CO (254 nm), as this species had not been characterized in the metal-atom study of Hanlan et al. (129). Passage of Co2(CO)g over an active, cobalt-metal surface before matrix isolation causes complete decomposition. On using a less active catalyst, the IR spectrum of Co(CO)4 could be observed. An absorption due to a second decomposition product, possibly Co2(CO)g, was also noted. 

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