This thesis presents the results of an experiment conducted to discover if selenic acid or monazite sand are possible catalysts that can be used for the alkylation of isobutane and isobutene.

This study investigated mercury-sensitized photochemical action on a mixture of isobutane and isobutene. Flow runs of isobutane-isobutene 3.2.1 mercury-saturated gases illuminated with unfiltered radiation of mercury vapor lamp gave no detectable change to hydrocarbons heavier than C4 at reaction tempratures of 27C. and 99C.

A study of the effect of photo-sensitized mercury on mixtures of isobutane and isobutene.

This thesis describes a fractionation column method of separating isobutane and isobutene to isolate isooctane.

The world is currently faced with the enormous challenge of slowing down human triggered global warming. As the global energy demand increases, there is an urgent need for renewable and carbon-neutral fuel-sources. Isoprene and isobutene are crude-oil derived, short, volatile and reactive hydrocarbons that can be polymerised into longer chains to be used as jet fuel. Isoprene has previously been produced from the cyanobacterial strain Synechocystis sp. PCC 6803 but there has been no reported isobutene synthesis from any photosynthetic organism. This work aimed to synthesise isobutene in Synechocystis using a cytochrome P450 from Cystobasidium minutum with reported isobutene production capability. Substrate availability was to be provided through the insertion of two heterologous enzymes, IpdC from Salmonella typhimurium and PadA from Escherichia coli. Both IpdC and PadA were successfully expressed in Synechocystis but the functional activities of IpdC, PadA and the cytochrome P450 in Synechocystis remains undetermined. This project also had the aim to design and construct a photo-bioreactor and gas collection system capable of producing and harvesting isoprene directly from an engineered Synechocystis strain. Herein lies a description of a closed system photobioreactor connected to a cold-trap that was able to concentrate isoprene produced from Synechocystis to measurable amounts.

L´objectif du travail présenté dans ce manuscrit consiste à conserver les bonnes propriétés mécaniques du poly(butadiène) dihydroxytéléchélique (PBHT) tout en améliorant sa stabilité. Un des principaux verrous techniques de cette approche réside dans le fait que les doubles liaisons responsables la flexibilité du matériau sont également la cause de son vieillissement par oxydation. Les solutions proposées reposent sur l´utilisation de la métathèse comme outils de synthèse de polymères insaturés. Deux grandes voix de synthèse ont été étudiées : la polymérisation par ouverture de cycle via métathèse (ROMP) ainsi que la dépolymerisation fonctionnalisante (ADMET). Ces deux approches bien que prometteuses n’ont pas permis de sortir de la relation ciseau existante entre flexibilité et stabilité. Finalement, une solution basée sur le mélange entre deux polymères dihydroxytéléchéliques de basse température de transition vitreuse – poly(butadiene) et poly(isobutylene) a permis de répondre dans une certaine mesure aux cahier des charges. En parallèle a ces parties synthèses, une étude physique des relations structure-propriétés visant à améliorer la stabilité des oligomères a été apporté par mesure rhéologique du temps critique de réticulation. / The work reported in the following document is aiming at maintaining the good mechanical properties of diHydroxyTelechelic PolyButadiene HTPB while improving its stability. The major challenge of this approach is that the unsaturations responsible for the outstanding flexibility of the material are also rather sensitive to oxidation. The solutions presented in this study are based on the use of metathesis reactions as a tool for the design of new difunctional unsaturated oligomers. Two functionalization techniques have been investigated, on the one hand, the Ring Opening Methathesis Polymerisation (ROMP) and, on the other hand, the depolymerisation via Acyclic Diene METathesis (ADMET). Although promising, the latters proved to fall into the vicious circle consisting in simultaneously increasing the stability while losing the flexibility. Finally, a blending concept based on the mixture of two dihydroxytelechelic polymers, namely, poly(isobutylene) and poly(butadiene), could enable us to achieve our initial goal. In addition to the chapters focusing on polymer chemistry and synthesis, a physical study of the parameters influencing the aging of unsaturated oligomers have been set-up and the properties relationship using measurements of the critical time.

[pt] Nos últimos anos, a crescente preocupação com o meio ambiente tem impulsionado o desenvolvimento de processos alternativos e sustentáveis para a obtenção de compostos importantes na indústria química. O isobuteno é um hidrocarboneto, comumente utilizado como intermediário para a síntese de diversos produtos, como polímeros e aditivos de combustíveis. A principal forma de produção desse hidrocarboneto é a partir do craqueamento da nafta, pelo qual é produzido como um coproduto por uma via dependente de fontes fósseis. Para atender à demanda de isobuteno associado a uma produção sustentável, novos estudos têm sugerido a síntese dessa olefina a partir da conversão catalítica de compostos como o etanol, uma matériaprima renovável que pode ser obtida a partir do processamento de diferentes biomassas. Experimentos recentes mostraram que uma mistura física In2O3+ZrO2 apresenta o mesmo desempenho de catalisadores In2O3/ZrO2, sendo ambos promissores para esse tipo de reação química. Assim, o objetivo deste estudo consiste em investigar esta mistura física como catalisador na síntese do isobuteno a partir do etanol. Nesta pesquisa, os catalisadores In2O3, ZrO2 e uma mistura física In2O3+ZrO2 foram avaliados por testes catalíticos em leito fixo e caracterizados pelas técnicas de DRX, XPS, EPR, TPD (CO, CO2, isopropanol, etanol e acetona), Fisissorção de N2, TPR-H2 e espectroscopia de infravermelho com adsorção de piridina. Os resultados revelam que a mistura física apresenta uma atividade catalítica superior ao In2O3 e ao ZrO2 puros, sendo capaz de formar isobuteno com uma seletividade de 36 por cento. O efeito sinérgico desses dois óxidos é verificado, resultando na formação de vacâncias catiônicas e aniônicas no catalisador MF, bem como promovendo as propriedades redox e básicas do sistema. / [en] In recent years, the growing concern with the environment has driven the development of alternative and sustainable processes to obtain important compounds in the chemical industry. Isobutene is a hydrocarbon commonly used as an intermediate for the synthesis of various products such as polymers and fuel additives. The main form of the production of this hydrocarbon is from the cracking of naphtha, by which it is produced as a co-product by a pathway dependent on fossil sources. To meet the demand for isobutene associated with sustainable production, new studies have suggested the synthesis of this olefin from the catalytic conversion of compounds such as ethanol, a renewable raw material that can be obtained from the processing of different biomasses. Recent experiments have shown that an In2O3+ ZrO2 physical mixture (MF) has the same performance as In2O3/ZrO2 catalysts, both of which are promising for this type of chemical reaction. Thus, the aim of this study is to investigate this physical mixture as a catalyst in the synthesis of isobutene from ethanol. In this research, the In2O3, ZrO2 catalysts and an In2O3+ZrO2 physical mixture were evaluated by fixed bed catalytic tests and characterized by the techniques of XRD, XPS, EPR, TPD (CO, CO2, isopropanol, ethanol and acetone), N2 physisorption, TPR-H2 and infrared spectroscopy with pyridine adsorption. The results show that the physical mixture has a catalytic activity superior to pure oxides, In2O3 and ZrO2, being able to form isobutene with a selectivity of 36 percent. The synergistic effect of these two oxides is verified, resulting in the formation of cationic and anionic vacancies in the MF catalyst, as well as promoting the redox and basic properties of the system.