Abstract:
An object of the present invention is to provide, for the production of isobutene, a high-yielding, highly-selective, and long-term stable production process of isobutene from TBA. With respect to the production of TBA, an object of the present invention is to provide a TBA production process in which, through long-term stable maintenance of a high reaction activity, long-term continuous operation is enabled and the productivity is improved. The present invention discloses a process for producing isobutene that employs a dehydration temperature of from 200 to 450° C. in use of an alumina catalyst that contains a Na content of 0.6% by weight or less in terms of NaO2 and a Na content of 0.4% by weight in terms of NaO2, and has a specific surface area of from 200 to 600 m2/g.
Abstract:
A static devolatilisation apparatus (1) adapted for devolatilising a viscous liquid (2) comprising a volatile component is disclosed. The apparatus (1) comprises a phase separation chamber (100) in an upper region (5) for treating the viscous liquid (2) in a first devolatilisation step to form a first devolatilised viscous liquid (21), and a distributor sub-unit 200 is located below the phase separation chamber (100) and above a lower sump region (4). The sub-unit (200) has a second discharge region (222) embodied such that it is contacted by the first devolatilised viscous liquid (21), and the region (222) has a surface (223) embodied such that the first devolatilised viscous liquid (21) is treated in a second devolatilisation step. The present invention further relates to a process to devolatilising a viscous liquid using the apparatus (1) and also to the use of the apparatus (1) in the devolatilisation of polymer melt or solution.
Abstract:
Disclosed is a method of increasing the capacity of an existing urea plant. With reference to the regular components of a urea plant, including a synthesis section comprising a high pressure carbamate condenser and a reactor, and a recovery section, the method comprises installing an additional reactor between the recovery section and the high pressure carbamate condenser. The additional reactor is preferably installed in connection with an ejector, so as to allow ground placement of the additional reactor.
Abstract:
A process for the direct synthesis of urea from ammonia and carbon dioxide with increased corrosion resistance, comprising, in the high-pressure synthesis section, a reaction step in a vertical reactor fed with at least one stream of fresh carbon dioxide containing a passivating agent and a decomposition-stripping step of the non-converted reagents, wherein the gas-liquid mixture collected at the head of the reactor is separated into a gaseous stream and a liquid stream fed to the tail and head of the stripper, respectively.
Abstract:
A carboxylic acid e.g. acetic acid, is recovered from an aqueous feed stream containing the corresponding ester, an alcohol and a small amount of water by catalytically dehydrating the alcohol to the corresponding ether and water, and reacting the water with the ester to generate a liquid carboxylic acid rich product stream. The acid is recovered by distillation. In a second embodiment, additional alcohol and/or water are co-fed with the feed or fed directly to a catalytic distillation column, resulting in a liquid bottom product stream of substantially pure acetic acid and a top distillate stream of substantially pure ether.
Abstract:
A process and apparatus for recycling LCO and/or HCO to a hydroprocessing zone to saturate aromatics for cracking in an FCC unit is disclosed. The recycle cracked stream may be recycled to a downstream hydroprocessing zone to avoid a first hydroprocessing zone that is primarily for demetallizing (and desulfurizing) feed to the FCC unit.
Abstract:
A method for producing allyl alcohol is disclosed. The method includes steps of feeding allyl acetate and water into a reactive distillation column; performing a reaction in a reaction zone and separating a product containing allyl alcohol, acetic acid and water from the reactive distillation column. Accordingly, the method effectively enhances a conversion rate of hydrolysis for allyl acetate, simplifies the process and reduces energy consumption.
Abstract:
Processes for isolating 1,1,1,2,3-pentachloropropane from a crude product stream containing the 1,1,1,2,3-pentachloropropane and ferric chloride. The processes may include deep distillation of the crude, treatment of the crude with a reagent that deactivates the ferric chloride followed by distillation on the deactivated crude stream, aqueous washing of the crude product stream to remove ferric chloride followed by distillation on the deactivated crude stream. Other embodiments simultaneously prepare 1,1,2,3-tetrachloroprene and 1,1,1,2,3-pentachloroprane.
Abstract:
The present invention provides a method for simultaneous production of components suitable for production of base oil and fuel components. In the method a feedstock comprising fatty acids and/or fatty acid esters is entered into a reaction zone and subjected to a ketonisation reaction in the presence of a dual catalyst system. This system is configured to perform a ketonisation reaction and a hydrotreatment reaction, under hydrogen pressure. Subsequently ketones are obtained.
Abstract:
The present invention provides a method for simultaneous production of components suitable for production of base oil and fuel components. In the method a feedstock comprising fatty acids and/or fatty acid esters is entered into a reaction zone and subjected to a ketonization reaction in the presence of a dual catalyst system. This system is configured to perform a ketonization reaction and a hydrotreatment reaction, under hydrogen pressure. Subsequently ketones are obtained.