The present invention provides a process to prepare a composite ionic liquid, the process at least comprising the steps: (a) mixing an ammonium salt and a solid aluminium salt to obtain a first mixture; (b) stirring under heating the first mixture of step (a); (c) adding to the first mixture of step (b) one or more solid metal salts to obtain a second mixture, wherein the metal salts are selected from halides, sulfates, or nitrates of aluminium, gallium, copper, iron, zinc, nickel, cobalt, molybdenum and platinum; (d) stirring under heating the second mixture of step (c); (e) adding to the second mixture of step (d) a hydrocarbon to obtain a third mixture; (f) stirring under heating the third mixture of step (e) until the solids of the aluminium salt of step (a), and the solids of the metal salts of step (c) disappear and the mixture is converted into a composite ionic liquid; and (g) cooling the composite ionic liquid of step (f).

The present invention provides a process to prepare a composite ionic liquid, the process at least comprising the steps: (a) mixing an ammonium salt and a solid aluminium salt to obtain a first mixture; (b) stirring under heating the first mixture of step (a); (c) adding to the first mixture of step (b) one or more solid metal salts to obtain a second mixture, wherein the metal salts are selected from halides, sulfates, or nitrates of aluminium, gallium, copper, iron, zinc, nickel, cobalt, molybdenum and platinum; (d) stirring under heating the second mixture of step (c); (e) adding to the second mixture of step (d) a hydrocarbon to obtain a third mixture; (f) stirring under heating the third mixture of step (e) until the solids of the aluminium salt of step (a), and the solids of the metal salts of step (c) disappear and the mixture is converted into a composite ionic liquid; and (g) cooling the composite ionic liquid of step (f).

The present invention provides a process to prepare a composite ionic liquid, the process at least comprising the steps: (a) mixing an ammonium salt and a solid aluminium salt to obtain a first mixture; (b) stirring under heating the first mixture of step (a); (c) adding to the first mixture of step (b) one or more solid metal salts to obtain a second mixture, wherein the metal salts are selected from halides, sulfates, or nitrates of aluminium, gallium, copper, iron, zinc, nickel, cobalt, molybdenum and platinum; (d) stirring under heating the second mixture of step (c); (e) adding to the second mixture of step (d) a hydrocarbon to obtain a third mixture; (f) stirring under heating the third mixture of step (e) until the solids of the aluminium salt of step (a), and the solids of the metal salts of step (c) disappear and the mixture is converted into a composite ionic liquid; and (g) cooling the composite ionic liquid of step (f).

Processes for the direct alkylation of ethylene with isobutane or isopentane using a highly active ionic liquid alkylation catalyst are described. Ethylene is sent to a high-temperature alkylation reactor loop, and C.sub.3, C.sub.4, and C.sub.5 olefins are routed to a low temperature alkylation reactor loop. In each reactor, the olefins are contacted with an excess of isobutane or isopentane in the presence of a highly active ionic liquid catalyst. Portions of the reactor effluent streams are fed to a common downstream catalyst separation and product fractionation sections. The remainder of the reactor effluent is recycled back to the respective alkylation reactor.

Processes for the direct alkylation of ethylene with isobutane or isopentane using a highly active ionic liquid alkylation catalyst are described. Ethylene is sent to a high-temperature alkylation reactor loop, and C.sub.3, C.sub.4, and C.sub.5 olefins are routed to a low temperature alkylation reactor loop. In each reactor, the olefins are contacted with an excess of isobutane or isopentane in the presence of a highly active ionic liquid catalyst. Portions of the reactor effluent streams are fed to a common downstream catalyst separation and product fractionation sections. The remainder of the reactor effluent is recycled back to the respective alkylation reactor.

A trialkylphosphonium haloaluminate compound having a formula: ##STR00001##
where R.sup.1, R.sup.2, and R.sup.3 are the same or different and each is independently selected from C.sub.1 to C.sub.8 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.

A trialkylphosphonium haloaluminate compound having a formula: ##STR00001##
where R.sup.1, R.sup.2, and R.sup.3 are the same or different and each is independently selected from C.sub.1 to C.sub.8 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.

The present invention provides a process for preparing (7Z)-7-tricosene of the following formula (3): the process comprising a step of subjecting a nucleophilic reagent, (8Z)-8-pentadecenyl compound of the following general formula (1), wherein M.sup.1 represents Li, MgZ.sup.1, CuZ.sup.1 or CuLiZ.sup.1, wherein Z.sup.1 represents a halogen atom or an (8Z)-8-pentadecenyl group, to a coupling reaction with a 1-halooctane compound of the following general formula (2), wherein X.sup.1 represents a halogen atom, to produce (7Z)-7-tricosene (3). ##STR00001##

The present invention provides a process for preparing (7Z)-7-tricosene of the following formula (3): the process comprising a step of subjecting a nucleophilic reagent, (8Z)-8-pentadecenyl compound of the following general formula (1), wherein M.sup.1 represents Li, MgZ.sup.1, CuZ.sup.1 or CuLiZ.sup.1, wherein Z.sup.1 represents a halogen atom or an (8Z)-8-pentadecenyl group, to a coupling reaction with a 1-halooctane compound of the following general formula (2), wherein X.sup.1 represents a halogen atom, to produce (7Z)-7-tricosene (3). ##STR00001##

An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.