Abstract:
An alkylation process utilizing less than 10 vol % of a halometallate based ionic liquid catalyst is described. By decreasing the catalyst volume fraction, the level of subsequent undesirable reactions may be minimized. The total residence time is typically in the range of about 1 min to about 30 min. The alkylate typically has a research octane number of at least about 93, and the olefin conversion is typically at least about 96%.
Abstract:
A process utilizing an ionic liquid is described. The process includes contacting a hydrocarbon feed with an ionic liquid component, the ionic liquid component comprising a mixture of a first ionic liquid and a viscosity modifier, wherein a viscosity of the ionic liquid component is at least about 10% less than a viscosity of the first ionic liquid.
Abstract:
Processes have been developed for oxidizing alkyl aromatic compounds, and which reduce the amount of 4-CBA in the solid oxidation products. The process can reduce the makeup amount of ionic liquid, carboxylic acid, catalyst, bromine source, and ammonia source.
Abstract:
A process for oxidizing alkyl aromatic compounds is described. The alkyl aromatic compound is oxidized producing an aromatic carboxylic acid, and an aromatic amide compound. The aromatic amide compound is then hydrolyzed with a hydrolyzing agent to the aromatic carboxylic acid.
Abstract:
Processes have been developed to obtain recycle ionic liquid streams which are active for oxidation of alkyl aromatic compounds, and which reduce the amount of 4-CBA in the solid oxidation products. The process can reduce the makeup amount of ionic liquid, carboxylic acid, catalyst, bromine source, and ammonia source.
Abstract:
A renewable feed that is concentrated linear C10-C13 paraffins is produced by hydrodeoxygenating a renewable feedstock is produced by first hydrotreating the feedstock to remove heteroatoms followed by use of a Group VI or VIII catalyst producing a 10-13 carbon atom product having a high level of linearity. Normal paraffins in the range desired by the detergents industry can be produced.
Abstract:
A fluidized reforming process comprising a two stage fluidized reforming reactor is described. A naphtha stream flows upward through the two fluidized stages and contacts the catalyst forming a product stream and spent catalyst. The spent catalyst is separated from the product stream and the naphtha feed stream. Some of the spent catalyst is regenerated by contact with an oxygen-containing regeneration fluid to heat and reactivate the catalyst. The heated, regenerated catalyst forms at least a port of the catalyst stream for the process. A process for cyclizing paraffins or isomerizing cyclopentanes is also described. The process uses a chloride-free Pt/Ga-containing catalyst to form a cyclic aliphatic hydrocarbon or isomerizing a cyclopentane in the presence of the chloride-free Pt/Ga-containing catalyst to form a cyclohexane.
Abstract:
A de-hydrogenation catalyst and its use in dehydrogenation of hydrocarbons. The catalyst has low cracking activity and comprises gallium or gallium and platinum on an essentially non-acidic and amorphous alumina-phosphate or silica-alumina-phosphate support with an empirical chemical composition of [Al2O3][SiO2]Y[P2O5]Z, wherein Y is between 0 and 0.2 and Z is between 0.01 and 1.1, with a BET surface area above 50 m2/g, as measured by N2 adsorption experiment.
Abstract:
A trialkylphosphonium haloaluminate compound having a formula: where R1, R2, and R3 are the same or different and each is independently selected from C1 to C8 hydrocarbyl; and X is selected from F, Cl, Br, I, or combinations thereof is described. An ionic liquid catalyst composition incorporating the trialkylphosphonium haloaluminate compound, methods of making the trialkylphosphonium haloaluminate compound, and alkylation processes incorporating the trialkylphosphonium haloaluminate compound are also described.
Abstract:
Non-cyclic amide or thioamide based ionic liquids and methods of making them are disclosed. The non-cyclic amide or thioamide based ionic liquid comprises a cation and an anion and has the formula: