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Catalysts, chemical activity

Peroxyoxalate. The chemical activation of a fluorescer by the reactions of hydrogen peroxide, a catalyst, and an oxalate ester has been the object of several mechanism studies. It was first proposed in 1967 that peroxyoxalate (26) was converted to dioxetanedione (27), a highly unstable intermediate which served as the chemical activator of the fluorescer (fir) (6,9). [Pg.266]

The binder system of a plastic encapsulant consists of an epoxy resin, a hardener or curing agent, and an accelerating catalyst system. The conversion of epoxies from the Hquid (thermoplastic) state to tough, hard, thermoset soHds is accompHshed by the addition of chemically active compounds known as curing agents. Flame retardants (qv), usually in the form of halogens, are added to the epoxy resin backbone because epoxy resins are inherently flammable. [Pg.530]

Catalysts that do not contain potassium lose activity very quickly because of coke deposition on the surface of the catalyst. Chemical changes that occur when the catalyst is removed from the operating environment make it very difficult to determine the nature of most of the promoter elements during the reaction, but potassium is always found to be present as potassium carbonate in the used catalyst. The other promoters are claimed to increase selectivity and the operating stabiUty of the catalyst. [Pg.198]

Reactions that are catalyzed by solids occur on the surfaces of the solids at points of high chemical activity. Therefore, the activity of a catalytic surface is proportional to the number of active centers per unit area. In many cases, the concentration of active centers is relatively low. This is evident by the small quantities of poisons present (material that retards the rate of a catalytic reaction) that are sufficient to destroy the activity of a catalyst. Active centers depend on the interatomic spacing of the solid structure, chemical constitution, and lattice structure. [Pg.11]

Sulfided Mo and Co-Mo catalysts, used in hydrotreating reactions, contain Mo as M0S2. This compound has a layer structure consisting of sandwiches, each of a Mo layer between two S layers. The chemical activity of M0S2 is associated with the edges of the sandwich where the Mo is exposed to the gas phase the basal plane of the anions is... [Pg.157]

A system has been constructed which allows combined studies of reaction kinetics and catalyst surface properties. Key elements of the system are a computer-controlled pilot plant with a plug flow reactor coupled In series to a minireactor which Is connected, via a high vacuum sample transfer system, to a surface analysis Instrument equipped with XFS, AES, SAM, and SIMS. When Interesting kinetic data are observed, the reaction Is stopped and the test sample Is transferred from the mlnlreactor to the surface analysis chamber. Unique features and problem areas of this new approach will be discussed. The power of the system will be Illustrated with a study of surface chemical changes of a Cu0/Zn0/Al203 catalyst during activation and methanol synthesis. Metallic Cu was Identified by XFS as the only Cu surface site during methanol synthesis. [Pg.15]

The development of modern surface characterization techniques has provided means to study the relationship between the chemical activity and the physical or structural properties of a catalyst surface. Experimental work to understand this reactivity/structure relationship has been of two types fundamental studies on model catalyst systems (1,2) and postmortem analyses of catalysts which have been removed from reactors (3,4). Experimental apparatus for these studies have Involved small volume reactors mounted within (1) or appended to (5) vacuum chambers containing analysis Instrumentation. Alternately, catalyst samples have been removed from remote reactors via transferable sample mounts (6) or an Inert gas glove box (3,4). [Pg.15]

By single-site catalysts we mean catalysts where the breaking and formation of chemical bonds occurs at isolated active centers whose chemical activity is dominated by the electronic properties of a single atomic species or of a small cluster of atoms that can act in an independent way with respect to others. [Pg.38]

Many different topics are involved in the study of metallic nanoparticles and many fundamental issues can be present for example, which is the infiuence of the nanoparticle size, shape and composition on the chemical activity of heterogeneous catalysts Or, considering another problem, at what size does a small particle behave like the bulk material, for example, changing from an insulator to a semiconductor [9-12] An enormous amount of literature is published on metallic nanoclusters this review is focusing on the relevant problem concerning the characterization of metallic nanosized materials from the morphological and... [Pg.129]

This last equation contains the two essential activation terms met in electrocatalysis an exponential function of the electrode potential E and an exponential function of the chemical activation energy AGj (defined as the activation energy at the standard equilibrium potential). By modifying the nature and structure of the electrode material (the catalyst), one may decrease AGq, thus increasing jo, as a result of the catalytic properties of the electrode. This leads to an increase in the reaction rate j. [Pg.346]

Like the carbodiimide method, the mixed anhydride method results in an amide complex (Table 5, Figure 17). The acid-containing hapten is dissolved in a dry, inert, dipolar, aprotic solvent such as p-dioxane, and isobutyl chloroformate is added with an amine catalyst. The activated mixed anhydride is chemically stable and can be isolated and characterized. The aqueous protein solution is added to the activated acid and the pH is maintained at around 8.5. A low temperature (around 10 °C) is necessary during the reaction to minimize side reactions. [Pg.641]

The chemicals used, resorcinol, aniline, NaN02, HCl, NaOH and solvents were all technical grade materials. The palladium catalysts were activated carbon supported ones, all commercial products (see Table 14.1). [Pg.128]

Generally radical acceptors or oxidation catalysts, which effectively remove free radicals formed during milling and mixing procedures. Inter-macromolecular action leads to reduction of the entanglements between polymer molecules. Chemically activated zinc soaps. [Pg.782]

Catalysts were activated before reaction at 450°C in N2 flow for 3 hours. Software Spartan Pro has been used for the quantum chemical semi-empirical (type AM 1) calculation of transition states energies. [Pg.356]

Not only kinetics but also the role of polar catalysts like water increasingly was viewed as the cause of chemical activation, as we will see later. In his paper at the 1925 Solvay conference, Job brought into strong focus the role... [Pg.145]

Aside from thermal interactions, chemical interactions between flames and surfaces are also important. Chemical interactions are typically manifested either by radical recombination on cold (relatively inert) walls [4, 5] or by heterogeneous combustion on chemically active surfaces (catalysts). Among the available technologies, catalysts have the best potential for NO, reduction. A review on recent advances in catalytic combustion is given elsewhere [6]. The focus here is on combustion near inert surfaces. [Pg.427]


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See also in sourсe #XX -- [ Pg.103 ]




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