Disclosed are a method and system for propylene polymerization utilizing a loop slurry reactor. The method can include polymerizing propylene in a loop slurry reactor under bulk polymerization conditions to produce polypropylene. The propylene polymerization system can include i) a loop slurry reactor and a heat exchange system that is configured to cool the legs of the loop slurry reactor and/or ii) an inlet manifold that is configured to connect flashline heaters to a separator.

A system is provided that enables a continuous process that involves the introduction of particles into a reactor drum having a low oxygen environment. Heavy hydrocarbons are boiled off of the particles during the heating of the particles. The boiled off heavy hydrocarbons mix with a heated gas stream that heats the particles within the reactor drum. The heated gas stream (with the boiled off heavy hydrocarbons) exit the drum and are recirculated back to a heat source for reheating the gas stream prior to reentering the reactor drum. Repeated exposure to the elevated temperatures within the reactor drum cracks the heavy hydrocarbons into lighter hydrocarbons. The lighter hydrocarbons may then be separated out of the heated gas stream and collected for sale or use.

Improved methods of synthesizing ammonia from hydrogen sulfide and lithium nitrate are disclosed. Specifically, in a continuous cycle, hydrogen sulfide reactant is regenerated from the elemental sulfur that is extracted from a product of the ammonia synthesis, and the regenerated hydrogen sulfide is fed back into the ammonia synthesis reaction. The cycle that regenerates the hydrogen sulfide uses either a water-containing or a water and carbon-containing feedstock to facilitate the regeneration of the hydrogen sulfide from the elemental sulfur.

The present disclosure relates to processes for production of polyolefins from olefin monomer(s) in a gas phase reactor using condensing agent(s) (CAs), and in particular relates to controlling condensed phase cooling in a gas phase reactor used to polymerize olefin monomer(s). The method may include introducing first and second condensing agent(s) into the reactor at ratio(s) determined by ascertaining a stick limit for the first condensing agent, calculating an equivalence factor relating the first and second condensing agents, ascertaining total allowable condensing agent, and calculating amount of the first condensing agent removed and replaced by the second condensing agent. The method may further include calculating the dew point limit of a gas phase composition including olefin monomer(s) as well as the first and second condensing agents; and determining if introducing a mixture comprising the olefin monomer(s) and the condensing agent composition would exceed the calculated dew point limit.

A methanol synthesis plant comprising: a feed pretreating section operable to pretreat a feed stream; a synthesis gas (syngas) generation section comprising one or more reactors operable to produce a syngas synthesis product stream comprising synthesis gas from the feed stream; a methanol synthesis section comprising one or more methanol synthesis reactors operable to produce a synthesis product comprising methanol; and/or a methanol purification section operable to remove at least one component from the synthesis product to provide a purified methanol product; wherein the methanol synthesis plant is configured such that, relative to a conventional methanol synthesis plant, more of the net energy required by the methanol synthesis plant, the feed pretreating section, the syngas generation section, the methanol synthesis section, the methanol purification section, or a combination thereof, is provided by a non-carbon based energy source, a renewable energy source, and/or electricity.

An apparatus for producing methanol from carbon dioxide. The apparatus includes a first circulation process for a circulating water and methanol which includes an absorption stage for carbon dioxide, a desorption stage with a hydrogen feed, a first heat exchanger, an outlet, a circulation pump, and an expansion throttle. The second circulation process for methanol, water, carbon dioxide and hydrogen includes the desorption stage, a first liquid-gas phase separation stage with a return conduit for liquid phases to the desorption stage, and a gas outlet from and an inlet into the desorption stage. The third circulation process for carbon dioxide and hydrogen includes a methanol synthesis reactor, a gas outlet of the first liquid-gas phase separation stage which opens out into the third circular conduit and an inlet into which the third circular conduit opens, a second heat exchanger, a gas outlet in the third circular conduit, and a fan.

A process for performing a continuous gas/liquid biphasic high-pressure reaction, wherein a gas and a liquid are introduced into a backmixed zone of a reactor and in the backmixed zone the gas is dispersed in the liquid by stirring, injection of gas and/or a liquid jet, a reaction mixture consecutively traverses the backmixed zone and a zone of limited backmixing, and a liquid reaction product is withdrawn at a reaction product outlet of the zone of limited backmixing, wherein the reactor comprises: an interior formed by a cylindrical vertically oriented elongate shell, a bottom and a cap, wherein the interior is divided by means of internals into the backmixed zone, the zone of limited backmixing and a cavity, a first cylindrical internal element which in the interior extends in the longitudinal direction of the reactor and which delimits the zone of limited backmixing from the backmixed zone, backmixing-preventing second internal elements in the form of random packings, structured packings or liquid-permeable trays arranged in the zone of limited backmixing and a third internal element which in the interior extends in the longitudinal direction of the reactor and is open at the bottom, wherein the third internal element forms the cavity in which gas bubbles collect and do not escape upwards, thus preventing the volume of the cavity from being occupied by liquid and reducing the reaction volume. The reaction volume of the reactor used in the process can be reversibly reduced in simple fashion. The invention further relates to a process for adapting the reaction volume of a reactor suitable for performing a gas/liquid biphasic high-pressure reaction having an outlet for a liquid reaction product in which an internal element is arranged so as to form a cavity open at the bottom in which gas bubbles collect and do not escape upwards, thus preventing the volume of the cavity from being occupied by liquid and reducing the reaction volume.

A method for recovering a distillable, anhydrous methane-sulfonic acid (MSA) liquid phase from an anhydrous 2-phase gas-liquid mixture wherein the anhydrous 2-phase gas-liquid mixture is generated by sulfonating methane (CH.sub.4) with sulfur trioxide (SO.sub.3) in an MSA-forming reactor, or reactor system, according to a radical chain reaction wherein the method comprises (i) separating the gas phase from the liquid phase, (ii) passing the separated liquid phase into a stripping column, and (iii) recovering the stripped anhydrous liquid phase.

A sulfuric acid generating system can include: a primary burn chamber; an exhaust pipe extending from the burn chamber at a first end to an opposite second end; a secondary burn chamber located between the first end and second end; and a primary venturi pump having a gas inlet coupled to an outlet at the second end of the exhaust pipe and having an aqueous media in let and having a fluid outlet. A method of producing sulfurous acid can include: providing sulfur to the primary burn chamber; burning a first portion of the sulfur in the primary burn chamber to form a first portion of sulfur dioxide; burning a second portion of the sulfur in the secondary burn chamber to form a second portion of sulfur dioxide; and mixing the first portion and second portion of sulfur dioxide with an aqueous composition so as to produce aqueous sulfurous acid.

A system and method for processing a treated feed slurry produced by a slurry reactor. The method and system include mixing a chemical separation feed with the treated feed slurry produced by the slurry reactor to chemically separate solid catalyst particles in the treated feed slurry by dissolving the solid catalyst particles using an acid or base in the chemical separation feed. A heavy oil upgrading process that includes the system and method is also described.