A process for the selective dimerization and etherification of isoolefins. The process including feeding a mixed C5 stream to a selective hydrogenation unit to convert dienes to olefins and isoolefins, producing a hydrogenated effluent stream. The hydrogenated effluent stream is fed to a first fixed bed reactor, producing a first reactor effluent. The first reactor effluent is fed to a catalytic distillation reactor system, producing a first overheads including unreacted olefins, isoolefins, oxygenate, and one or more C5 ethers and a first bottoms including dimers of the isoolefins, any produced trimers of the isoolefins, and heavy oxygenates. The first overheads is fed to a second fixed bed reactor, producing a second reactor effluent including dimers of the isoolefins, unreacted C5s, and unreacted oxygenates. The first bottoms stream and the second reactor effluent are combined and fed to a product splitter, producing a second overheads stream including unreacted C5 olefins, isoolefins, and oxygenates and a second bottoms stream including C10+ hydrocarbons.

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 system for generating hydrogen includes an ammonia decomposition bed configured to introduce an ammonia gas, decompose the ammonia gas into a high-pressure first mixed gas including nitrogen and hydrogen, and discharge the high-pressure first mixed gas; an ammonia adsorption bed supplied with the high-pressure first mixed gas from the ammonia decomposition bed, and configured to adsorb ammonia of the first mixed gas, and discharge a high-pressure second mixed gas including nitrogen and hydrogen; and a nitrogen adsorption bed directly supplied with the high-pressure second mixed gas from the ammonia adsorption bed, and configured to adsorb the nitrogen, and discharge the hydrogen.

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.

An object of the present invention is to provide a method for producing an unsaturated carboxylic ester, wherein the risk of polymerization blockage is reduced and the required equipment cost and workload involved are kept low while maintaining a high conversion rate in an esterification reaction of unsaturated carboxylic acid. This object can be achieved by a method for producing an unsaturated carboxylic ester, which includes performing an esterification reaction using a reactor packed with a solid catalyst, wherein unsaturated carboxylic acid and alcohol are continuously fed to the reactor from an inlet thereof to form a fluid of the reaction solution in the reactor, and the vaporized organic solvent is continuously fed to the reactor from the inlet or a part near the inlet of the reactor.

A method for controlling temperature of a chemical reaction without measuring a temperature of the chemical reaction. Changes in mass of a chemical reaction are monitored and are used to calculate the temperature of the system. The reaction can be maintained at a desired temperature (T) without measuring the temperature. The disclosed method is useful for reactions that occur at non-equilibrium conditions where any measured temperature would presume steady-state conditions.

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.

The invention relates to a process and a plant for producing methanol from an input gas including carbon monoxide and hydrogen using a pre-reactor stage and a main reactor stage. Input gas produced at and under elevated pressure is initially introduced into a pre-reactor stage for catalytic conversion into a first methanol-containing product stream. After separation of methanol from the first methanol-containing product stream and discharging from the pre-reactor stage a remaining gas stream is introduced into a main reactor stage as a residual gas stream after compression to reaction pressure for catalytic conversion into a second methanol-containing product stream, After separation from the second methanol-containing product stream methanol is discharged from the main reactor stage. Using an input gas having a carbon monoxide content of 25% to 36% by volume results in large savings in respect of the compressor output required for the production process.

The invention involves a scale collection device that is located within downflow reactor head for removing solids from feed streams to increase reactor operating cycle time without impact on effective reactor space for catalyst loading and reactor pressure drop. More particularly, a scale collection device is in an upper portion of a reactor vessel above a rough liquid distribution tray and a vapor-liquid distribution tray.

A process for producing one or more of benzene, toluene, or mixed xylenes may include combining one or more aromatic feed chemicals, one or more aromatic-based polymers, hydrodearylation catalyst, and hydrogen in a hydrodearylation unit to form a chemical product. The process may also include passing the chemical product out of the hydrodearylation unit, where the chemical product comprises one or more of benzene, toluene, and mixed xylenes. Additionally, a system for producing one or more of benzene, toluene, or mixed xylenes may include a mixing unit and a hydrodearylation unit. An aromatic feed stream and an aromatic-based polymer stream may be in fluid communication with a mixing unit. A mixing unit effluent stream may be in fluid communication between the mixing unit and the hydrodearylation unit. A chemical product stream may be in fluid communication with the hydrodearylation unit.