A metal chloride generator is provided. The metal chloride generator is a metal chloride centrifugal reactor that can be operated under conditions sufficient to cause metal particles and chlorine in the generator to be brought into contact with one another and react using centrifugal force to form metal chloride. A process for manufacturing titanium dioxide that utilizes the metal chloride generator is also provided.

Counter-flow heat exchanger is constructed with plenums at either end that separate the opposing fluids, the channels of which are arrayed in a checkerboard patterns, such that any given channel is surrounded by channels of opposing streams on four sides—laterally on both sides and vertically above and below.

Disclosed are a process and a system for treating contaminated soil. The process includes introducing a contaminated soil to an agitation unit. Ozone is supplied to the agitation unit thereby forming a soil-gas mixture, and the soil-gas mixture is agitated for sufficient time for the ozone to contact the contaminants thereby forming an ozone-treated soil and a residual gas-particulates mixture. The ozone-treated soil and the residual gas-particulates mixture are removed from the agitation unit. If necessary, remaining ozone is then flushed from the soil. The process occurs under negative pressure to prevent ozone from being released to the atmosphere.

Provided herein are methods, devices and systems for processing of carbonaceous compositions. The processing may include the manufacture (or synthesis) of oxidized forms of carbonaceous compositions and/or the manufacture (or synthesis) of reduced forms of oxidized carbonaceous compositions. Some embodiments provide methods, devices and systems for the manufacture (or synthesis) of graphite oxide from graphite and/or for the manufacture (or synthesis) of reduced graphite oxide from graphite oxide.

An alternative process and device for carrying out Fischer Tropsch (FT) syntheses is proposed, allowing the reactant entities that take part in the FT reaction to be activated and their contributions, whether by quantity or by proportion, to be adjusted. The process consists in making a particulate phase, optionally consisting of catalytic particles, flow through a reactor. While flowing through the reactor, the particulate phase is subjected at regular intervals to the action of a plasma obtained from a gas, such as hydrogen, thus enabling hydrogen activation for hydrogenation of carbon monoxide, or carbon monoxide activation in order to lengthen the carbon chains.

An alternative process and device for carrying out Fischer Tropsch (FT) syntheses is proposed, allowing the reactant entities that take part in the FT reaction to be activated and their contributions, whether by quantity or by proportion, to be adjusted. The process consists in making a particulate phase, optionally consisting of catalytic particles, flow through a reactor. While flowing through the reactor, the particulate phase is subjected at regular intervals to the action of a plasma obtained from a gas, such as hydrogen, thus enabling hydrogen activation for hydrogenation of carbon monoxide, or carbon monoxide activation in order to lengthen the carbon chains.

Supported chromium catalysts with an average valence less than +6 and having a hydrocarbon-containing or halogenated hydrocarbon-containing ligand attached to at least one bonding site on the chromium are disclosed, as well as ethylene-based polymers with terminal alkane, aromatic, or halogenated hydrocarbon chain ends. Another ethylene polymer characterized by at least 2 wt. % of the polymer having a molecular weight greater than 1,000,000 g/mol and at least 1.5 wt. % of the polymer having a molecular weight less than 1000 g/mol is provided, as well as an ethylene homopolymer with at least 3.5 methyl short chain branches and less than 0.6 butyl short chain branches per 1000 total carbon atoms.

The invention relates to a process for producing energy products, notably fuel, by catalytic cracking of a hydrocarbon-based solid material without coke formation, in which a cracking dispersion (40) is heated, said dispersion comprising: a solid material (1) in divided form containing at least one hydrocarbon-based compound; a liquid (30) which is inert with respect to catalytic cracking;
so that the cracking dispersion (40) reaches a temperature suitable for allowing catalytic cracking of at least one hydrocarbon-based compound;
characterized in that the cracking temperature is reached by mixing an amount of cracking dispersion (40) and an amount of inert liquid (30) brought to a temperature above the cracking temperature, such that the mixture formed reaches a temperature above the cracking temperature and below the temperature for formation of coke, dioxin and furan. The invention also relates to a device for performing such a process.

A system for hydrocarbon decomposition comprising a reactor volume, a mechanism to distribute the liquid catalyst as a liquid mist, a distributor to distribute a hydrocarbon reactant, a heat source, a separator to separate the solid product from the liquid catalyst, a re-circulation path and mechanism to re-circulate the liquid catalyst, and an outlet for at least one gaseous product. A system to distribute a liquid to an enclosed volume as a mist has a plurality of orifices designed to break the liquid into a mist. A method to decompose a hydrocarbon reactant includes generating a mist of a liquid catalyst, heating the reactor volume, introducing a hydrocarbon reactant into the reactor volume to produce a solid product and a gaseous product, separating the solid product from the liquid catalyst, removing the solid and gaseous products from the reactor volume, and recirculating the liquid catalyst to the reactor volume.

The present disclosure relates to a shell-and-multi-triple concentric-tube reactor and a shell-and-multi-triple concentric-tube heat exchanger, and to a shell-and-multi-triple concentric-tube reactor and a shell-and-multi-triple concentric-tube heat exchanger which provide a new type of reactor and heat exchanger, thereby maximizing catalyst performance and improving performance of the reactor by optimizing heat exchange efficiency and a heat flow, uniformly distributing a reactant, and increasing a flow rate of the reactant, and accordingly making the reactor and the heat exchanger compact.