Producing C5 olefins from steam cracker C5 feeds may include reacting a mixed hydrocarbon stream comprising cyclopentadiene, C5 olefins, and C6+ hydrocarbons in a dimerization reactor where cyclopentadiene is dimerized to dicyclopentadiene. The dimerization reactor effluent may be separated into a fraction comprising the C6+ hydrocarbons and dicyclopentadiene and a second fraction comprising C5 olefins and C5 dienes. The second fraction, a saturated hydrocarbon diluent stream, and hydrogen may be fed to a catalytic distillation reactor system for concurrently separating linear C5 olefins from saturated hydrocarbon diluent, cyclic C5 olefins, and C5 dienes contained in the second fraction and selectively hydrogenating C5 dienes. An overhead distillate including the linear C5 olefins and a bottoms product including cyclic C5 olefins are recovered from the catalytic distillation reactor system. Other aspects of the C5 olefin systems and processes, including catalyst configurations and control schemes, are also described.

A process and related system for producing para-xylene (PX). In an embodiment, the process includes (a) separating a feed stream comprising C.sub.6+ aromatic hydrocarbons into a toluene containing stream and a C.sub.8+ hydrocarbon containing stream and (b) contacting at least part of the toluene containing stream with a methylating agent in a methylation unit to convert toluene to xylenes and produce a methylated effluent stream. In addition, the process includes (c) recovering PX from the methylated effluent stream in (b) to produce a PX depleted stream and (d) transalkylating the PX depleted stream to produce a transalkylation effluent stream. The transalkylation effluent stream includes a higher concentration of toluene than the PX depleted stream. Further, the process includes (e) converting at least some ethylbenzene (EB) within the C.sub.8+ hydrocarbon containing stream into toluene and (f) flowing the toluene converted in (e) to the contacting in (b).

A method for the large-scale synthesis of a zeolite-templated carbon (ZTC). The method includes the steps of: introducing a bed material comprising a zeolite to a fluidized bed reactor and heating the bed material to a temperature between 550 C. and 800 C.; fluidizing the bed material with a fluidizing gas and maintaining the temperature of the bed material between 550 C. and 800 C.; introducing an organic carbon precursor while fluidizing the zeolite for a period of time such that carbon is deposited on the zeolite by chemical vapor deposition to produce a zeolite-carbon composite; and treating the zeolite-carbon composite with an acid solution such that the zeolite template is dissolved and the ZTC is obtained.

The present disclosure provides oxidative coupling of methane (OCM) systems for small scale and world scale production of olefins. An OCM system may comprise an OCM subsystem that generates a product stream comprising C.sub.2+ compounds and non-C.sub.2+ impurities from methane and an oxidizing agent. At least one separations subsystem downstream of, and fluidically coupled to, the OCM subsystem can be used to separate the non-C.sub.2+ impurities from the C.sub.2+ compounds. A methanation subsystem downstream and fluidically coupled to the OCM subsystem can be used to react H.sub.2 with CO and/or CO.sub.2 in the non-C.sub.2+ impurities to generate methane, which can be recycled to the OCM subsystem. The OCM system can be integrated in a non-OCM system, such as a natural gas liquids system or an existing ethylene cracker.

A device for making polybutylene terephthalate includes (1) a slurry paste vessel; (2) a tower reactor to which a mixture of 1,4-butane diol and terephthalic acid from vessel (1) is supplied, the tower reactor having a plurality of reactor zones wherein the lower third of the tower reactor is in the form of a hydrocyclone with attached heat exchanger, and the hydrocyclone has a supply line from vessel (1), the hydrocyclone being connected to the top side of the tower reactor; (3) a first continuously stirred tank reactor to which the product from tower reactor (2) is supplied; (4) an optional second continuously stirred tank reactor to which the product from (3) is supplied; (5) a dual shaft ring reactor to which the product from stirred tank reactor (3) or (4), is supplied; and (6) a pelletizer where the product from dual shaft ring reactor (5) is continuously fed and pelletized.

Disclosed are a graphene material production device and a system including the device. The device includes: a first reaction component, a second reaction component and a negative pressure generating component. The first reaction component includes a first reaction chamber and a first material outlet arranged at a bottom of the first reaction chamber. The second reaction component includes a second reaction chamber and a second material inlet. A connecting passage between the first material outlet and the second material inlet is provided with a valve. A suction hole of the negative pressure generating component is provided inside the second reaction chamber. The use of the device in the process of producing a graphene material by a redox method can overcome the problem that the viscous material is difficult to transfer, thereby reducing the production difficulty and effectively improving the production efficiency of graphene materials.

A method and device for lightening heavy oil by utilizing a suspension-bed hydrogenation process are provided. In the process, a part of a raw oil is mixed with a suspension-bed hydrocracking catalyst to form a first mixture, then the first mixture is subjected to first shear and second shear in sequence so as to realize high dispersion and mixing of the catalyst and the raw oil; through pretreatment of the raw oil, the device can prevent the raw oil from coking in the hydrogenation process; through the adoption of a suspension-bed reactor with a liquid phase self-circulation function or a cold-wall function; and light and heavy components are separated from the suspension-bed hydrogenated product in advance and only medium component is subjected to fixed-bed hydrogenation, thereby reducing the load of the fixed-bed hydrogenation, prolonging the service life of the fixed-bed catalyst, improving the yield and quality of gasoline and diesel, and being beneficial for energy conservation and emission reduction of the whole system.

The present invention provides methods for decomposing and extracting compositions for the recovery of petroleum-based materials from composites comprising those petroleum-based materials, comprising subjecting the compositions and/or composites to microwave radiation, wherein the microwave radiation is in the range of from about 4 GHz to about 18 GHz. The present invention also provides for products produced by the methods of the present invention and for apparatuses used to perform the methods of the present invention.

Combustion gas of an internal combustion engine passes through an exhaust system to an outlet opening. A detection device generates a state signal that describes an engine noise of the internal combustion engine. A control apparatus actuates at least one loudspeaker to produce a sound at the outlet opening based on the state signal to compensate for the engine noise or produce another engine noise, independently of the state signal based on predetermined audio data and thereby to use the at least one loudspeaker to audibly output an advisory signal described by the audio data.

An integrated process for production of urea and urea-ammonium sulphate (UAS) comprises: a urea synthesis step carried out in a urea synthesis reactor; a recovery and concentration step, wherein a urea solution produced in the urea synthesis step is progressively concentrated in at least one recovery section and in a concentration section, recovering unreacted ammonia and carbon dioxide and water from said urea solution; a step of producing ammonium sulphate by reaction of sulphuric acid and ammonia in an ammonium sulphate production apparatus; a step of mixing said ammonium sulphate with concentrated urea coming from the concentration section to produce a UAS mixture; in the ammonium sulphate production step, at least a part of the ammonia is provided by at least one off-gas containing ammonia and recovered from the recovery and concentration step.