The present invention relates to an advanced process control system (APC) for a continuous catalytic regeneration reformer with master-slave configuration to control coke on spent catalyst while maximizing heavy reformate octane barrel using online inferential, both for coke content of spent catalyst and octane of heavy reformate. Further, the present invention relates to provide an APC system for a continuous catalytic regeneration reformer with master-slave configuration, which comprises of a master APC, a reactor APC, and a regenerator APC, wherein, the reactor APC and the regenerator APC are linked to the master APC.

By this invention processes are provided for the conversion of carbohydrate to ethylene glycol by retro-aldol catalysis and sequential hydrogenation using control methods having at least one of acetol (hydroxyacetone) and a tracer as inputs.

Provided is a system and method for producing and purifying biodiesel. In particular, the system comprises a tandem arrangement of at a modular biodiesel reactor and a continuous flow separation and purification unit. The system can further comprise an evaporation unit that is placed between the biodiesel reactor and the continuous flow separation and purification unit.

A support structure for a structured catalytic packing is disclosed. The support structure is in a fixed position relative to the reactor tube containing it. It supports catalyzed casings that are free to move relative to the support structure. The support structure and casings are inserted in the reactor tube such that the support structure is located proximate the longitudinal axis of the tube and the casings are located between the support structure and the reactor tube wall. The support structure comprises a central support tube or rod proximate to, and impervious or perforated discs perpendicular to, the longitudinal axis of the reactor tube, and may comprise spacers separating the discs.

Provided are a method for the catalytic conversion of hydrocarbons with a downer reactor and a device thereof. The specific process of the method is as follows: a raw material of hydrocarbons after being pre-heated (or not) and a low-temperature regenerant from a regenerant cooler entering an entry end of a downer reactor, flowing down along the reactor for reactions such as catalytic cracking, and a mixture of a reactive oil and gas and a catalyst descending to the end of the reactor for rapid separation, thereby achieving the rapid separation of the catalyst and the oil and gas. The main operation conditions thereof are as follows: the reaction temperature is 460 to 680° C., the reaction pressure is 0.11 to 0.4 MPa, the contact time is 0.05 to 2 seconds, and the weight ratio of the catalyst to the raw material (a catalyst-to-oil ratio) is 6 to 50. The separated catalyst to be regenerated (abbreviated as a spent agent) is stripped by means of a stripper, and enters a regenerator and is burned for regeneration, wherein the regeneration temperature is controlled at 630-730° C. The regenerant from the regenerator enters the regenerant cooler to be cooled to 200-720° C., and then enters the downer reactor for recycling

A process for converting post-explosion gases of an inhabitable level, low-oxygen ambient environment to a breathable mixture for human consumption comprises receiving a flow of post-explosion gas with oxygen, carbon dioxide, carbon monoxide, nitrogen, and methane. The oxygen, carbon monoxide, and carbon dioxide are removed from the from the flow of post-explosion gas to create both a mixture including oxygen, carbon monoxide, and carbon dioxide; and a residual stream including nitrogen and methane. The oxygen is removed from the mixture of oxygen, carbon monoxide, and carbon dioxide, and concentrated in a primary oxygen storage canister. The nitrogen is removed from the residual stream and stored in a nitrogen storage canister separate from the oxygen storage canister. The methane is vented back to the inhabitable level, low-oxygen ambient environment. The stored oxygen and nitrogen are metered through a breathing mask at a habitable level of 19-21% oxygen to a user.

New/fresh catalyst is added to a dehydrogenation unit and aged catalyst is removed from the dehydrogenation unit on a continuous or semi-continuous basis while the dehydrogenation unit is in operation. The conversion achieved by the higher activity catalyst results in the production rate of olefin product being maintained at near start-of-run production for longer, with a slower rate of decline. The higher activity catalyst extends run time, reduces feed consumption for each unit of olefin product, and minimizes fresh catalyst expenses.

The present specification relates to a method comprising: (A) mixing a ferrite-based catalyst molded article with diluent material particles; and (B) adding the mixture to a catalyst reactor, and a method for preparing butadiene using the same.

The present invention is directed to methods of producing THC from CBD utilizing non-harsh methodology and resulting in substantially increased yields, as well as devices built upon these novel methods. The methods and devices are material efficient, and in certain embodiments, solvent-free. In particular, in certain embodiments, these methods and related devices are suitable for commercial production of THC from CBD. Furthermore, in certain embodiments, the present invention provides methods of producing THC from CBD in manner that affords tunability to select the ratio of THC-8 to THC-9.

The present invention relates to a micro-interface strengthening reaction system and method for heavy oil hydrogenation preparation of ship fuel, including a liquid phase feed unit, a gas phase feed unit, a micro-interface generator, a fixed-bed reactor and a separation tank. The present invention may reduce the pressure during the reaction by 10-80% while ensuring the efficiency of the reaction by breaking the gas to form micro-sized micro-bubbles and making the micro-bubbles mix with heavy oil to form an emulsion to increase the area between the gas and the liquid phase and to achieve the effect of enhancing mass transfer in a lower preset range. And, the present invention greatly enhances the mass transfer, so that the gas-liquid ratio can be greatly reduced. Also, the method of the present invention has low process severity, high production safety, low product cost per ton, and strong market competitiveness.