A system for continuously treating recycled polymeric material includes a hopper configured to feed the recycled polymeric material into the system. An extruder can turn the recycled polymeric material in a molten material. In some embodiments, the extruder uses thermal fluids, electric heaters, and/or a separate heater. The molten material is depolymerized in a reactor. In some embodiments, a catalyst is used to aid in depolymerizing the material. In certain embodiments, the catalyst is contained in a permeable container. The depolymerized molten material can then be cooled via a heat exchanger. In some embodiments, multiple reactors are used. In certain embodiments, these reactors are connected in series. In some embodiments, the reactor(s) contain removable static mixer(s) and/or removable annular inserts.

Provided is a reactor capable of generating a proposed target solution in a short time by reacting the raw material solutions with each other while allowing a mixed raw material solution containing a plurality of kinds of raw material solutions mixed with each other to flow, and restraining the temperature of the mixed raw material solution from excessively rising. The reactor includes a reaction channel allowing the mixed raw material solution to flow and a solvent channel allowing a solvent dissolvable in the mixed raw material solution to flow. The solvent channel is connected to the reaction channel between the upstream end and the downstream end of the reaction channel so that the solvent flowing in the solvent channel is mixed with the mixed raw material solution flowing in the reaction channel from the middle of the reaction channel.

There are provided a method of producing a carbonyl compound by a flow type reaction, including introducing a triphosgene solution, a tertiary amine solution, and an active hydrogen-containing compound solution into flow channels different from each other to cause the respective solutions to flow inside the respective flow channels, joining the respective solutions that flow inside the respective flow channels simultaneously or sequentially so that a reaction between phosgene and an active hydrogen-containing compound occurs, and obtaining a carbonyl compound in a joining solution, in which a non-aqueous organic solvent is used as a solvent of each of the respective solutions and a compound having a cyclic structure is used as the tertiary amine; and a flow type reaction system that is suitable for carrying out this production method.

A process for making mesophase and/or isotropic pitch. An aromatic rich liquid is charged at high temperature and pressure to a first thermal polymerization reactor to produce an effluent stream which is flashed to remove unconverted or partially converted feed as a vapor yielding a liquid phase enriched in isotropic pitch. The enriched isotropic pitch liquid is charged to a second thermal reactor and reactor effluent flashed to produce mesophase pitch and a vapor phase. The vapor phases from both flashing steps are condensed and combined for recycle of a liquid aromatic rich stream to the first reactor. Flashing from the first reactor cools the liquid phase which is enriched in isotropic pitch. This enriched stream is mixed with a superheated fluid, preferably steam, upstream of the second reactor.

An alkylation reaction apparatus has n reactors. In the n reactors, there are m reactors including the first reactor that have three reaction zones as defined below. According to the flow direction order of alkylation reaction streams, the three reaction zones are an x reaction zone, a y reaction zone and a z reaction zone respectively; based on the mixing intensity, the mixing intensity of the y reaction zone>the mixing intensity of the x reaction zone>the mixing intensity of the z reaction zone, wherein n≥1 and n≥m. An alkylation reaction system includes the aforementioned alkylation reaction apparatus, and a liquid acid catalyzed alkylation reaction process by using the aforementioned alkylation reaction apparatus or the aforementioned alkylation reaction system.

A peptide synthesis instrument can be used for small scale peptide synthesis. The instrument can include several unique features, including a compression style reaction vessel permitting quick setup of the reaction vessel, a double reaction vessel system permitting efficient mixing without loss of solvent or solvent-to-resin contact, gravity-fed heated reservoirs establishing a fixed volume for delivery to the reaction vessel, fume-free solvent addition permitting solvent addition to fixed bottles, and an improved amino acid manifold assembly which reduces the number of components and increases the ease of use of the instrument. Each of these features improve upon the current state of the art in solid phase automated peptide synthesizers.

The present invention is directed to a process for continuous production of copper (I) nitrotetrazolate (DBX-1) by reacting aqueous copper salt with aqueous 5-nitrotetrazolate salt in the presence of a reducing agent. All the reactants are introduced into a continuous flow reactor system, which is composed of a temperature controlled tubular reactor and a mixer that allows for radial mixing. An optional stirred tank reactor may also be incorporated into the process to complete the reaction and allow for crystal growth.

A method to convert asphaltenes to partially oxidized asphaltenes comprising the steps of treating the reactor feed in a tubular reactor to produce a reactor effluent, introducing the reactor effluent to a disengagement zone of a vessel reactor, introducing an oxidizing agent stream to the asphaltene collection zone of the vessel reactor, reacting the asphaltenes in the asphaltene-rich fraction with oxygen from the oxidizing agent, withdrawing a bottom reactor effluent from the asphaltene collection zone, reducing a temperature of the bottom reactor effluent to produce a cooled bottom effluent, reducing a pressure of the cooled bottom effluent in a pressure regulator unit to produce a centrifuge feed, separating the centrifuge feed in a centrifuge to produce a centrate, mixing the centrate and the upper upgraded stream in a product mixer to produce a mixed upgraded stream, and separating the mixed upgraded stream in a three-phase separator.

A reactor and process for the production of bio-diesel. The reactor includes one or more coiled reaction lines. The lines are positioned within a tank containing a heat transfer media such as molten salt, maintained at about 750° F. A pump circulates the media within the tank. An emulsion of alcohol; refined feed stock, including glycerides and/or fatty acids; and preferably water is pumped through the reaction lines at temperatures and pressures sufficient to maintain the alcohol in a super-critical state. The curvature of the coils, pump pulsing, and the flow rate of the emulsion keep the emulsion in a turbulent state while in the reactor, ensuring thorough mixing of the alcohol and feed stock. The alcohol reacts with the glycerides and fatty acids to form bio-diesel. The reaction is fast, efficient with regard to energy input and waste generation, and requires minimal alcohol.

The present invention relates to a method for continuously preparing an ester-based composition, the method increasing a preparation yield by optimizing pressure of a reactor as a process variable of each reactor of a reaction unit in which a plurality of reactors are connected in series.