The present invention relates to a process for the continuous preparation of a polyolefin from one or more α-olefin monomers in a reactor system, the process for the continuous preparation of polyolefin comprising the steps of: feeding a polymerization catalyst to a fluidized bed through an inlet for a polymerization catalyst; feeding the one or more monomers to the reactor, polymerizing the one or more monomers in the fluidized bed to prepare the polyolefin; withdrawing polyolefin formed from the reactor through an outlet for polyolefin; withdrawing fluids from the reactor through an outlet for fluids and transporting the fluids through first connection means, an heat exchanger to cool the fluids to produce a cooled recycle stream, and through second connection means back into the reactor via an inlet for the recycle stream; wherein a thermal run away reducing agent (TRRA) is added to the reactor in a discontinuous way.

A method for producing (meth)acrolein by vapor-phase catalytic oxidation of propylene or isobutylene in a multitubular reactor including a plurality of reaction tubes, the reaction tubes each including a reaction zone filled with a catalyst including molybdenum oxide and a cooling zone filled with an inert substance, wherein a temperature of a heat medium that flows outside the cooling zone is lower than a temperature of a heat medium that flows outside the reaction zone, and wherein the inert substance includes an inert substance having a major-axis length that is equal to or more than 1.7 times a major-axis length of the catalyst. A method for producing (meth)acrylic acid in which (meth)acrolein thus produced is converted to (meth)acrylic acid by vapor-phase catalytic oxidation.

An ultra-low-speed rotating low-strain high-filling-rate hydrogen alloy automatic absorption-desorption reaction device includes a shell, a hydrogen storage reaction bed, a motor, a controlling and monitoring system, a wire inlet port, a hydrogen absorption and desorption port, and a universal angle wheel. The reaction bed is circular, rotating at a low speed under driving of a light ultra-low speed motor; facades on two sides of the reaction bed are respectively provided with a transmission shaft and the hydrogen absorption and discharge port which are respectively connected with an ultra-low-speed gear reduction motor or a high-pressure hydrogen storage tank and a hydrogen-consuming device; the reaction bed includes a hydrogen storage metal alloy, a heat-conducting anti-hardening filling material, and a phase change material; a shell of the alloy reaction bed has a heater and an external side surface of a hydrogen storage alloy reaction device has a PLC controlling and monitoring system.

Incorporating into a fixed bed reactor for an exothermal reaction having a catalyst supported on a support having a thermal conductivity typically less than 30 W/mk within the reaction temperature control limits heat dissipative particles having a thermal conductivity of at least 50 W/mk less than 30 W/mk within the reaction temperature control limits helps control the temperature of the reactor bed.

A process for large scale and energy efficient production of oxygenates from sugar is disclosed in which a sugar feedstock is introduced into a thermolytic fragmentation reactor comprising a fluidized stream of heat carrying particles which are separated from the reaction product and directed to a reheater comprising a resistance heating system.

A process for producing 2,3,3,3-tetrafluoropropene comprises the steps: i) in a first adiabatic reactor comprising a fixed bed composed of an inlet and an outlet, bringing 2-chloro-3,3,3-trifluoropropene into contact with hydrofluoric acid in the gas phase in the presence of a catalyst to produce a stream A comprising 2,3,3,3-tetrafluoropropene, HF and unreacted 2-chloro-3,3,3-trifluoropropene; and ii) in a second adiabatic reactor comprising a fixed bed composed of an inlet and an outlet, bringing hydrofluoric acid into contact in the gas phase, optionally in the presence of a catalyst, with at least one chlorinated compound to produce a stream B comprising 2-chloro-3,3,3-trifluoropropene. The stream A obtained in step i) feeds said second reactor. The inlet temperature of the fixed bed of one of said first or second reactors is between 300° C. and 400° C. The longitudinal temperature difference between the inlet and the outlet of the fixed bed in question is less than 20° C.

The invention relates to hydrocarbon conversion, to equipment and materials useful for hydrocarbon conversion, and to processes for carrying out hydrocarbon conversion, e.g., hydrocarbon pyrolysis processes. The hydrocarbon conversion is carried out in a reactor which includes at least one channeled member that comprises refractory and has an open frontal area≤55%. The refractory can include non-oxide ceramic.

Systems and methods are provided for refining crude oils and/or other broad boiling range feedstocks to form fuels. A flash separation can be used to separate the feed into a lower boiling fraction and a higher boiling fraction. After the flash separation, the higher boiling portion is passed into a pyrolysis reactor for conversion of higher boiling compounds and formation of light olefins. The lower boiling fraction can be combined with the resulting pyrolysis effluent as a quench stream. The combined, partially pyrolyzed stream can then be passed into an olefin oligomerization process to convert the olefins formed during pyrolysis into naphtha and/or diesel boiling range compounds. After the olefin oligomerization process, one or more separations can be performed to generate various fractions, including but not limited to a naphtha fraction, a distillate fuel fraction, a fuel oil fraction, a light hydrocarbon recycle stream, and a CO.sub.2-containing stream. Optionally, the naphtha fraction, the distillate fraction, and/or the fuel oil fraction can be hydrotreated.

A method of producing liquid fuel and/or chemicals from a carbonaceous material entails combusting a conditioned syngas in pulse combustion heat exchangers of a steam reformer to help convert carbonaceous material into first reactor product gas which includes carbon monoxide, hydrogen, carbon dioxide and other gases. A portion of the first reactor product gas is transferred to a hydrogen reformer into which additional conditioned syngas is added and a reaction carried out to produce an improved syngas. The improved syngas is then subject to one or more gas clean-up steps to form a new conditioned syngas. A portion of the new conditioned syngas is recycled to be used as the conditioned syngas in the pulse combustion heat exchangers and in the hydrocarbon reformer. A system for carrying out the method include, a steam reformer, a hydrocarbon reformer, first and second gas-cleanup systems, a synthesis system and an upgrading system.

A reactor (1) for thermochemical reactions is provided comprising a reactor shell (13) having an inlet (2) and an outlet (3). Solid catalyst (16) is provided in reaction zones (4a, 4b, 4c) in which at least a portion of reactants entering the reactor (1) undergo a thermochemical reaction. A heat exchange medium is provided in heat exchange zones such that heat is exchanged between the reaction zones (4a, 4b, 4c) and the heat exchange medium. One or more hollow inserts (11) at least partially extend through the reaction zones (4a, 4b, 4c). The hollow inserts (11) are configured to form a flow path to either: divert a portion of the reactants from the reactor inlet (2) or from one reaction zone to a different reaction zone; or divert a portion of the heat exchange medium from one heat exchange zone to a different heat exchange zone.