A method for cleaning a coke deposit from an internal surface of a process equipment, comprising removing at least a portion of the coke deposit from the internal surface using a flexible pig comprising a plurality of bristles, without damaging a metal protective layer of the internal surface of the process equipment. A flexible pig for cleaning a coke deposit from an internal surface of a process equipment without damaging a metal protective layer of the internal surface, comprising a flexible body formed of a polymeric material, and a plurality of bristles partially encapsulated by the polymeric material of the flexible body.

The present application relates to a selective distillation apparatus and a distillation method, which provides a distillation apparatus capable of switching between a serial connection mode and a parallel connection mode on the situation, thereby enabling selective operation of high-efficiency operation and high-capacity operation.

A plant or refinery may include equipment such as reactors, heaters, heat exchangers, regenerators, separators, or the like. Types of heat exchangers include shell and tube, plate, plate and shell, plate fin, air cooled, wetted-surface air cooled, or the like. Operating methods may impact deterioration in equipment condition, prolong equipment life, extend production operating time, or provide other benefits. Mechanical or digital sensors may be used for monitoring equipment, and sensor data may be programmatically analyzed to identify developing problems. For example, sensors may be used in conjunction with one or more system components to detect and correct maldistribution, cross-leakage, strain, pre-leakage, thermal stresses, fouling, vibration, problems in liquid lifting, conditions that can affect air-cooled exchangers, conditions that can affect a wetted-surface air-cooled heat exchanger, or the like. An operating condition or mode may be adjusted to prolong equipment life or avoid equipment failure.

A plant or refinery may include equipment such as reactors, heaters, heat exchangers, regenerators, separators, or the like. Types of heat exchangers include shell and tube, plate, plate and shell, plate fin, air cooled, wetted-surface air cooled, or the like. Operating methods may impact deterioration in equipment condition, prolong equipment life, extend production operating time, or provide other benefits. Mechanical or digital sensors may be used for monitoring equipment, and sensor data may be programmatically analyzed to identify developing problems. For example, sensors may be used in conjunction with one or more system components to detect and correct maldistribution, cross-leakage, strain, pre-leakage, thermal stresses, fouling, vibration, problems in liquid lifting, conditions that can affect air-cooled exchangers, conditions that can affect a wetted-surface air-cooled heat exchanger, or the like. An operating condition or mode may be adjusted to prolong equipment life or avoid equipment failure.

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.

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.

The invention relates to a method for investigating process streams comprising five or more different hydrocarbon-containing components. In the method at least one process flow line (35) is in operative connection with an online IR spectrometer (2) and an online gas chromatograph (1). The process stream passed through the process stream conduit (35) is subjected to an online characterization which comprises measurements both with the online IR spectrometer and with an online gas chromatograph. The spectral data and the chromatography data are mathematically related to one another by suitable statistical models, thus allowing training of a model used for evaluating the analytical data and for characterizing the process streams. The method according to the invention is characterized by short measurement times in the range of seconds and milliseconds and a high accuracy. The method according to the invention for investigating process streams preferably relates to investigation of process streams deriving from processes proceeding in parallel, the process streams preferably deriving from reaction spaces arranged in parallel.

Methods of transforming a hydrocarbon feedstream into an aromatization product in a multi-stage reverse flow reactor (RFR) apparatus are disclosed. The methods include at least two reaction stages in series, at least one being a pyrolysis stage and at least another being a catalytic aromatization stage. Using a highly saturated hydrocarbon feedstream the pyrolysis stage focuses on desaturation, while the catalytic aromatization stage focuses on aromatization. The catalytic aromatization stage contains a aromatization catalyst that can include substantially no magnesium, scandium, yttrium, titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, manganese, rhenium, iron, ruthenium, cobalt, rhodium, nickel, palladium, platinum, copper, silver, gold, gallium, indium, tin, lanthanides, or actinides, or, in some cases, substantially no added active metals at all. The aromatization product can contain at least 35 mol % aromatic hydrocarbons, based on a total amount of hydrogen and hydrocarbons in the aromatized hydrocarbon product.

Methods of transforming a hydrocarbon feedstream into an aromatization product in a multi-stage reverse flow reactor (RFR) apparatus are disclosed. The methods include at least two reaction stages in series, at least one being a pyrolysis stage and at least another being a catalytic aromatization stage. Using a highly saturated hydrocarbon feedstream the pyrolysis stage focuses on desaturation, while the catalytic aromatization stage focuses on aromatization. The catalytic aromatization stage contains a aromatization catalyst that can include substantially no magnesium, scandium, yttrium, titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, manganese, rhenium, iron, ruthenium, cobalt, rhodium, nickel, palladium, platinum, copper, silver, gold, gallium, indium, tin, lanthanides, or actinides, or, in some cases, substantially no added active metals at all. The aromatization product can contain at least 35 mol % aromatic hydrocarbons, based on a total amount of hydrogen and hydrocarbons in the aromatized hydrocarbon product.

Process and apparatus for producing a naphtha stream is provided. The process comprises providing a kerosene stream to a hydrocracking reactor. The kerosene stream is hydrocracked in the presence of a hydrogen stream and a hydrocracking catalyst in the hydrocracking reactor at hydrocracking conditions comprising a hydrocracking pressure, a hydrocracking temperature, and a liquid hourly space velocity at a net conversion of at least about 90%, to provide a hydrocracked effluent stream comprising liquefied petroleum gas, heavy naphtha fraction and light naphtha fraction. One or more of the hydrocracking conditions are adjusted to maintain a ratio of the light naphtha fraction to the heavy naphtha fraction of at least about 2 by weight, suitably at least about 2.2 and preferably at least about 2.5 in the hydrocracked effluent stream while maintaining the net conversion of at least about 90%.