Abstract: The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid stream comprising aliphatic hydrocarbons, heteroatom containing organic compounds and optionally aromatic hydrocarbons, involving a) contacting said liquid stream with a stream having a pH above 7 and comprising a washing solvent, preceded and/or followed by contacting with a stream having a pH below 7 and comprising a washing solvent; b) liquid-liquid extraction of the washed stream with an extraction solvent. Further, the invention relates to a process for the recovery of aliphatic hydrocarbons from plastics comprising the above-mentioned process; and to a process for steam cracking a hydrocarbon feed comprising aliphatic hydrocarbons as recovered in one of the above-mentioned processes.

Abstract: The invention relates to a process for converting plastics waste into pyrolysis oil for feeding to a steam cracker including the steps of: pre-washing a stream of comminuted waste plastics in a washing liquid comprising washing water and caustic solution; separating the pre-washed comminuted waste plastics to provide a stream of polyolefin-enriched washed comminuted plastics waste; thermally cracking the stream of polyolefin-enriched washed comminuted plastics waste to produce a vaporised hydrocarbon stream; condensing the vaporised hydrocarbon stream into a liquid hydrocarbon stream and gaseous hydrocarbon stream; washing the liquid hydrocarbon stream with caustic solution; separating the liquid hydrocarbon stream from the caustic solution to produce a stream of caustic-washed liquid hydrocarbon and a stream of spent caustic solution; and rinsing the caustic-washed liquid hydrocarbon stream with water; separating the rinsed liquid hydrocarbon stream from the rinsing water to produce a stream of pyrolysis oil

Abstract: A process for converting carbon dioxide and hydrogen into a product stream comprising carbon monoxide, water and hydrogen by introducing carbon dioxide, hydrogen and oxygen into a reaction vessel, and performing a reverse water gas shift reaction at elevated temperature, wherein (a) no catalyst is present in vessel (b) gas stream comprising carbon dioxide, a hydrogen and an oxygen rich gas stream are introduced into the vessel in separate feed streams, (c) the hydrogen and oxygen rich gas stream being introduced in close vicinity of each other, via burner comprising coaxial channels wherein gases undergo a combustion reaction, providing the heating energy required for the reverse water-gas shift reaction; and (d) the temperature in vessel is in the range of 1000 to 1500° C. by varying the molar ratio of hydrogen to oxygen. It is useful in reducing the carbon footprint of certain industrial technologies, and in production of synthesis gas.

Abstract: The invention relates to a process for the recovery of aliphatic hydrocarbons from a liquid stream comprising aliphatic hydrocarbons, heteroatom containing organic compounds and optionally aromatic hydrocarbons, involving a) contacting said liquid stream with a washing solvent thereby removing heteroatom containing organic compounds; b) liquid-liquid extraction of the washed stream with an extraction solvent; wherein heteroatom containing organic compounds, optional aromatic hydrocarbons and optional other contaminants are removed from said liquid stream and/or from a washed stream resulting from step a) and/or from a raffinate stream resulting from step b), respectively, by contacting the latter stream(s) with a sorption agent. Further, the invention relates to a process for the recovery of aliphatic hydrocarbons from plastics comprising the above-mentioned process; and to a process for steam cracking a hydrocarbon feed comprising aliphatic hydrocarbons as recovered in one of the above-mentioned processes.

Abstract: The present invention relates to a process for converting feed streams selected from (1) a gas stream comprising carbon dioxide and a hydrogen rich gas stream; (2) a methane rich gas stream; and (3) a combination of feed streams (1) and (2) into a product stream comprising carbon monoxide, water and hydrogen. The process may include introducing feed streams selected from (1), (2) or (3) and oxygen into a reaction vessel and switching modes between performing method I or method II in the reaction vessel wherein no catalyst is present. The reaction vessel may be provided with a burner located at the top of the reaction vessel, the burner may include coaxial channels for the separate introduction of the different gas streams. Method I may be a reverse water gas shift reaction at elevated temperature. Method II may be a partial oxidation reaction at elevated temperature.

Abstract: The present invention relates to a process for converting carbon dioxide and hydrogen by performing a reverse water gas shift reaction at elevated temperature, the process comprising introducing carbon dioxide, hydrogen and oxygen into a reaction vessel having an inlet and an outlet, and, wherein the reverse water gas shift reaction takes place in two different zones of the reaction vessel, being a top zone (z1) adjacent to a bottom zone (z2). The process produces a product stream comprising mainly carbon monoxide, hydrogen and water. The process is useful in reducing the carbon footprint of certain industrial technologies, and in addition, the process is useful in the production of synthesis gas.

Abstract: A process for converting carbon dioxide and hydrogen into a product stream comprising carbon monoxide, water and hydrogen by introducing carbon dioxide, hydrogen and oxygen into a reaction vessel, and performing a reverse water gas shift reaction at elevated temperature, wherein (a) no catalyst is present in vessel (b) gas stream comprising carbon dioxide, a hydrogen and an oxygen rich gas stream are introduced into the vessel in separate feed streams, (c) the hydrogen and oxygen rich gas stream being introduced in close vicinity of each other, via burner comprising coaxial channels wherein gases gas undergo a combustion reaction, providing the heating energy required for the reverse water-gas shift reaction; and (d) the temperature in vessel is in the range of 1000 to 1500° C. by varying the molar ratio of hydrogen to oxygen. It is useful in reducing the carbon footprint of certain industrial technologies, and in production of synthesis gas.

Abstract: The present application provides a method for controlling soot make in a process for the gasification of a liquid carbonaceous feedstock. The gasification process comprises: partially oxidizing the carbonaceous feedstock in a gasifier to produce syngas; guiding the syngas from an outlet of the gasifier to a quench section; cooling the syngas in the quench section to provide cooled syngas; providing the cooled syngas to a soot removal unit; using the soot removal unit to remove solids from the cooled syngas, the soot removal unit providing a cleaned syngas stream and a waste slurry stream comprising the solids removed from the syngas; continuously monitoring a concentration of total suspended solids (TSS) in the waste slurry stream; providing the concentration of total suspended solids (TSS) to a control system. The control system continuously optimizes the gasification process to changes in concentration of total suspended solids, carbon-to-ash ratio, and optional additional parameters.

Abstract: The present application provides a method for controlling soot make in a process for the gasification of a liquid carbonaceous feedstock. The gasification process comprises: partially oxidizing the carbonaceous feedstock in a gasifier to produce syngas; guiding the syngas from an outlet of the gasifier to a quench section; cooling the syngas in the quench section to provide cooled syngas; providing the cooled syngas to a soot removal unit; using the soot removal unit to remove solids from the cooled syngas, the soot removal unit providing a cleaned syngas stream and a waste slurry stream comprising the solids removed from the syngas; continuously monitoring a concentration of total suspended solids (TSS) in the waste slurry stream; providing the concentration of total suspended solids (TSS) to a control system. The control system continuously optimizes the gasification process to changes in concentration of total suspended solids, carbon-to-ash ratio, and optional additional parameters.

Abstract: Process for the preparation of olefins comprising reacting an oxygenate and/or olefinic feed in a reactor in the presence of a molecular sieve catalyst to form a mixture which comprises olefins and at least partially coked catalyst; passing at least partially coked catalyst to a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; separating at least partially regenerated catalyst and at least part of the gaseous mixture; analysing the composition of the gaseous mixture to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting the mass flow rate of the oxygen-containing gas on the basis of the analysis of the gaseous mixture; and passing at least part of the at least partially regenerated catalyst back to the reactor.

Abstract: Process for the preparation of olefins comprising reacting an oxygenate and/or olefinic feed in a reactor in the presence of a molecular sieve catalyst to form a mixture which comprises olefins and at least partially coked catalyst; separating olefins and at least partially coked catalyst as obtained; passing the at least partially coked catalyst to a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; analyzing the at least partially regenerated catalyst to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting one or more conditions of the regeneration of the at least partially coked catalyst on the basis of the analysis of the at least partially regenerated catalyst; and passing the at least partially regenerated catalyst to the reactor.

Abstract: Process for the regeneration of an at least partially coked molecular sieve catalyst comprising introducing the at least partially coked catalyst into a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate at least part of the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; recovering part of the at least partially regenerated catalyst; analysing the at least partially regenerated catalyst to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting one or more conditions of the regeneration of the at least partially coked catalyst on the basis of the analysis of the at least partially regenerated catalyst; and separating at least partially regenerated catalyst and at least part of the gaseous mixture as obtained in step (b).

Abstract: Process for the regeneration of an at least partially coked molecular sieve catalyst comprising introducing the at least partially coked catalyst into a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate at least part of the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; separating at least partially regenerated catalyst and at least part of the gaseous mixture; and analyzing the composition of the gaseous mixture to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting the mass flow rate of the oxygen-containing gas on the basis of the analysis of the gaseous mixture.

Abstract: Process for the preparation of olefins comprising reacting an oxygenate and/or olefinic feed in a reactor in the presence of a molecular sieve catalyst to form a mixture which comprises olefins and at least partially coked catalyst; separating olefins and at least partially coked catalyst as obtained; passing the at least partially coked catalyst to a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; analysing the at least partially regenerated catalyst to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting one or more conditions of the regeneration of the at least partially coked catalyst on the basis of the analysis of the at least partially regenerated catalyst; and passing the at least partially regenerated catalyst to the reactor.

Abstract: Process for the preparation of olefins comprising introducing an oxygenate and/or olefinic feed into a reactor; reacting the oxygenate and/or olefinic feed in the reactor in the presence of a molecular sieve catalyst to form a mixture which comprises olefins and at least partially coked catalyst; separating olefins and at least partially coked catalyst; recovering olefins; and controlling the temperature of the oxygenate and/or olefinic feed to be introduced into the reactor on the basis of the temperature of the mixture formed in the reaction and/or the olefins obtained.

Abstract: Process for the preparation of olefins comprising reacting an oxygenate and/or olefinic feed in a reactor in the presence of a molecular sieve catalyst to form a mixture which comprises olefins and at least partially coked catalyst; passing at least partially coked catalyst to a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; separating at least partially regenerated catalyst and at least part of the gaseous mixture; analysing the composition of the gaseous mixture to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting the mass flow rate of the oxygen-containing gas on the basis of the analysis of the gaseous mixture; and passing at least part of the at least partially regenerated catalyst back to the reactor.

Abstract: Process for the preparation of olefins, which process comprising introducing an oxygenate and/or olefinic feed through introduction means into a reactor; reacting the oxygenate and/or olefinic feed in the reactor in the presence of a molecular sieve catalyst to form a mixture with a resulting gas superficial velocity which mixture comprises olefins and at least partially coked catalyst; separating olefins and at least partially coked catalyst; recovering olefins; and controlling the gas superficial velocity of the mixture at a predetermined level in the reactor on the basis of the inlet mass gas flow rate of the feed.

Abstract: Process for the regeneration of an at least partially coked molecular sieve catalyst comprising introducing the at least partially coked catalyst into a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate at least part of the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; separating at least partially regenerated catalyst and at least part of the gaseous mixture; and analysing the composition of the gaseous mixture to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting the mass flow rate of the oxygen-containing gas on the basis of the analysis of the gaseous mixture.

Abstract: Process for the regeneration of an at least partially coked molecular sieve catalyst comprising introducing the at least partially coked catalyst into a regenerator; introducing into the regenerator an oxygen-containing gas to regenerate at least part of the at least partially coked catalyst, thereby producing a gaseous mixture and at least partially regenerated catalyst; recovering part of the at least partially regenerated catalyst; analysing the at least partially regenerated catalyst to control the burning rate of the coke present on the at least partially coked catalyst in the regenerator by adjusting one or more conditions of the regeneration of the at least partially coked catalyst on the basis of the analysis of the at least partially regenerated catalyst; and separating at least partially regenerated catalyst and at least part of the gaseous mixture as obtained in step (b).