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Sugar hydrogenation

For small catalyst particles used in sugar hydrogenation (slurry reactors), one would intuitively conclude that the system is safely within the kinetic regime. [Pg.179]

We have presented a general reaction-diffusion model for porous catalyst particles in stirred semibatch reactors applied to three-phase processes. The model was solved numerically for small and large catalyst particles to elucidate the role of internal and external mass transfer limitations. The case studies (citral and sugar hydrogenation) revealed that both internal and external resistances can considerably affect the rate and selectivity of the process. In order to obtain the best possible performance of industrial reactors, it is necessary to use this kind of simulation approach, which helps to optimize the process parameters, such as temperature, hydrogen pressure, catalyst particle size and the stirring conditions. [Pg.194]

Avoid desserts, ice cream, and meat alternatives made from soy. These products usually include acidic ingredients such as sugar, hydrogenated fats, or wheat gluten. [Pg.94]

The principal structural difference between DNA and RNA is the 2 OH group of ribose in RNA molecules. In DNA, which lacks the 2 OH group in the deoxyribose sugar, hydrogen-bonded complementary strands can easily adopt the B-form double helix. In contrast, double-stranded regions of RNA molecules cannot adopt this conformation because of steric hindrance. Instead, they adopt the less compact A-helical form in which there are 11 bp per turn and the base pairs tilt 20° away from the horizontal. [Pg.731]

A glycoprotein is a protein with covalently attached sugars. Hydrogen bonding maintains the secondary structure of a protein and contributes to the stability of the tertiary and quaternary levels of structure. [Pg.835]

The specific example of sugar hydrogenation (e. g. glucose to sorbitol) has warranted an individual chapter in this book and so is excluded here. Reference to enantioselective hydrogenation of pro-chiral ketones is only included where appropriate, for the same reason. [Pg.363]

It is also worth mentioning that we were able to carry out these reactions at 50 bars of pressure in which is more characteristic of a slurry phase reaction with a powder catalyst (19) than the pressures of 150 to 400 bar as given in the literature for fixed bed sugar hydrogenations (7, 20, 21, 22). Such an improvement in the operating pressure of this reaction should lead to sizeable savings in its operation. [Pg.295]

Raney nickel and supported nickel catalysts are currently used for almost all sugar hydrogenation processes. Typical glucose hydrogenation reaction conditions for batch, slurry and continuous, fixed bed catalytic processes are... [Pg.6]

Ruthenium catalysts cannot compete with nickel catalysts for sugar hydrogenation on a direct comparison of catalyst cost contribution because of the difference in metal value. However, environmental legislation and the increasing cost of waste disposal and waste water treatment is changing the situation and presenting opportunities for ruthenium catalysts for the future. [Pg.7]

Fig. 8. View of the structure of 8-azaadenosine (Reference 18). The sugar hydrogen atoms have... Fig. 8. View of the structure of 8-azaadenosine (Reference 18). The sugar hydrogen atoms have...
In diis chapter, the main technical aspects of different thermochemical processes for biomass conversion are discussed. In addition, various hydro-thermal treatments applied to lignocellulosic biomass for the production of fermentable sugars, hydrogen or other value-added products are presented. This chapter also describes about pyrolysis along with its various parameters that influence conversion product yields. Bio-oil, which is a complex mixture or both aqueous and organic biomass components, is discussed in details along with its catalytic upgrading for use as transportation fuel. [Pg.329]

From Figure 11.9, it can be seen that alcohols are produced from biomass in the conversion pathway sequence of ammonia explosion, organosolv separation, dehydration of sugars, hydrogenation of furfural and hydrogenation of TUFA 1. Alkane,- is produced from fractional distillation of alkanes, which are produced from pyrolysis of biomass, followed by Fischer-Tropsch process 2 together with dehydration of alcohols 2. The selected conversion pathways consist of both biochemical and thermochemical pathways. The comparison of the results generated for scenario 1 and 2 is summarised in Table 11.13. [Pg.294]

Industrial production is based on 50% solutions of D-glucose (dextrose). The yield of s. depends strictly on the purity of the sugar. Hydrogenation is performed continuously under high pressure on fixed-bed Cu-oxide or Ni-oxide catalysts. After refining, the reaction fluid is evaporated to 70% d.s. (main commercial product). S. powder may be prepared by (spray)crystallization of highest-purity s. [Pg.261]


See other pages where Sugar hydrogenation is mentioned: [Pg.168]    [Pg.171]    [Pg.173]    [Pg.180]    [Pg.180]    [Pg.518]    [Pg.193]    [Pg.193]    [Pg.233]    [Pg.233]    [Pg.452]    [Pg.810]    [Pg.811]    [Pg.173]    [Pg.413]    [Pg.426]    [Pg.428]    [Pg.272]    [Pg.99]    [Pg.54]    [Pg.109]    [Pg.152]    [Pg.447]    [Pg.1]    [Pg.17]    [Pg.20]    [Pg.140]   
See also in sourсe #XX -- [ Pg.109 ]




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