Disperse soluble immobilized

Because enzymes are insoluble in organic solvent, mass-transfer limitations apply as with any heterogeneous catalyst. Water-soluble enzymes (which represent the majority of enzymes currently used in biocatalysis) have hydrophilic surfaces and so tend to form aggregates or stick to reaction vessel walls rather than form the fine dispersions that are required for optimum efficiency. This can be overcome by enzyme immobilization, as discussed in Section 1.5. 

Catalytically active particles can be formed from various palladium sources under supercritical reaction condition, which could be helpful for the particle dispersion. Therefore, those materials show high catalytic activity, selectivity, and stability for a broad range of substrates. Additionally, the PEG matrix effectively stabilizes and immobilizes the catalytically active particles, whereas the unique solubility and mass transfer properties of scC02 allow continuous processing at mild conditions, even with low-volatility substrates. 

The area of catalyst immobilization has received considerable attention as can be judged from the available literature reviews.[1 30] Immobilization of oxidation catalysts shows intrinsic advantages over other catalysts as the tendency for selfoxidation will decrease. Moreover, complexes with generally low solubility, such as heme-type transition metal complexes, can be dispersed molecularly on supports. It is the aim of the present work to overview the state of knowledge on the immobilization of transition metal complexes using microporous supports, such as zeolites and laminar supports like clays. The wealth of information available for complexes immobilized on LDHs or tethered to the mesopore walls in hierarchically organized oxides will not be dealt with. 

Partial silylation of the highly disperse silica surface enhances the adsorption of vitamin E from ethanol solution, and provides the ability to obtain water-soluble nanocomposites containing vitamin E. Immobilization of vitamin C on the silica surface prevents its oxidation. Its interaction with the adsorbent surface leads to a decrease in proton-donor ability of the OH-groups involved in the oxidation of ascorbic acid. Elydrophobized silica nanocomposites are characterized by a prolonged desorption of immobilized vitamins. It has been shown that vitamin C does not lose its antioxidant properties after desorption. 

These findings indicate that even though the lime stabilization process of the biosolid waste may contribute to increased immobilization of soluble metals by sorption or precipitation onto the solid phase, in retrospect, it could create conditions favorable for increased dispersion and mobility of colloid particles and their metal load. 

Inorganic contaminants are immobilized by washing the waste with soluble phosphates. This treatment uses a very small amount of phosphate, does not change other characteristics of the waste such as its granular nature or volume, and is relatively inexpensive. If the waste contains radioactive contaminants, phosphate washing is not sufficient because the dispersibility of the radioactive contaminant powders needs to be reduced, and hence, the waste needs to be solidified. Solidification requires generating phosphate ceramics of the waste in the form of a CBPC. In the case of radioactive waste, both stabilization and solidification are needed because they not only immobilize the contaminants, but also solidify the entire waste. As we will see in this and the next chapter, whether phosphate treatment is used only for stabilization or for both stabilization and solidification, it is very effective for a wide range of waste streams. 

The prospect of using enzymes as heterogeneous catalysts in scC02 media has created significant interest. Their low viscosity and high diffusion rates offer the possibility of increasing the rate of mass-transfer controlled reactions. Also, because enzymes are not soluble in supercritical fluids, dispersion of the free enzymes potentially allows simple separations without the need for immobilization. 

The microsealed delivery device is a variation of the matrix-type transdermal system in which the drug is dispersed in a reservoir phase which is then immobilized as discrete droplets in a cross-linked polymeric matrix. Release can be further controlled by inclusion of a polymeric microporous membrane. This system therefore combines the principles of both the liquid reservoir and matrix-type devices. Rate of release of a drug from a microsealed delivery system is dependent on the partition coefficient between the reservoir droplets and the polymeric matrix the diffusivity of the drug in the reservoir, the matrix and the controlling membrane and on the solubility of the drug in the various phases. There are, obviously, many ways to achieve the desired zero-order release rate, but only nitroglycerin has been commercially formulated into this type of delivery device (Karim 1983). 

Phthalocyanine (Pc) complexes of transition metals have received much attention in the scientific literature of the last two decades, not only as mild catalysts for selective oxidation reactions but also as functional models for enzymes. Unfortunately, their use is hampered by their reduced solubility in solvents and their tendency to form adducts even when used in solution. Provided such complexes can be immobilized individually on a catalyst carrier, it is expected that an enhanced dispersion of the complex will be achieved. The use of heterogenized Pc complexes will also no longer be restricted by the nature of the reaction medium or solvent. The issue has been reviewed as early as 1986 [3]. 

Because enzymes are not soluble in SCFs it should be possible to disperse free enzyme in the SCF and recover the enzyme without the need to immobilize it on a support. 

CDs are equably dispersed in polymer. A kind of soluble polymers (polyvinyl acetate, PAM) is chosen and dissolved in solvents (acetone, ethyl acetate). Then CD is added and scattered in the solvents. Finally, the solvent is evaporated and the CDP blend is prepared. It is the gentlest CD immobilization method, as it is not a chemical reaction, and is widely used as the operation is simple. For example, the polymer blend of CD/polyacrylamide can be used as filling materials of capillary chromatographic column. Its separation efficiency is as high as 10,000 layer/15 cm. If spices or fungicide are added to CD before blending with polyethylene, the blend products can be used as flavor enhancer or antibacterial packaging material. 

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