A chemical plant or a petrochemical plant or a refinery may include one or more pieces of equipment that process one or more input chemicals to create one or more products. For example, catalytic dehydrogenation can be used to convert paraffins to the corresponding olefin. A delta temperature controller may determine and control differential temperature across the reactor, and use a delta temperature to control a set point for a heater temperature controller. By doing so, the plant may ramp up a catalytic dehydrogenation unit faster and ensure it does not coke up the catalyst and/or foul a screens too quickly. Catalyst activity may be taken into account and allow the plant to have better control over production and run length of the unit.

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.

Control methods are disclosed for continuous, unmodulated, multiple catalytic conversion step processes using at least two catalysts, a first catalyst and a second catalyst, that accommodate changes in the performance of each catalyst and the relative performances of the catalysts. In the methods, certain process parameters are used in a manner that is indicative of changes in catalyst performance, and the control methods provide for adjustment of at least one of: the absolute amount of catalytically active species and relative amounts of each of the first catalyst and second catalyst and at least one of the rate of feed or concentration of the raw material to the reaction zone.

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.

Processes for the production of high purity isobutylene are disclosed. The processes may include supplying a mixed C4 feed stream to a catalytic distillation column, which may contain a butene isomerization catalyst. 1-butene is isomerized to 2-butene and concurrently in the catalytic distillation column the 2-butene is separated from the isobutane and isobutylene. The overheads fraction comprising the isobutane and isobutylene is then condensed in an overheads system and fed to a splitter, where the isobutane is separated from the isobutylene. The process further includes operating the catalytic distillation column at an overheads temperature greater than a bottoms temperature of the splitter, and heating a portion of the splitter bottoms stream via indirect heat exchange with at least a portion of the catalytic distillation column overheads fraction, thereby producing a heated bottoms stream (reboil vapor) fed to the splitter and a cooled overheads fraction.

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.

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.

A method of producing an organic peroxide includes introducing an organic solution and a peroxide solution into a mixing tank to form a mixture. The method further includes circulating the mixture over a fixed catalyst bed to form the organic peroxide and measuring a concentration of the organic peroxide in the mixture. Further, the method includes removing at least a portion of the mixture when the concentration reaches a set value.

A process for preparing a polyurethane polymer comprises the step of: I) mixing a first component (100) comprising a polyisocyanate with a second reactant component (200) comprising a compound having Zerewitinoff-active hydrogen atoms in a mixing vessel (300) to obtain a reaction mixture (400), wherein the first reactant component (100) and/or the second reactant component (200) are contacted with a catalyst bed (500) before they are mixed in the mixing vessel (300) and/or the reaction mixture (400) is contacted with a catalyst bed (500), wherein the catalyst bed (500) contains a catalyst reversibly sorbed on a substrate, the catalyst catalyses the reaction of isocyanate groups with themselves or with Zerewitinoff-active compounds and the catalyst is released into the first component (100), second component (200) or reaction mixture (400) that is in contact with the catalyst bed (500), such that a reaction mixture (410) containing the catalyst is obtained.

The present disclosure relates to methods for controlling gas phase polymerization reactors. A method for controlling a fluidized bed reactor can include forming a fluidized bed in a reactor followed by discharge of polymer product from the reactor to a product discharge tank. The polymer product can then be discharged from the product discharge tank to a blow tank and the pressure of the blow tank is measured. The pressure measured in the blow tank can then be used to control the reactor by changing one or more reactor operating inputs based on the measured blow tank pressure.