Supported Heteropoly Acids and Multicomponent Polyoxometalates as Eco-Friendly Solid Catalysts for Bulk and Fine Chemicals Synthesis

2013 ◽  
pp. 105-139 ◽  
Author(s):  
G. V. Shanbhag ◽  
Ankur Bordoloi ◽  
Suman Sahoo ◽  
B. M. Devassy ◽  
S. B. Halligudi
ChemInform ◽  
2004 ◽  
Vol 35 (22) ◽  
Author(s):  
Mohamed Zahouily ◽  
Mohamed Salah ◽  
Bouchaib Bahlaouane ◽  
Ahmed Rayadh ◽  
Abdelaziz Houmam ◽  
...  

2021 ◽  
Author(s):  
Zhengqiu Yuan ◽  
Wei Dai ◽  
Shenghong Zhang ◽  
Fengxin Wang ◽  
Jian Jian ◽  
...  

Abstract Lignocellulosic biomass is the most abundant renewable carbon resource on earth, for which many efforts have been made to convert it using various chemocatalytic processes. Heterogeneously chemocatalytic conversion conducted based on reusable solid catalysts is the process with the greatest potential studied presently. This review provides insights into the representative achievements in the research area of heterogeneous chemical catalysis technologies for the production of value-added chemicals from lignocellulosic polysaccharides (cellulose and hemicellulose). Popular approaches for the conversion of lignocellulosic polysaccharides into chemicals, including hydrolyzation (glucose, xylose and arabinose), dehydration (5-hydroxymethylfurfuran, furfural and levulinic acid), hydrogenation/hydrogenolysis (sorbitol, mannitol, xylitol, 1,2-propylene glycol, ethlyene glycol and ethanol), selective oxidation (gluconic acid and lactic acid), have been comprehensively reviewed. However, technological barriers still exist, which have to be overcome to further integrate hydrolysis with the refinery processes based on multifunctional solid catalysts, and convert ligncellulosic polysaccharides into value-added fine chemicals. In general, the approaches and technologies are discussed and critically evaluated in terms of the possibilities and potential for further industrial implementation.


Author(s):  
L. K. Doraiswamy

The use of solid catalysts has a number of advantages compared to catalysis in solution. The most important advantage is their discrete state, usually stationary, which enables easy separation of the product from the catalyst. Although catalysis by solids in organic technology was largely restricted till about the mid-1970s to bulk chemicals produced by continuous processes, it has since been extended to organic intermediates and fine chemicals (which are usually medium to small-volume production in batch processes). We devote this chapter to a brief review of the major types of solid catalysts used in the production of intermediates and fine chemicals. Though these reactions can be carried out in both the vapor and liquid phases, the substrates used in organic synthesis are often relatively complex liquid molecules which tend to decompose under harsh conditions. Hence it is usually desirable to operate under softer conditions, thus preserving the liquid state of the substrate and preventing any likely decomposition to unwanted products. Because catalysis by solids will almost certainly play a major role in organic syntheses of the future, surface science studies involving complex organic molecules are being increasingly undertaken (see, e.g., Rylander, 1979, 1985; Molnar, 1985; Kim and Barteau, 1989; Joyner, 1990; Idriss et al., 1992; Schulz and Cox, 1992, 1993; Pierce and Barteau, 1995; and the recent review by Smith, 1996). However, this book will not be concerned with such mechanistic considerations. There are a few classes of catalysts that have acquired a degree of prominence during the last decade in the synthesis of organic intermediates and fine chemicals that marks them as uniquely relevant in the context of industry’s irreversible shift to green technology. In addition to the homogeneous catalysts considered subsequently in Chapter 9, they include a wide variety of solid catalysts. These catalysts can be classified in two ways: (1) as distinct classes of catalysts that cut across different types of reactions, including dissolved catalysts supported on solids; and (2) as catalysts specific to different types of reactions. It is also possible to control catalytic action by using appropriate solvents/additives.


Tetrahedron ◽  
2004 ◽  
Vol 60 (7) ◽  
pp. 1631-1635 ◽  
Author(s):  
Mohamed Zahouily ◽  
Mohamed Salah ◽  
Bouchaib Bahlaouane ◽  
Ahmed Rayadh ◽  
Abdelaziz Houmam ◽  
...  

2011 ◽  
Vol 84 (3) ◽  
pp. 509-527 ◽  
Author(s):  
Michel Guisnet ◽  
Ludovic Pinard ◽  
Matteo Guidotti ◽  
Federica Zaccheria

The current main concern of global sustainable development pushes toward the substitution of corrosive and highly waste-producing chlorine-containing conventional catalysts (such as the strongly acidic AlCl3–HCl mixture, still widely used in the production of chemicals) by environmentally friendly systems. The outstanding benefits in terms of environmental sustainability as well as of economic advantage related to the use of acid and micro- and/or mesoporous molecular sieves are here depicted, analyzing some selected examples in the field of oil refining, petrochemicals, and fine chemicals production: namely, n-C5–C6 alkane isomerization, isobutane/butene (I/B) alkylation, benzene ethylation, aromatic acylation, and Fries rearrangement. In the large-scale processes of refining and petrochemistry, the shift toward this kind of green and efficient solid catalysts is an established reality. In contrast, in fine chemicals synthesis, most of the novelties are still at a lab-scale level, and additional hurdles, related to the large differences between the national legislations about environmental protection, strongly limit this substitution.


2015 ◽  
Vol 19 (8) ◽  
pp. 681-694 ◽  
Author(s):  
Xian-Dong Lang ◽  
Xiao-Fang Liu ◽  
Liang-Nian He

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