Liquid-solid heterogeneous catalysis

The series of 10 chapters that constitute Part 3 of the book deals mainly with the use of adsorption as a means of characterizing carbons. Thus, the first three chapters in this section complement each other in the use of gas-solid or liquid-solid adsorption to characterize the porous texture and/or the surface chemistry of carbons. Porous texture characterization based on gas adsorption is addressed in Chapter 11 in a very comprehensive manner and includes a description of a number of classical and advanced tools (e.g., density functional theory and Monte Carlo simulations) for the characterization of porosity in carbons. Chapter 12 illustrates the use of adsorption at the liquid-solid interface as a means to characterize both pore texture and surface chemistry. The authon propose these methods (calorimetry, adsorption from solution) to characterize carbons for use in such processes as liquid purification or liquid-solid heterogeneous catalysis, for example. Next, the surface chemical characterization of carbons is comprehensively treated in Chapter 13, which discusses topics such as hydrophilicity and functional groups in carbon as well as the amphoteric characteristics and electrokinetic phenomena on carbon surfaces. 

In catalysis, oxides with well defined acidic and basic properties are used in different forms that have found application in numerous catalytic applications in the gas-solid and liquid-solid heterogeneous catalysis [3, 46, 47], Among the most used oxide materials in catalysis, we And (i) bulk oxides (one component metal oxides) (ii) doped and moditied oxides (iii) supported metal oxides (dispersed active oxide component onto a support oxide component) (iv) bulk and supported binary metal oxides to quaternary metal oxides (mixed oxide compositions) (v) complex oxides (e.g., spinels, perovskites, hexa-aluminates, bulk and supported hydrotalcites, pillared clays, bulk and supported heteropolyacids, layered silicas, etc.). 

Heterogeneous catalysts have different ability in the chemical transformation of reagents to form the desired reaction products due to various functionalities present at their surface. When reactions run in liquid by a liquid-solid heterogeneous catalysis, not only the characteristics of the surface (hydrophobic or hydrophilic surface) but the liquid properties (polarity, proticity, solvating ability) govern the process reactivity. 

Roberts, G. W. The influence of mass and heat transfer on the performance of heterogeneous catalysts in gas/liquid/solid systems. Catalysis in Organic Synthesis, Academic Press, (1976), pp. 1-44. 

Abstract Attention should be devoted to the measurements of the adsorption properties of catalytic surfaces when they have to work in liquid-solid heterogeneous conditions. The mutual characteristics of the surface and the liquid affect the reagent interactions with the surface sites which could be engaged with the liquid interaction and then not-available for the reagent coordination. This leads to observe effective adsorption properties that could be different from the intrinsic properties of the surface. The possibility to quantitatively determine the effective acid properties of catalytic surfaces by base adsorption is here showed. The adsorption can proceed in any type of liquid of various characteristics (apolar, polar, aprotic, protic) with dynamic (pulse liquid chromatographic method) or equilibrium (liquid recirculation chromatographic method) methods. The measurements of effective acidity allows finding more sound relations with the catalytic activity for a better comprehension of the catalyst work and for a more correct determination of the turnover numbers in liquid-solid catalysis. 

There has been a general updating of the material in all the chapters the treatment of films at the liquid-air and liquid-solid interfaces has been expanded, particularly in the area of contemporary techniques and that of macromolecular films. The scanning microscopies (tunneling and atomic force) now contribute more prominently. The topic of heterogeneous catalysis has been expanded to include the well-studied case of oxidation of carbon monoxide on metals, and there is now more emphasis on the flexible surface, that is, the restructuring of surfaces when adsorption occurs. New calculational methods are discussed. 

Catalysis in a single fluid phase (liquid, gas or supercritical fluid) is called homogeneous catalysis because the phase in which it occurs is relatively unifonn or homogeneous. The catalyst may be molecular or ionic. Catalysis at an interface (usually a solid surface) is called heterogeneous catalysis, an implication of this tenn is that more than one phase is present in the reactor, and the reactants are usually concentrated in a fluid phase in contact with the catalyst, e.g., a gas in contact with a solid. Most catalysts used in the largest teclmological processes are solids. The tenn catalytic site (or active site) describes the groups on the surface to which reactants bond for catalysis to occur the identities of the catalytic sites are often unknown because most solid surfaces are nonunifonn in stmcture and composition and difficult to characterize well, and the active sites often constitute a small minority of the surface sites. 

A very important part of such an undertaking is to be clear about what stages of a chemical process generate the most waste. Often this is found to be the separation stage, after the transformation of reactants to products, where all the various components of the final mixture are separated and purified. Approaches to chemical reactions which help to simplify this step are particularly powerful. Such an approach is exemplified by heterogeneous catalysis. This is an area of chemistry where the catalysts used are typically solids, and the reactants are all in the hquid or gas phase. The catalyst can speed up the reaction, increase the selectivity of the reaction, and then be easily recovered by filtration from the liquid, and reused. 

In homogeneous catalysis soluble catalysts are applied, usually in the liquid phase, in contrast to heterogeneous catalysis, where solid catalysts are used. Homogeneous catalysis is applied in many processes in both bulk and fine chemicals production. 

In order to overcome these problems, attention was focused on the use of heterogeneous catalysis. We have found that functionalized solid materials, e.g., ionic liquids or tin triflates immobilized into mesoporous materials, can be used in N-acylation reactions as environmentally friendly replacements for traditional homogeneous acids which are useful but environmentally unacceptable catalysts [17, 18]. They had comparable activity to homogeneous reagents but can offer greater stability, safer and easier handling and can be... 

Heterogeneous catalysts. In heterogeneous catalysis, the catalyst is in a different phase from the reacting species. Most often, the heterogeneous catalyst is a solid, acting on species in the liquid or gas phase. The solid catalyst can be either of the following. 

In addition, there are a few examples of heterogeneous nonaqueous sonochemistry, in both liquid-liquid and liquid-solid systems. Two recent reports have utilized ultrasonic agitation in place of or along with phase transfer catalysis for the preparation of dichlorocarbene from aqueous NaOH/CHCl3 (166), and for N-alkylation of amines with alkyl halides (167). Along the same lines, several papers have appeared in which... 

The scale of components in complex condensed matter often results in structures having a high surface-area-to-volume ratio. In these systems, interfacial effects can be very important. The interfaces between vapor and condensed phases and between two condensed phases have been well studied over the past four decades. These studies have contributed to technologies from electronic materials and devices, to corrosion passivation, to heterogeneous catalysis. In recent years, the focus has broadened to include the interfaces between vapors, liquids, or solids and self-assembled structures of organic, biological, and polymeric nature. 

Compared with IR and Raman spectroscopies, ultraviolet-visible (UV-Vis) spectroscopy has had only limited use in heterogeneous catalysis. Nevertheless, this spectroscopy can provide information on concentration changes of organic compounds dissolved in a liquid phase in contact with a solid catalyst, be used to characterize adsorbates on catalytic surfaces, provide information on the... 

What we highlight here are some new recent multiphasic reaction systems for catalysis. The systems described here have in common a catalyst-philic phase, which contains, or coats a catalyst (mainly heterogeneous), or in some instances is the catalyst itself (PTC). There are two or three separate phases, and a general composition that can be summarized as liquid-liquid-solid (L-L-S), or liquid-liquid-liquid-solid (L-L-L-S). One of the Ls indicates the liquid-ionic/hydrophilic... 

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