A device for converting cellulose to sugar has a reaction chamber with a plurality of control components, and a control assembly. The control assembly is operatively connected to the reaction chamber, a drive assembly and control components to transmit and receive interoperability signals. The device has an inlet hopper with a detector, a crusher, an outlet hopper, a sensor assembly, a steam inlet, and a carbon dioxide inlet. The inlet hopper is configured to receive and analyze proportion data of matters in a feedstock and catalyst mixture via the detector. The crusher receives and grinds the mixture from the inlet hopper to induce chemical reaction for producing sugar. The outlet hopper is configured to determine a proportion data of matter in the grinded mixture. The control assembly is configured to determine adjustments need to be performed on the components and drive assembly to optimize the sugar production.

A steam methane reformer (SMR) system includes an outer tube, wherein a first end of the outer tube is closed; an inner tube disposed in the outer tube, wherein a first end of the inner tube is open. A flow channel is defined within the inner tube and an annular space is defined between the outer tube and the inner tube, the flow channel being in fluid communication with the annular space. The SMR system includes a catalytic foam disposed in the annular space between the outer tube and the inner tube, the catalytic foam comprising a catalyst.

A built-in micro interfacial enhanced reaction system and process for PTA production with PX are provided. The system includes a reactor and a micro interfacial unit disposed inside reactor. The reactor includes a shell, an inner cylinder concentrically disposed inside shell, and a circulating heat exchange device partially disposed outside shell, inner cylinder having a bottom end connected to inner bottom surface of the shell in closed manner and an open top end, a region between shell and inner cylinder being first reaction zone, inner cylinder containing second reaction zone and third reaction zone from top to bottom, circulating heat exchange device being connected to inner cylinder and micro interfacial unit respectively. The invention can solve problems of large waste of reaction solvent acetic acid under high temperature and high pressure and being unable to take out the product TA in time during existing process of PTA production with PX.

The process and apparatus of the disclosure utilize a heater between a hydroprocessing reactor and a hydroisomerization reactor. A hydroprocessing feed exchanger cools hydroprocessed effluent to effect turndown of heated hydroprocessed effluent so as to not feed the hydroprocessed effluent to the hydroisomerization reactor at a higher temperature than necessary.

The present invention relates to a plant for oligomerizing ethylene to produce oligomerized alpha-olefins, with production of a fouling by-product in the form of a deposit, said plant comprising a reaction section comprising: —a reactor (c) for two-phase gas/liquid or single-phase all-liquid oligomerization proceeding from an optional solvent, an oligomerization catalyst and ethylene, and —cooling means associated with said reactor in the form of at least one cooling circuit external to the reactor and/or in the form of a jacket of the walls of the reactor. Packings are disposed in the reaction section in order to increase the contact surface area per unit volume that is accessible to the deposition of the byproduct.

A process for producing bis(fluorosulfonyl) imide includes providing a solution comprising fluorosulfonic acid and urea, the solution maintained at a solution temperature from about 0° C. to about 70° C.; reacting the solution in the presence of a reaction medium at a reaction temperature from 80° C. to about 170° C. to produce a product stream including bis(fluorosulfonyl) imide, ammonium fluorosulfate and the reaction medium; separating the ammonium fluorosulfate from the product stream to produce an intermediate product stream; and separating the intermediate product stream into a concentrated product stream and a first recycle stream, the concentrated product stream including a higher concentration of bis(fluorosulfonyl) imide than the first recycle stream.

Techniques for converting carbonate material to carbon monoxide include transferring heat and at least one feed stream that includes a carbonate material and at least one of hydrogen, oxygen, water, or a hydrocarbon, into an integrated calcination and syngas production system that includes a syngas generating calciner (SGC) reactor; calcining the carbonate material to produce a carbon dioxide product and a solid oxide product; initiating a syngas production reaction; producing, from the syngas production reaction, at least one syngas product that includes at least one of a carbon monoxide product, a water product or a hydrogen product; and transferring at least one of the solid oxide product or the at least one syngas product out of the SGC reactor.

Process for cracking hydrocarbon gases, wherein the hydrocarbon gas is passed through a flow channel of an absorptive receiver reactor (1, 30, 40), characterized in that cracking takes place during the passing through the receiver reactor (1, 30, 40), wherein in a first region (21) of the flow channel (2) the hydrocarbon gas is heated to its cracking temperature, in an adjoining second, downstream flow region (22) is heated to beyond its cracking temperature and in a third, further downstream region (23) of the flow channel is heated yet further and is brought therein into physical contact, over the cross-section of said region, with a reaction accelerator, after which the stream of products downstream of the reaction accelerator is discharged from the receiver reactor (1, 30, 40), and wherein the heating of the hydrocarbon gas to above its cracking temperature is achieved by absorption of blackbody radiation (20) which is given off by the reaction accelerator heated by solar radiation (7) incident thereupon to the hydrocarbon gas flowing towards it, in such a way that the hydrocarbon gas in the flow channel (2) and extending up to the reaction accelerator forms disc-shaped, consecutive temperature zones (60 to 67) of ever-increasing temperature extending transversely to the flow channel (2).

Provided is a method of preparing a diester-based material, more particularly, a method of preparing a diester-based material, which is carried out by a continuous preparation process of a diester-based material including a reaction part in which a total of n reaction units from a first reaction unit to an nth reaction unit are connected in series, the reaction unit including a reactor which esterifies dicarboxylic acid and alcohol, including: esterifying dicarboxylic acid and alcohol in a reactor of the first reaction unit to produce a reaction product, and supplying a lower discharge stream including the reaction product to a reaction unit at a rear end through a lower discharge line; and supplying a liquid material through a liquid supply line connected to a lower discharge line of the reactor of the first reaction unit.

Embodiments of the present disclosure are directed to a diesel reformer system comprising: a diesel autothermal reforming unit; a post-reforming unit disposed downstream of the autothermal reforming unit; a heat exchanger disposed downstream of the post-reforming unit; and a desulfurization unit disposed downstream of the heat exchanger.