The increased awareness for environmental issues and concomitant environmentally conscious governmental policies has prompted the chemical process industry to implement "greener" production and synthesis methods. In particular, the reduction of the emission of harmful, often organic, substances, reduction of the production of waste, and increasing the energy efficiency are three important aspects in the development of environmentally benign chemical production processes. For the chemical and chemical engineering academic community this has given rise to a new direction, where the concept of "green chemistry" is being explored. Supercritical fluids have been established as promising substitutes to organic solvents. Carbon dioxide is of particular interest as an alternative solvent as it has a low toxicity, is non-flammable and has an accessible critical temperature and pressure. In addition, catalysis is an important tool for the optimization of atom efficiency of a chemical conversion, and therefore for the reduction of waste production. Additionally, catalysis allows for reactions to take place under milder conditions, which can also contribute to an increase in energy efficiency. In particular, soluble molecular organometallic catalysts allow chemical conversions with a higher rate and a better selectivity than their heterogeneous counterparts. The difficult separation of a homogeneous catalyst from reaction products, without deactivating the catalyst, is one of the main obstacles for their application on an industrial scale. Nanofiltration using a microporous ceramic membrane has the potential to be a solution to this problem. A large enough catalyst molecule will be retained while reaction products and solvent can permeate across the membrane. In the field of separation technology membranes have emerged as an energy efficient alternative to conventional separation methods, like distillation and extraction. Ceramic membranes are seen as one of the most promising candidates to purify process streams under demanding conditions. The main objectives of this thesis are the evaluation of the possible advantages of using supercritical carbon dioxide as a solvent as an alternative for organic solvents, and the investigation into the potential of membrane technology for the retention of homogeneous catalysts. The hydroformylation of 1-octene, which is an example of a homogeneously catalyzed reaction on an industrial scale, is considered as a model reaction. To perform the hydroformylation in supercritical carbon dioxide an experimental procedure has been developed, which allows for catalyst preparation under hydroformylation conditions and for carrying out the hydroformylation reaction with a well-defined starting point. It has been demonstrated that with this experimental procedure it is possible to obtain highly reproducible results. Furthermore, a relationship between the change in pressure and the change in reaction mixture composition as a function of time has been established. Using this experimental procedure the effect of total pressure, temperature, concentration of reactants, and concentration of catalyst precursors on the reaction rate, chemoselectivity, and the regioselectivity of the hydroformylation of 1-octene has been studied. The concentration of carbon dioxide had an effect on the regioselectivity of the reaction. Therefore, the same density of solvent has been used for each experiment rather than the more common approach of applying the same total pressure for each experiment. Based on the results obtained by the variation of the reaction parameters a kinetic model has been developed. An optimization method has been applied to find the model parameter values that best describe the experimental data. The observed kinetics for the catalyst based on rhodium(I) dicarbonyl acetylacetonate and tris(3,5-bis(trifluoromethyl)phenyl)phosphine shows resemblance to that observed for the hydroformylation where bulky phosphites have been used as the ligand. For this catalyst a high activity in the order of 5×103 to 12×103 mol1-octene molRh-1 h-1 has been observed at 70 °C. Organometallic complexes based on rhodium with phosphine ligands with a varying number of trifluoromethyl groups have been screened for their activity and selectivity for the hydroformylation of 1-octene. Furthermore, the effect of the type of solvent: carbon dioxide, hexane, and toluene has been included in this study. An increase in the number of trifluoromethyl substituents on the triphenylphosphine ligand results in an increase in 1-octene conversion rate and a decrease in the overall selectivity towards aldehydes. This behaviour is observed in all three solvents. For supercritical carbon dioxide or hexane, as the solvent, the outcome of the hydroformylation reaction in terms of activity and selectivity shows great similarity. By following the hydroformylation of 1-octene in time, it was observed that during batch operation rhodium catalysts with trifluoromethyl-substituted triarylphosphines showed a higher differential regioselectivity than based on the overall regioselectivity at the end of the reaction. For the hydroformylation in carbon dioxide this effect was most pronounced. Both the mode of operation, batch or semi batch, and the type of solvent had a significant influence on this phenomenon. The transport of a supercritical fluid across a microporous alumina supported titania membrane has been investigated. The dependence of the permeation of carbon dioxide across the titania membrane on the feed pressure is similar to what has been previously observed for microporous alumina supported silica membranes. At high feed pressure viscous flow appears to be the main mechanism of mass transport across the membrane. Furthermore, the titania membrane shows a reasonable stability over a period of operation of about at least six months in varying conditions. Finally, the first continuously operated experiment has been performed, in which hydroformylation of 1-octene and separation of the catalyst have been integrated using a membrane reactor. During a 27.5 h of operation of the membrane reactor, spread over four consecutive days, a maximum conversion of 17 % and a maximum regioselectivity of 5 in terms of n:iso ratio has been observed. The conversion and the n:iso ratio, which is the ratio between the linear and branched aldehyde product, decrease as a function of the number of permeated reactor volumes indicating a loss of catalyst. Permeation of free ligand and the catalytic species through the membrane appear to be the main reasons for the decrease in activity and selectivity. A good match between membrane retention characteristics and the size of the catalyst and its precursors is not found yet. However, a number of feasible improvements can be made to improve the retention of the catalyst. Using a membrane for retention of a homogeneous catalyst in combination with the application of carbon dioxide as a solvent for the continuous hydroformylation of 1-octene has great potential. Successful application of the envisioned membrane reactor process can have implications for other homogeneously catalyzed reactions of which asymmetric hydrogenation is a commercially relevant example. As a result of the experimental methods used in this thesis the potential benefits of using carbon dioxide as an environmentally benign alternative to organic solvents could be further extended.