During this PhD thesis, cobalt (Co) catalysts have been prepared, characterized and studied in the carbon monoxide hydrogenation (CO+H2) reaction (also known as “Fischer-Tropsch” (FT) reaction). In industry, the FT synthesis aims at producing long chain hydrocarbons such as gasoline or diesel fuels. The interest is that the reactants (CO and H2) are obtained from other carbonaceous sources than crude oil: natural gas, coal, biomass or even petroleum residues. As it is well known that the worldwide crude oil reserves will be depleted in a few decades, the FT reaction represents an attractive alternative for the production of various fuels. Moreover, this reaction can also be used to produce high value specialty chemicals (long chain alcohols, light olefins…). Two different types of catalysts have been investigated during this thesis: cobalt with magnesia used as support or dispersant (Co/MgO) and cobalt with silica used as support (Co/SiO2). Each catalyst from the first class is prepared by precipitation of a mixed Co/Mg oxalate in acetone. This coprecipitation is followed by a thermal decomposition under reductive atmosphere leading to a mixed Co/MgO catalyst. On the other hand, Co/SiO2 catalysts are prepared by impregnation of a commercial silica support with a chloroform solution containing Co nanoparticles. This impregnation is then followed by a thermal activation under reductive atmosphere. The mixed Co/Mg oxalates and the resulting Co/MgO catalysts have been extensively characterized in order to gain a better understanding of the composition, the structure and the morphology of these materials: thermal treatments under reductive and inert atmospheres (followed by MS, DRIFTS, TGA and DTA), BET surface area measurements, XRD and electron microscopy studies have been performed. Moreover, an original in situ technique for measuring the H2 chemisorption surface area of catalysts has been developed and used over our catalysts. The performances of the Co/MgO and Co/SiO2 catalysts have then been evaluated in the CO+H2 reaction at atmospheric pressure. Chemical Transient Kinetics (CTK) experiments have been carried out in order to obtain information about the reaction kinetics and mechanism and the nature of the catalyst active surface under reaction conditions. The influence of several experimental parameters (temperature, H2 and CO partial pressures, total volumetric flow rate) and the effect of passivation are also discussed with regard to the catalyst behavior. Our results indicate that the FT active surface of Co/MgO 10/1 (molar ratio) is entirely covered by carbon, oxygen and hydrogen atoms, most probably associated as surface complexes (possibly formate species). Thus, this active surface does not present the properties of a metallic Co surface (this has been proved by performing original experiments consisting in switching from the CO+H2 reaction to the propane hydrogenolysis reaction (C3H8+H2) which is sensitive to the metallic nature of the catalyst). CTK experiments have also shown that gaseous CO is the monomer responsible for chain lengthening in the FT reaction (and not any CHx surface intermediates as commonly believed). Moreover, CO chemisorption has been found to be irreversible under reaction conditions. The CTK results obtained over Co/SiO2 are quite different and do not permit to draw sharp conclusions concerning the FT reaction mechanism. More detailed studies would have to be carried out over these samples. Finally, Co/MgO catalysts have also been studied on a combined DRIFTS/MS experimental set-up in Belfast. CTK and Steady-State Isotopic Transient Kinetic Analysis (SSITKA) experiments have been carried out. While formate and methylene (CH2) groups have been detected by DRIFTS during the FT reaction, the results indicate that these species play no role as active intermediates. These formates are most probably located on MgO or at the Co/MgO interface, while methylene groups stand for skeleton CH2 in either hydrocarbon or carboxylate. Unfortunately, formate/methylene species have not been detected by DRIFTS over pure Co catalyst without MgO, because of the full signal absorption.

Reaction water, a high-strength COD (chemical oxygen demand) petrochemical effluent, is generated during the Fischer-Tropsch reaction in the SASOL Synthol process at SASOL SynFuels, Secunda, South Africa. Distillation of the reaction water to remove non- and oxygenated hydrocarbons yields approximately 25 - 30 ML/d of an organic (carboxylic) acid-enriched stream (average COD of 16 000 mg/L) containing primarily C2 – C5 organic acids, light oils, aldehydes, ketones, cresols and phenols. Together with the Oily sewer water (API) and Stripped Gas Liquor (SGL) process streams, this process effluent is currently treated in ten dedicated activated sludge basins. However, the successful operation of these activated sludge systems has proven to be difficult with low organic loading rates (3.5 kg COD/m3.d) low COD removal efficiencies (<80 %) and high specific air requirements (60 - 75 m3 air/kg CODrem). It is hypothesised that these operational difficulties can be attributed to organic shock loadings, variation in volumetric and hydraulic loadings, as well as variations in the composition of the various process streams being treated. Due to the fact that the Fischer-Tropsch (Synthol) reaction water constitutes 70 % of the COD load on the activated sludge systems, alternative processes to improve the treatment cost and efficiency of the Fischer-Tropsch acid stream are being investigated. Various studies evaluating the aerobic and anaerobic treatment of Fischer-Tropsch reaction water alone in suspended growth wastewater treatment systems have proven unsuccessful. High rate fixed-film processes or biofilm reactors, of which the fluidised-bed reactors are considered to he one of the most effective and promising processes for the treatment of high-strength industrial wastewaters, could he a suitable alternative. The primary aim of this study was to evaluate the suitability of biological fluidised-bed reactors (BFBRs) for the treatment of Fischer-Tropsch reaction water. During this study, the use of aerobic and anaerobic biological fluidised-bed reactors (BFBR), using sand and granular activated carbon (GAC) as support matrices, were evaluated for the treatment of a synthetic effluent analogous to the Fischer-Tropsch reaction water stream. After inoculation, the reactors were operated in batch mode for 10 days at a bed height expansion of 30% and a temperature of 30 ºC to facilitate biofilm formation on the various support matrices. This was followed by continuous operation of the reactors at hydraulic retention times (HRTs) of 2 days. While the COD of the influent and subsequent organic loading rate (OLR) was incrementally increased from 1 600 mg/L to a maximum of 20 000 mg/L and 18 000 mg/L for the aerobic and anaerobic reactors, respectively. Once the maximum influent COD concentration had been achieved the OLR was further increased by decreasing the HRTs of the aerobic and anaerobic reactors to 24h and 8h, and 36h, 24h and 19h, respectively. The dissolved O2 concentration in the main reactor columns of the aerobic reactors was constantly maintained at 0.50 mg/L. Chemical Oxygen Demand (COD) removal efficiencies in excess of 80 % at OLR of up to 30 kg COD/m3.d were achieved in the aerobic BFBRs using both sand and GAC as support matrices. Specific air requirements were calculated to be approximately 35 and 41 m3 air/kg CODrem for the BFBRs using sand and GAC as support matrices, respectively. The oxygen transfer efficiency was calculated to be approximately 5.4 %. At high OLR (> 15 kg COD/m3.d) significant problems were experienced with plugging and subsequent channelling in the BFBR using GAC as support matrix and the reactor had to be backwashed frequently in order to remove excess biomass. Despite these backwash procedures, COD removal efficiencies recovered to previous levels within 24 hours. In contrast, no significant problems were encountered with plug formation and channelling in the BFBR using sand as support matrix. In general the overall reactor performance and COD removal efficiency of the aerobic BFBR using sand as support matrix was more stable and consistent than the BFBR using GAC as support matrix. This BFBR was also more resilient to variations in operational conditions, such as the lowering of the hydraulic retention times and changes in the influent pH. Both aerobic reactors displayed high resilience and COD removal efficiencies in excess of 80 % were achieved during shock loadings. However, both reactors were highly sensitive to changes in pH and any decrease in pH below the pKa values of the volatile fatty acids in the influent (pKa of acetic acid = 4.76) resulted in significant reductions in COD removal efficiencies. Maintenance of reactor pH above 5.0 was thus an essential facet of reactor operation. It has been reported that the VFA/alkalinity ratio can be used to assess the stability of biological reactors. The VFA/alkalinity ratios of the aerobic BFBRs containing sand and GAC as support matrices were stable (VFNalkalinity ratios of < 0.3 - 0.4) until the OLR increased above 10 kg/m3.d. At OLRs higher than 10 kg/m3.d the VFA/alkalinity ratios in the BFBR using sand support matrix increased to 4, above the failure limit value of 0.3 - 0.4. In contrast the VFA/alkalinity ratios of the BFBR using GAC support matrix remained stable until an OLR of 15 kg/m3.d was obtained, where the VFA/alkalinity ratios then increased to > 3. Towards the end of the study when an OLR of approximately 25 kg/m3.d was obtained the VFA/alkalinity ratios of both the BFBRs using sand and GAC as support matrices increased to 9 and 6 respectively, indicating the decrease in reactor stability and acidification of the process. Total solid (TS) and volatile solid (VS) concentrations in the aerobic BFBRs were initially high and decreased over time. While the total suspended solids (TSS) and volatile suspended solids (VSS) concentrations were initially low and increased over time as the OLR was increased, this is thought to be as a result of decreased HRT leading to biomass washout. The anaerobic BFBR using sand as support matrix never stabilised and COD removal efficiency remained very low (< 30 %), possibly due to the high levels of shear forces. Further studies concerning the use of sand as support matrix were subsequently terminated. An average COD removal efficiency of approximately 60 % was achieved in the anaerobic BFBR using GAC as a support matrix at organic loading rates lower than 10 kg COD/m3.d. The removal efficiency gradually decreased to 50 % as organic loading rates were increased to 20 kg COD/m3.d. At OLRs of 20 kg COD/m3.d, the biogas and methane yields of the anaerobic BFBR using GAC as support matrix were determined to be approximately 0.38 m3 biogas/kg CODrem (0.3 m3 biogas/m3reactor vol.d), and 0.20 m3 CH4/kg CODrem (0.23 m3 CH4/m3reactor vol.d), respectively. This value is 57 % of the theoretical maximum methane yield attainable (3.5 m3 CH4/kg CODrem). The methane yield increased as the OLR increased, however, when the OLR reached 8 kg/m3.d the methane yield levelled off and remained constant at approximately 2 m3 CH4/m3reactor vol.d. Although the methane content of the biogas was initially very low (< 30 %), the methane content gradually increased to 60 % at OLRs of 20 kg COD/m3.d. The anaerobic BFBR using GAC as support matrix determined that as the OLR increased (>12 kg/m3.d), the VFA/alkalinity ratio increased to approximately 5, this is indicative of the decrease in stability and acidification of the process. The anaerobic BFBR using GAC as support matrix experienced no problems with plug formation and channelling. This is due to the lower biomass production by anaerobic microorganisms than in the aerobic reactors. The TS and VS concentrations were lower than the aerobic concentrations but followed the same trend of decreasing over time, while the TSS and VSS concentrations increased due to decreased HRTs. The anaerobic BFBR was sensitive to dramatic variations in organic loading rates, pH and COD removal efficiencies decreased significantly after any shock loadings. Compared to the activated sludge systems currently being used for the biological treatment of Fischer-Tropsch reaction water at SASOL SynFuels, Secunda, South Africa, a seven-fold increase in OLR and a 55 % reduction in the specific air requirement was achieved using the aerobic BFBRs. The methane produced could also be used as an alternative source of energy. It is, however, evident that the support matrix has a significant influence on reactor performance. Excellent results were achieved using sand and GAC as support matrices in the aerobic and anaerobic BFBRs, respectively. It is thus recommended that future research be conducted on the optimisation of the use of aerobic and anaerobic BFBRs using these support matrices. Based on the results obtained from this study, it can be concluded that both aerobic and anaerobic treatment of a synthetic effluent analogous to the Fischer-Tropsch reaction water as generated by SASOL in the Fischer-Tropsch Synthol process were successful and that the application of fluidised-bed reactors (attached growth systems) could serve as a feasible alternative technology when compared to the current activated sludge treatment systems (suspended growth) currently used. Keywords: aerobic treatment, anaerobic treatment, biological fluidised-bed reactors, petrochemical effluent, Fischer-Tropsch reaction water, industrial wastewater. / Thesis (M. Omgewingswetenskappe)--North-West University, Potchefstroom Campus, 2004.

Reaction water, a high-strength COD (chemical oxygen demand) petrochemical effluent, is generated during the Fischer-Tropsch reaction in the SASOL Synthol process at SASOL SynFuels, Secunda, South Africa. Distillation of the reaction water to remove non- and oxygenated hydrocarbons yields approximately 25 - 30 ML/d of an organic (carboxylic) acid-enriched stream (average COD of 16 000 mg/L) containing primarily C2 – C5 organic acids, light oils, aldehydes, ketones, cresols and phenols. Together with the Oily sewer water (API) and Stripped Gas Liquor (SGL) process streams, this process effluent is currently treated in ten dedicated activated sludge basins. However, the successful operation of these activated sludge systems has proven to be difficult with low organic loading rates (3.5 kg COD/m3.d) low COD removal efficiencies (<80 %) and high specific air requirements (60 - 75 m3 air/kg CODrem). It is hypothesised that these operational difficulties can be attributed to organic shock loadings, variation in volumetric and hydraulic loadings, as well as variations in the composition of the various process streams being treated. Due to the fact that the Fischer-Tropsch (Synthol) reaction water constitutes 70 % of the COD load on the activated sludge systems, alternative processes to improve the treatment cost and efficiency of the Fischer-Tropsch acid stream are being investigated. Various studies evaluating the aerobic and anaerobic treatment of Fischer-Tropsch reaction water alone in suspended growth wastewater treatment systems have proven unsuccessful. High rate fixed-film processes or biofilm reactors, of which the fluidised-bed reactors are considered to he one of the most effective and promising processes for the treatment of high-strength industrial wastewaters, could he a suitable alternative. The primary aim of this study was to evaluate the suitability of biological fluidised-bed reactors (BFBRs) for the treatment of Fischer-Tropsch reaction water. During this study, the use of aerobic and anaerobic biological fluidised-bed reactors (BFBR), using sand and granular activated carbon (GAC) as support matrices, were evaluated for the treatment of a synthetic effluent analogous to the Fischer-Tropsch reaction water stream. After inoculation, the reactors were operated in batch mode for 10 days at a bed height expansion of 30% and a temperature of 30 ºC to facilitate biofilm formation on the various support matrices. This was followed by continuous operation of the reactors at hydraulic retention times (HRTs) of 2 days. While the COD of the influent and subsequent organic loading rate (OLR) was incrementally increased from 1 600 mg/L to a maximum of 20 000 mg/L and 18 000 mg/L for the aerobic and anaerobic reactors, respectively. Once the maximum influent COD concentration had been achieved the OLR was further increased by decreasing the HRTs of the aerobic and anaerobic reactors to 24h and 8h, and 36h, 24h and 19h, respectively. The dissolved O2 concentration in the main reactor columns of the aerobic reactors was constantly maintained at 0.50 mg/L. Chemical Oxygen Demand (COD) removal efficiencies in excess of 80 % at OLR of up to 30 kg COD/m3.d were achieved in the aerobic BFBRs using both sand and GAC as support matrices. Specific air requirements were calculated to be approximately 35 and 41 m3 air/kg CODrem for the BFBRs using sand and GAC as support matrices, respectively. The oxygen transfer efficiency was calculated to be approximately 5.4 %. At high OLR (> 15 kg COD/m3.d) significant problems were experienced with plugging and subsequent channelling in the BFBR using GAC as support matrix and the reactor had to be backwashed frequently in order to remove excess biomass. Despite these backwash procedures, COD removal efficiencies recovered to previous levels within 24 hours. In contrast, no significant problems were encountered with plug formation and channelling in the BFBR using sand as support matrix. In general the overall reactor performance and COD removal efficiency of the aerobic BFBR using sand as support matrix was more stable and consistent than the BFBR using GAC as support matrix. This BFBR was also more resilient to variations in operational conditions, such as the lowering of the hydraulic retention times and changes in the influent pH. Both aerobic reactors displayed high resilience and COD removal efficiencies in excess of 80 % were achieved during shock loadings. However, both reactors were highly sensitive to changes in pH and any decrease in pH below the pKa values of the volatile fatty acids in the influent (pKa of acetic acid = 4.76) resulted in significant reductions in COD removal efficiencies. Maintenance of reactor pH above 5.0 was thus an essential facet of reactor operation. It has been reported that the VFA/alkalinity ratio can be used to assess the stability of biological reactors. The VFA/alkalinity ratios of the aerobic BFBRs containing sand and GAC as support matrices were stable (VFNalkalinity ratios of < 0.3 - 0.4) until the OLR increased above 10 kg/m3.d. At OLRs higher than 10 kg/m3.d the VFA/alkalinity ratios in the BFBR using sand support matrix increased to 4, above the failure limit value of 0.3 - 0.4. In contrast the VFA/alkalinity ratios of the BFBR using GAC support matrix remained stable until an OLR of 15 kg/m3.d was obtained, where the VFA/alkalinity ratios then increased to > 3. Towards the end of the study when an OLR of approximately 25 kg/m3.d was obtained the VFA/alkalinity ratios of both the BFBRs using sand and GAC as support matrices increased to 9 and 6 respectively, indicating the decrease in reactor stability and acidification of the process. Total solid (TS) and volatile solid (VS) concentrations in the aerobic BFBRs were initially high and decreased over time. While the total suspended solids (TSS) and volatile suspended solids (VSS) concentrations were initially low and increased over time as the OLR was increased, this is thought to be as a result of decreased HRT leading to biomass washout. The anaerobic BFBR using sand as support matrix never stabilised and COD removal efficiency remained very low (< 30 %), possibly due to the high levels of shear forces. Further studies concerning the use of sand as support matrix were subsequently terminated. An average COD removal efficiency of approximately 60 % was achieved in the anaerobic BFBR using GAC as a support matrix at organic loading rates lower than 10 kg COD/m3.d. The removal efficiency gradually decreased to 50 % as organic loading rates were increased to 20 kg COD/m3.d. At OLRs of 20 kg COD/m3.d, the biogas and methane yields of the anaerobic BFBR using GAC as support matrix were determined to be approximately 0.38 m3 biogas/kg CODrem (0.3 m3 biogas/m3reactor vol.d), and 0.20 m3 CH4/kg CODrem (0.23 m3 CH4/m3reactor vol.d), respectively. This value is 57 % of the theoretical maximum methane yield attainable (3.5 m3 CH4/kg CODrem). The methane yield increased as the OLR increased, however, when the OLR reached 8 kg/m3.d the methane yield levelled off and remained constant at approximately 2 m3 CH4/m3reactor vol.d. Although the methane content of the biogas was initially very low (< 30 %), the methane content gradually increased to 60 % at OLRs of 20 kg COD/m3.d. The anaerobic BFBR using GAC as support matrix determined that as the OLR increased (>12 kg/m3.d), the VFA/alkalinity ratio increased to approximately 5, this is indicative of the decrease in stability and acidification of the process. The anaerobic BFBR using GAC as support matrix experienced no problems with plug formation and channelling. This is due to the lower biomass production by anaerobic microorganisms than in the aerobic reactors. The TS and VS concentrations were lower than the aerobic concentrations but followed the same trend of decreasing over time, while the TSS and VSS concentrations increased due to decreased HRTs. The anaerobic BFBR was sensitive to dramatic variations in organic loading rates, pH and COD removal efficiencies decreased significantly after any shock loadings. Compared to the activated sludge systems currently being used for the biological treatment of Fischer-Tropsch reaction water at SASOL SynFuels, Secunda, South Africa, a seven-fold increase in OLR and a 55 % reduction in the specific air requirement was achieved using the aerobic BFBRs. The methane produced could also be used as an alternative source of energy. It is, however, evident that the support matrix has a significant influence on reactor performance. Excellent results were achieved using sand and GAC as support matrices in the aerobic and anaerobic BFBRs, respectively. It is thus recommended that future research be conducted on the optimisation of the use of aerobic and anaerobic BFBRs using these support matrices. Based on the results obtained from this study, it can be concluded that both aerobic and anaerobic treatment of a synthetic effluent analogous to the Fischer-Tropsch reaction water as generated by SASOL in the Fischer-Tropsch Synthol process were successful and that the application of fluidised-bed reactors (attached growth systems) could serve as a feasible alternative technology when compared to the current activated sludge treatment systems (suspended growth) currently used. Keywords: aerobic treatment, anaerobic treatment, biological fluidised-bed reactors, petrochemical effluent, Fischer-Tropsch reaction water, industrial wastewater. / Thesis (M. Omgewingswetenskappe)--North-West University, Potchefstroom Campus, 2004.

L'alumine, utilisée comme support de catalyseurs pour la réaction de Fischer-Tropsch ou pour la conversion de la biomasse, se transforme partiellement en présence d'eau en phases (oxy)hydroxydes à l'origine de fines qui posent problème dans la mise en ¿uvre de procédés en réacteurs de type slurry. Afin de concevoir des catalyseurs plus stables et plus résistants, ce travail de thèse visait à identifier le mécanisme d'hydratation et de dégradation des alumines de transition en phase aqueuse, et à étudier la façon dont des additifs organiques (alcools, polyols) ou inorganiques (Mg, Zr, Ni et Si) permettent de limiter cette dégradation. La conduite d'une étude systématique sur l'hydratation des alumines à 70°C à pression atmosphérique, ou à 150°C en conditions hydrothermales, a permis de définir un mécanisme général en deux étapes: une dissolution de la surface de l'alumine, suivie d'une précipitation, respectivement, d'hydroxydes d'aluminium Al(OH)3 ou de boehmite AlOOH sur les grains d'alumine. Par ailleurs, la dégradation chimique tend à favoriser la dégradation sous contraintes mécaniques. La présence de polyols en phase aqueuse, principalement des molécules à 5 ou 6 atomes de carbone, ralentit la dissolution de l'alumine et inhibe la précipitation de la boehmite. Les ions métalliques utilisés comme dopants de l'alumine ont tous un effet similaire sur la diminution de l'hydratation. Une inhibition totale de l'hydratation est obtenue par greffage de silicium à partir de TEOS. Une étude DRIFT dans la région des vibrations OH suggère que les additifs inorganiques inhibent la dissolution de l'alumine en bloquant des sites Al-OH localisés sur les faces latérales des particules. / Alumina, used as a catalyst support for the Fischer-Tropsch reaction or for the conversion of biomass, partially transforms in presence of water into (oxy)hydroxides phases. The formation of the latter leads to the production of fine particles that may cause plugging problems in the implementation of processes based on slurry bubble column reactors. In order to design more stable and more resistant catalysts, this PhD work aimed at identifying the mechanism of hydration and degradation of transition aluminas in aqueous phase, and to study how organic (alcohols, polyols) or inorganic (Mg, Zr, Ni and Si) additives can limit this degradation. The conduct of a systematic study on the hydration of alumina at 70°C under atmospheric pressure, or at 150°C in hydrothermal conditions, allowed defining a general two-step mechanism: a dissolution of the surface of alumina, followed by a precipitation of, respectively, aluminum hydroxides (Al(OH)3) or boehmite (AlOOH) on alumina grains. Furthermore, the chemical degradation tends to promote the degradation under mechanical stress. The presence of polyols in aqueous phase, mainly molecules with 5 or 6 carbon atoms, slows down the dissolution of alumina and inhibit the precipitation of boehmite. Metal ions used as dopants of alumina all have a similar effect on the decrease of hydration. A total inhibition of hydration is obtained by grafting silicon using TEOS. A DRIFTS study in the OH vibration region suggests that inorganic additives inhibit the dissolution of alumina by blocking Al-OH sites located on the lateral facets of the particles.

nÃo hà / O presente trabalho tem como principal objetivo investigar as condiÃÃes mais adequadas para o estudo da difusividade de n-parafinas em um catalisador tÃpico para a sÃntese de Fischer-Tropsch (SFT), utilizando o mÃtodo cromatogrÃfico ZLC (coluna de comprimento zero), e avaliando-se a repetitividade e a reprodutibilidade desta metodologia. Objetiva, ainda, verificar o desempenho do catalisador em um reator de leito fixo, em escala piloto, e observar o efeito da difusÃo na seletividade a hidrocarbonetos de alta massa molar. O catalisador foi caracterizado, com Ãnfase nos ensaios de microscopia e anÃlise textural. Quanto à difusividade dos n-alcanos (n-C7, n-C9, n-C12, n-C16), foram utilizados dois sistemas ZLC, sendo um na Universidade Federal do Cearà (UFC) e o outro na Universidade de Edimburgo, empregando-se amostras de diferentes granulometrias (forma pà e pellet). Investigou-se, tambÃm, a influÃncia da temperatura, da vazÃo do gÃs de purga, da massa de catalisador e da concentraÃÃo do sorbato no gÃs de purga. Quanto à etapa reacional, esta ocorreu em uma unidade piloto para a SFT a 20 bar, nas temperaturas de 210 ÂC e 230 ÂC e em diferentes velocidades espaciais. O catalisador apresentou-se como mesoporoso, com um pouco de microporosidade, e com a fase ativa (Co) bem distribuÃda. Em relaÃÃo à difusividade efetiva, o diÃmetro de partÃcula mais adequado para o uso na coluna ZLC, dentre os testados, foi de 214 Âm para o catalisador na forma pÃ, com 5 mg de amostra. Comparando-se os experimentos realizados nas duas universidades, percebeu-se uma boa repetitividade, porÃm a reprodutibilidade, nÃo foi satisfatÃria. Observou-se ainda, a influÃncia da constante de Henry nos resultados obtidos para difusividade efetiva, em diferentes tamanhos de catalisador, entretanto, nÃo se perceberam mudanÃas significativas na difusividade efetiva em funÃÃo da variaÃÃo da temperatura e da concentraÃÃo de sorbato no gÃs de purga. Em se tratando da reaÃÃo, os resultados indicaram um forte efeito da temperatura na conversÃo de CO e na seletividade a C5+. O mecanismo difusivo à afetado pela difusividade de superfÃcie, e, a partir deste resultado, pode-se justificar o aumento da seletividade a metano com o incremento da relaÃÃo H2/CO. Com base nos resultados apresentados, o mÃtodo ZLC mostrou-se adequado para o estudo da difusividade efetiva de n-parafinas em um catalisador convencional para a SFT. / The main goal of the present research is to establish the most appropriate conditions for studying the diffusivity of n-paraffins in the presence of a typical catalyst for Fischer-Tropsch synthesis (FTS), by using the chromatographic method ZLC (zero length column) and evaluating the repeatability and reproducibility of this method. It also aims to verify the catalyst performance in a fixed bed reactor, at a pilot-scale, and observe the effect of diffusion in the selectivity of high molar mass hydrocarbons. At first, the catalyst characterization was done with emphasis on the microscopy studies and textural analysis with N2. Regarding the n-alkanes diffusivity (n-C7, n-C9, n-C12, n-C16), two ZLC equipments were used, one at the Federal University of Ceara (UFC) and the another one at the University of Edinburgh, with different particle size samples. This work has also evaluated the influence of temperature, the purge gas flow rate, the catalyst mass and sorbate concentration in the purge gas. The reaction step was done at a Fisher-Tropsch pilot-scale unit at 20 bar, with 210ÂC and 230ÂC in different space velocities. As a result, the catalyst was presented as mesoporous, with small microporosity, and with active phase (Co) well distributed. Concerning the effective diffusivity, the most appropriate particle diameter to be used at the ZLC column, among the tested diameters, is 214 Âm (dust form), with 5 mg of catalyst. Comparing the studies that were held at the two universities, it was noticed a good repeatability, however, the reproducibility was not satisfactory. It was observed a strong influence of the HenryÂs constant at the results of effective diffusivity, for different catalyst sizes; however, no significant changes at the effective diffusivity were noted due to temperature variation and sorbate concentration. Regarding the reaction, the results indicated a strong effect of temperature at the CO conversion and at the C5+ selectivity. The diffusive mechanism is strongly affected by the catalyst surface effects. Based on this result, the raise of methane selectivity by increasing H2/CO ratio can explained. As final result, the ZLC is found as a suitable method for surface diffusion estimation using typical Fischer-Tropsch catalyst.

During this PhD thesis, cobalt (Co) catalysts have been prepared, characterized and studied in the carbon monoxide hydrogenation (CO+H2) reaction (also known as “Fischer-Tropsch” (FT) reaction). In industry, the FT synthesis aims at producing long chain hydrocarbons such as gasoline or diesel fuels. The interest is that the reactants (CO and H2) are obtained from other carbonaceous sources than crude oil: natural gas, coal, biomass or even petroleum residues. As it is well known that the worldwide crude oil reserves will be depleted in a few decades, the FT reaction represents an attractive alternative for the production of various fuels. Moreover, this reaction can also be used to produce high value specialty chemicals (long chain alcohols, light olefins…).<p>Two different types of catalysts have been investigated during this thesis: cobalt with magnesia used as support or dispersant (Co/MgO) and cobalt with silica used as support (Co/SiO2). Each catalyst from the first class is prepared by precipitation of a mixed Co/Mg oxalate in acetone. This coprecipitation is followed by a thermal decomposition under reductive atmosphere leading to a mixed Co/MgO catalyst. On the other hand, Co/SiO2 catalysts are prepared by impregnation of a commercial silica support with a chloroform solution containing Co nanoparticles. This impregnation is then followed by a thermal activation under reductive atmosphere.<p>The mixed Co/Mg oxalates and the resulting Co/MgO catalysts have been extensively characterized in order to gain a better understanding of the composition, the structure and the morphology of these materials: thermal treatments under reductive and inert atmospheres (followed by MS, DRIFTS, TGA and DTA), BET surface area measurements, XRD and electron microscopy studies have been performed. Moreover, an original in situ technique for measuring the H2 chemisorption surface area of catalysts has been developed and used over our catalysts.<p>The performances of the Co/MgO and Co/SiO2 catalysts have then been evaluated in the CO+H2 reaction at atmospheric pressure. Chemical Transient Kinetics (CTK) experiments have been carried out in order to obtain information about the reaction kinetics and mechanism and the nature of the catalyst active surface under reaction conditions. The influence of several experimental parameters (temperature, H2 and CO partial pressures, total volumetric flow rate) and the effect of passivation are also discussed with regard to the catalyst behavior.<p>Our results indicate that the FT active surface of Co/MgO 10/1 (molar ratio) is entirely covered by carbon, oxygen and hydrogen atoms, most probably associated as surface complexes (possibly formate species). Thus, this active surface does not present the properties of a metallic Co surface (this has been proved by performing original experiments consisting in switching from the CO+H2 reaction to the propane hydrogenolysis reaction (C3H8+H2) which is sensitive to the metallic nature of the catalyst). CTK experiments have also shown that gaseous CO is the monomer responsible for chain lengthening in the FT reaction (and not any CHx surface intermediates as commonly believed). Moreover, CO chemisorption has been found to be irreversible under reaction conditions.<p>The CTK results obtained over Co/SiO2 are quite different and do not permit to draw sharp conclusions concerning the FT reaction mechanism. More detailed studies would have to be carried out over these samples.<p>Finally, Co/MgO catalysts have also been studied on a combined DRIFTS/MS experimental set-up in Belfast. CTK and Steady-State Isotopic Transient Kinetic Analysis (SSITKA) experiments have been carried out. While formate and methylene (CH2) groups have been detected by DRIFTS during the FT reaction, the results indicate that these species play no role as active intermediates. These formates are most probably located on MgO or at the Co/MgO interface, while methylene groups stand for skeleton CH2 in either hydrocarbon or carboxylate. Unfortunately, formate/methylene species have not been detected by DRIFTS over pure Co catalyst without MgO, because of the full signal absorption.<p> / Doctorat en Sciences de l'ingénieur / info:eu-repo/semantics/nonPublished

[ES] La presente tesis doctoral se centra en el desarrollo de nuevas membranas de separación de gases, así como su empleo in-situ en reactores catalíticos de membrana para la intensificación de procesos. Para este propósito, se han sintetizado varios materiales, como polímeros para la fabricación de membranas, catalizadores tanto para la metanación del CO2 como para la reacción de síntesis de Fischer-Tropsch, y diversas partículas inorgánicas nanométricas para su uso en membranas de matriz mixta. En lo referente a la fabricación de las membranas, la tesis aborda principalmente dos tipos: orgánicas e inorgánicas. Con respecto a las membranas orgánicas, se han considerado diferentes materiales poliméricos, tanto para la capa selectiva de la membrana, así como soporte de la misma. Se ha trabajado con poliimidas, puesto que son materiales con temperaturas de transición vítrea muy alta, para su posterior uso en reacciones industriales que tienen lugar entre 250-300 ºC. Para conseguir membranas muy permeables, manteniendo una buena selectividad, es necesario obtener capas selectivas de menos de una micra. Usando como material de soporte otro tipo de polímero, no es necesario estudiar la compatibilidad entre ellos, siendo menos compleja la obtención de capas finas. En cambio, si el soporte es de tipo inorgánico, un exhaustivo estudio de la relación entre la concentración y la viscosidad de la solución polimérica es altamente necesario. Diversas partículas inorgánicas nanométricas se estudiaron para favorecer la permeación de agua a través de los materiales poliméricos. En segundo lugar, en cuanto a membranas inorgánicas, se realizó la funcionalización de una membrana de paladio para favorecer la permeación de hidrógeno y evitar así la contaminación por monóxido de carbono. El motivo por el cual se dopó con otro metal la capa selectiva de la membrana metálica fue para poder emplearla en un reactor de Fischer-Tropsch. Con relación al diseño y fabricación de los reactores, durante esta tesis, se desarrolló el prototipo de un microreactor para la metanación de CO2, donde una membrana polimérica de capa fina selectiva al agua se integró para evitar la desactivación del catalizador, y a su vez desplazar el equilibrio y aumentar la conversión de CO2. Por otro lado, se rediseñó un reactor de Fischer-Tropsch para poder introducir una membrana metálica selectiva a hidrogeno y poder inyectarlo de manera controlada. De esta manera, y siguiendo estudios previos, el objetivo fue mejorar la selectividad a los productos deseados mediante el hidrocraqueo y la hidroisomerización de olefinas y parafinas con la ayuda de la alta presión parcial de hidrógeno. / [CAT] La present tesi doctoral es centra en el desenvolupament de noves membranes de separació de gasos, així com el seu ús in-situ en reactors catalítics de membrana per a la intensificació de processos. Per a aquest propòsit, s'han sintetitzat diversos materials, com a polímers per a la fabricació de membranes, catalitzadors tant per a la metanació del CO2 com per a la reacció de síntesi de Fischer-Tropsch, i diverses partícules inorgàniques nanomètriques per al seu ús en membranes de matriu mixta. Referent a la fabricació de les membranes, la tesi aborda principalment dos tipus: orgàniques i inorgàniques. Respecte a les membranes orgàniques, diferents materials polimèrics s'ha considerat com a candidats prometedors, tant per a la capa selectiva de la membrana, així com com a suport d'aquesta. S'ha treballat amb poliimides, ja que són materials amb temperatures de transició vítria molt alta, per al seu posterior ús en reaccions industrials que tenen lloc entre 250-300 °C. Per a aconseguir membranes molt permeables, mantenint una bona selectivitat, és necessari obtindre capes selectives de menys d'una micra. Emprant com a material de suport altre tipus de polímer, no és necessari estudiar la compatibilitat entre ells, sent menys complexa l'obtenció de capes fines. En canvi, si el suport és de tipus inorgànic, un exhaustiu estudi de la relació entre la concentració i la viscositat de la solució polimèrica és altament necessari. Diverses partícules inorgàniques nanomètriques es van estudiar per a afavorir la permeació d'aigua a través dels materials polimèrics. En segon lloc, quant a membranes inorgàniques, es va realitzar la funcionalització d'una membrana de pal¿ladi per a afavorir la permeació d'hidrogen i evitar la contaminació per monòxid de carboni. El motiu pel qual es va dopar amb un altre metall la capa selectiva de la membrana metàl¿lica va ser per a poder emprar-la en un reactor de Fischer-Tropsch. En relació amb el disseny i fabricació dels reactors, durant aquesta tesi, es va desenvolupar el prototip d'un microreactor per a la metanació de CO2, on una membrana polimèrica de capa fina selectiva a l'aigua es va integrar per a així evitar la desactivació del catalitzador i al seu torn desplaçar l'equilibri i augmentar la conversió de CO2. D'altra banda, un reactor de Fischer-Tropsch va ser redissenyat per a poder introduir una membrana metàl¿lica selectiva a l'hidrogen i poder injectar-lo de manera controlada. D'aquesta manera, i seguint estudis previs, el objectiu va ser millorar la selectivitat als productes desitjats mitjançant el hidrocraqueix i la hidroisomerització d'olefines i parafines amb l'ajuda de l'alta pressió parcial d'hidrogen. / [EN] The present thesis is focused on the development of new gas-separation membranes, as well as their in-situ integration on catalytic membrane reactors for process intensification. For this purpose, several materials have been synthesized such as polymers for membrane manufacture, catalysts for CO2 methanation and Fischer-Tropsch synthesis reaction, and inorganic materials in form of nanometer-sized particles for their use in mixed matrix membranes. Regarding membranes manufacture, this thesis deals mainly with two types: organic and inorganic. With regards to the organic membranes, different polymeric materials have been considered as promising candidates, both for the selective layer of the membrane, as well as a support thereof. Polyimides have been selected since they are materials with very high glass transition temperatures, in order to be used in industrial reactions which take place at temperatures around 250-300 ºC. To obtain highly permeable membranes, while maintaining a good selectivity, it is necessary to develop selective layers of less than one micron. Using another type of polymer as support material, it is not necessary to study the compatibility between membrane and support. On the other hand, if the support is inorganic, an exhaustive study of the relation between the concentration and the viscosity of the polymer solution is highly necessary. In addition, various inorganic particles were studied to favor the permeation of water through polymeric materials. Secondly, as regards to inorganic membranes, the functionalization of a palladium membrane to favor the permeation of hydrogen and avoid carbon monoxide contamination was carried out. The membrane selective layer was doped with another metal in order to be used in a Fischer-Tropsch reactor. Regarding the design and manufacture of the reactors used during this thesis, a prototype of a microreactor for CO2 methanation was carried out, where a thin-film polymer membrane selective to water was integrated to avoid the deactivation of the catalyst and to displace the equilibrium and increase the CO2 conversion. On the other hand, a Fischer-Tropsch reactor was redesigned to introduce a hydrogen-selective metal membrane and to be able to inject it in a controlled manner. In this way, and following previous studies, the aim is to enhance the selectivity to the target products by hydrocracking and hydroisomerization the olefins and paraffins assisted by the presence of an elevated partial pressure of hydrogen. / I would like to acknowledge the Spanish Government, for funding my research with the Severo Ochoa scholarship. / Escorihuela Roca, S. (2019). Novel gas-separation membranes for intensified catalytic reactors [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/121139 / TESIS