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Other Solid Bases

Pure basic oxide (alkaline and alkaline-earth oxides) are also used industrially, but due to the difficulty in obtaining thermally-stable materials with high surface area [Pg.154]

For this reason, recent attention has been dedicated to micro- and meso-porous materials (MMM), and also for their possible use as shape-selectivity controlled reactions (space-restricted transition states, preferential diffusion and back-diffusion). Even if the latter aspects are better known regarding the performances of microporous materials, other aspects can be evidenced. In fact, also in mesoporous materials, where the dimensions of the channels are larger, as required for shape-selectivity effects, a change of reactivity of molecules inside the channels could be present due to confinement effects [281]. Therefore, the catalytic reactivity shown by basic sites located inside mesoporous channels could differ from that of the same sites located instead on the external surface of the mesoporous ordered material. [Pg.155]

There are basically two options in the purification, that is, the water washing process and adsorbent treatment process (water-free process). In the water washing process the main drawbacks are the amount of wastewater produced and the energy costs to evaporate and recover water for re-use. In the adsorbent treatment process the problems are the high cost of adsorbent (e.g., Mg-silicate) and the disposal of the spent adsorbents. A potential cleaner process should thus eliminate the catalyst cleanup step and simplify biodiesel and glycerol purification. The options are (i) the use of heterogeneous solid catalysts, (ii) the use of an enzymatic transesterification processes and (iii) a catalyst-free process, using, for example, supercritical methanol. [Pg.156]

Enzymatic transesterification is under investigation [287, 288], but the cost of lipase production is the main hurdle for commercialization. Intracellular lipase as a vhole cell biocatalyst could lo ver the lipase production cost. Another problem is ho v to maintain lipase activity in the presence of a high concentration of methanol and glycerol. Industrialization is under investigation, but still not realized. [Pg.157]

Transesterification using supercritical methanol is also possible [289-291]. No catalyst is needed and in 5 min over 90% conversion could be reached. Hovv ever, high temperatures (350 °C) and pressures (45 MPa) are necessary, as vell as a high methanol to oil ratio ( 40). The advantage is that free fatty acids in crude oils and fats could also be converted into methyl esters. Hovv ever, the main limitations are the high investment and energy costs, and the use of excessive methanol. There are good advances to overcome these limits, but the industrialization is still far. [Pg.157]


Addition of water (36) or alcohols (37—39) direcdy to butadiene at 40—100°C produces the corresponding unsaturated alcohols or ethers. Acidic ion exchangers have been used to catalyze these reactions. The yields for these latter reactions are generally very low because of unfavorable thermodynamics. At 50°C addition of acetic acid to butadiene produces the expected butenyl acetate with 60—100% selectivity at butadiene conversions of 50%. The catalysts are ion-exchange resins modified with quaternary ammonium, quaternary phosphonium, and ammonium substituted ferrocenyl ions (40). Addition of amines yields unsaturated alkyl amines. The reaction can be catalyzed by homogeneous catalysts such as Rh[P(C(5H5)3]3Q (41) or heterogeneous catalysts such as MgO and other solid bases (42). [Pg.342]

The Tishchenko reaction of furfural has been found to be difficult when carried out by traditional homogeneous catalysis, but excellent results for the Tishchenko reaction of furfural and 3-furaldehyde[90,91] using CaO and SrO as catalysts have been obtained. The use of other solid base catalysts such as La203, Zr02, ZnO, 7-alum in a, hydrotalcite and KOH/alumina, was unsuccessful. An investigation of the influence of the pretreatment temperature of the MgO and CaO catalysts showed that the active basic sites for this transformation are not OH groups, but rather O2 ions on the MgO surface. [Pg.183]

However, the second step requires stronger basic sites than the first step. This demonstrates the importance of being able to tune the base strength. In this sense, zeolites form a valuable complement to other solid base catalysts, e.g. MgO, or mixed oxides derived from layered double hydroxides. [Pg.269]

The FBA reactor design is probably the most peculiar feature of the process, as compared to other solid-based alkylation technologies. The reactor is of fixed bed type, being filled with pellets of the porous support. The supported liquid acid phase is not homogeneously distributed along the reactor bed instead, the acid liquid is confined to a certain so-called reaction zone, which slowly moves downward in the hydrocarbons flow direction, though at a much slower rate. According to the known chemistry for the liquid acid catalyzed alkylation, the ester... [Pg.140]

Solid oxide fuel cells consist of solid electrolytes held between metallic or oxide elecU odes. The most successful fuel cell utilizing an oxide electrolyte to date employs Zr02 containing a few mole per cent of yttrium oxide, which operates in tire temperature range 1100-1300 K. Other electrolytes based... [Pg.244]

But the diagram shows another feature which looks like a eutectic it is the V at the bottom of the austenite field. The transformation which occurs there is very like the eutectic transformation, but this time it is a solid, austenite, which transforms on cooling to two other solids. The point at the base of the V is called a eutectoid point. [Pg.356]

Note that these mechanisms are the reverse of those involved in the acid-catalyzed hydration of double bonds (15-3), in accord with the principle of microscopic reversibility. With anhydrides (e.g., P2O5, phthalic anhydride) as well as with some other reagents such as HMPA, it is likely that an ester is formed, and the leaving group is the conjugate base of the corresponding acid. In these cases, the mechanism can be El or E2. The mechanism with AI2O3 and other solid catalysts has been studied extensively but is poorly understood. [Pg.1328]

The other main support used for solid base catalysts is polystyrene, which while it does not have a well-defined porous structure, does swell in solvents providing an accessible high surface area on which to carry out reactions. One common method of chemically attaching groups to polystyrene involves incorporation of specific amounts of styrene contain-... [Pg.101]

What makes metal nanoclusters scientifically so interesting The answer is that they, in many respects, no longer follow classical physical laws as all bulk materials do, but are correctly to be considered by means of quantum mechanics. This is not only valid for metals. In principle any other solid or in some cases even liquid material exhibit so-called nano-effects when reaching a critical size. Nanoscience and nanotechnology are based on those effects. In the course of only 1-2 decades nanosciences and nanotechnology have developed to such an extent that our daily life already is and will be increasingly influenced in a way that cannot be compared with any other technological development in mankind s history [2]. A few examples will help to better understand what is meant. [Pg.3]

Solid Acid Catalysed Esterification of Amino Acids and Other Bio-Based Acids... [Pg.373]

For more efficient utilization of MOFs sorbents, several hybrid systems based on MOFs with other solid sorbents have been investigated in the literature. The objective of having hybrid materials is to utilize the synergism between the two sorbents and therefore ultimately improve the overall performance in C02 separation. Moreover, sorbents such as activated carbons, graphenes, and CNTs provide the added feature of high surface area and easily functionalized sites which contribute to the tuning of the final properties of the composite... [Pg.136]

The solid base decomposes violently in contact with cone. acid. See other high-nitrogen compounds, organic bases... [Pg.274]

E. coli, Bacillus and Pseudomonas present quite a solid base for the production of non-glycosylated proteins. Nevertheless, a number of other prokaryotic expression hosts exist that are not as well established and which show features that are not present in the major expression organisms, and this could be extremely useful for special case proteins. [Pg.43]

Lemli and Knockaert [33] described a spectrophotometric method for the determination of miconazole nitrate suspensions and other organic bases in pharmaceutical preparations by the use of cobalt thiocyanate. The drug and the amines (as their anhydrous hydrochlorides in dichloromethane) react with solid cobalt thiocyanate to form an ion-pair complex that contains two molecules of base to one [Co(SCN)4]2. The complex is determined quantitatively by spectrophotometry versus dichloromethane at 625 nm with rectilinear response for up to 400 pg/mL of the base. This method was applied to miconazole nitrate suspensions and the coefficient of variations were generally <2%. [Pg.41]

Liquid-solid distributions are involved in ion-exchange and other adsorption-based separation processes, separation processes based on crystallization or precipitation, flotation processes for ore dressing, and smelting processes. [Pg.760]

Not all colloid systems are stable. The most stable involve solid dispersion media, since movement through a solid host will be slow. Emulsions also tend to be stable think, for example, about a glass of milk, which is more likely to decompose than undergo the destructive process of phase separation. Aerosols are not very stable although a water-based polish generates a liquid-in-air colloid, the particles of liquid soon descend through the air to form a pool of liquid on the table top. Smoke and other solid-in-gas aerosols are never permanent owing to differences in density between air and the dispersed phase. [Pg.508]


See other pages where Other Solid Bases is mentioned: [Pg.270]    [Pg.272]    [Pg.88]    [Pg.362]    [Pg.154]    [Pg.154]    [Pg.52]    [Pg.46]    [Pg.270]    [Pg.272]    [Pg.88]    [Pg.362]    [Pg.154]    [Pg.154]    [Pg.52]    [Pg.46]    [Pg.560]    [Pg.102]    [Pg.294]    [Pg.898]    [Pg.377]    [Pg.441]    [Pg.588]    [Pg.541]    [Pg.145]    [Pg.39]    [Pg.13]    [Pg.178]    [Pg.470]    [Pg.394]    [Pg.327]    [Pg.81]    [Pg.198]    [Pg.59]    [Pg.500]    [Pg.132]    [Pg.5]    [Pg.295]    [Pg.22]   


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