Rotating bed reactor packed with heterofunctional structured silica-supported lipase. Developing an effective system for the organic solvent and aqueous phase reactions

2021 ◽  
Vol 312 ◽  
pp. 110789
Author(s):  
Daria Kowalczykiewicz ◽  
Katarzyna Szymańska ◽  
Danuta Gillner ◽  
Andrzej B. Jarzębski
1984 ◽  
Vol 32 (10) ◽  
pp. 1107-1112 ◽  
Author(s):  
E T Mays ◽  
R C Feldhoff ◽  
G S Nettleton

In phase partition fixation tissue is immersed in an organic solvent at equilibrium with an aqueous phase containing a fixing agent. By using radioisotope labeling techniques the effects of phase partition fixation on protein retention during fixation of tissue with formalin and glutaraldehyde have been determined and compared with those of standard aqueous fixation using these fixatives. It has been shown that retention of protein in tissue during phase partition fixation was as good or better than during aqueous fixation. Improved retention provides further evidence that phase partition fixation may be a useful alternative to aqueous fixation.


1982 ◽  
Vol 47 (11) ◽  
pp. 2904-2911 ◽  
Author(s):  
Jaroslav Šilhánek ◽  
Lenka Konrádová ◽  
Olga Šimečková ◽  
Josef Horák

The rate of hydrolysis was studied for triphenylmethyl chloride in water-organic solvent systems with an unstirred interface of a known area. The hydrolytic reaction was found to take place at the interface only. The temperature dependence of the reaction rate indicates that at lower temperatures (up to 60 °C) the rate-determining step is the chemical reaction, whereas at higher temperatures a deviation from the Arrhenius type dependence is observed, which along with the low activation energy value points to the diffusion as the governing phenomenon. The effect of salts added to the aqueous phase is consistent with the expected behaviour for the SN1 mechanism, but suprising is the inhibiting effect od some quaternary ammonium salts. In the study of the effect of the organic solvent, the reaction rate was found to correlate satisfactorily with the solubility of the organic solvent in water, but no correlation was established with the solubility of water in the solvent. From the results obtained it can be inferred that the reaction site is the laminary layer adjacent to the interface from the aqueous phase side.


1995 ◽  
Vol 44 (4) ◽  
pp. 307-309 ◽  
Author(s):  
Shigeru TAGUCHI ◽  
Tomoko GOKI ◽  
Noriko HATA ◽  
Issei KASAHARA ◽  
Katsumi GOTO

Author(s):  
L. K. Doraiswamy

The chemical equilibria of many industrially important organic reactions in aqueous solutions are often displaced in the direction of the reactants, leading to very low conversions. Therefore, there is a need for an environmentally friendly strategy that will shift the equilibria toward the products, resulting in enhanced conversions. A particularly effective technique is to add a second phase, appropriately termed biphasing. In general, biphasing is the intentional addition of an immiscible phase to a reaction mixture to increase the yield of the desired product or to facilitate separation of product from (say) catalyst. Much of the effort till recently has been on adding a water-immiscible organic solvent in enzyme-catalyzed organic reactions in the aqueous phase. Although strictly the term biphasing should apply only to soluble catalysts, thus preserving the purity of its definition, in practice it also includes insoluble catalysts such as immobilized enzymes (which would constitute a third phase). Biphasing received an exciting stimulus around 1984 when it was used to overcome the inherent and perhaps the most telling deficiency of homogeneous catalysis. By biphasing with an aqueous phase (unlike in enzymatic catalysis where the biphasing liquid is an organic solvent), the catalyst was fully retained in that phase, whereas the product (and unused reactant) remained in the organic phase. The consequent easy separation of catalyst from product added a new dimension to homogeneous catalysis that gives it a decided edge over its heterogeneous counterpart for many reactions. Yet another dimension to biphasing was added in the last decade when it was found that both phases could be aqueous. This variant of traditional biphasing has many obvious advantages. Although still in its infancy, its enormous potential is not difficult to visualize. The chief advantages and disadvantages of biphasing are listed in Table 18.1. We begin our treatment of biphasing by developing the theoretical foundation for predicting an apparent or effective equilibrium constant for a biphasic reaction. This will be done specifically for enzyme-catalyzed reactions, but it can be extended to straight organic synthesis. Several important aspects of these biphasic systems, such as solvent selection and the role of mass transfer, will be discussed.


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