Embodiments of the invention improve the performance, safety, and efficiency of the gasification process. Embodiments of the invention improve downdraft gasification by improving upon the systems and methods for fuel preparation and by addressing gasifier bridging and channeling. Unique parts of the system include a unique hearth and grate design, a programmable logic controller and interface for managing the gasification process, an improved filtration system, a unique system for eliminating mist, a unique system for cooling gas, a unique combined flare, an integrated auger system, and a new system and method for sampling gas.

The present invention relates to a method of controlling prepurifier cycle time by monitoring ambient CO.sub.2 level in order to prevent CO.sub.2 breakthrough occurrences caused by extreme instantaneous variations in ambient CO.sub.2 level. Rather than operating solely by prepurifier design bed capacity, the method of the invention continuously updates bed capacity for the contaminants using the feed temperature, pressure and contaminants composition, calculating the total amount of contaminants that were fed to the prepurifier during the feed step and estimates the perturbation front velocity, i.e., the velocity at which the contaminants front coming from an extreme instantaneous variations of ambient level is going to propagate inside the adsorbents bed. Estimating the perturbation front velocity allows for a more precise estimate of the maximum time remaining for the feed step before starting to experience CO.sub.2 breakthrough. This eliminates the need to switch the online bed unnecessarily early and risking shorter regeneration for the offline bed.

It is provided a process for increasing production of carbon monoxide (CO) and recycling carbon dioxide when treating synthesis gas using a carbon dioxide-to-carbon monoxide conversion unit, such as a Reverse Water Gas Shift (RWGS) reactor, converting excess CO.sub.2 from the produced syngas to additional CO, using an external source of green, renewable or low carbon intensity hydrogen.

It is provided a process for increasing production of carbon monoxide (CO) and recycling carbon dioxide when treating synthesis gas using a carbon dioxide-to-carbon monoxide conversion unit, such as a Reverse Water Gas Shift (RWGS) reactor, converting excess CO.sub.2 from the produced syngas to additional CO, using an external source of green, renewable or low carbon intensity hydrogen.

The present disclosure generally relates to the utilization of a fine mineral matter in the process of upgrading the liquid products obtained by thermolysis or pyrolysis of solid plastic waste or biomass or from cracking, coking or visbreaking of petroleum feedstocks. More particularly, the present disclosure is directed to a process of stabilization of the free-radical intermediates formed during thermal or catalytic cracking of hydrocarbon feedstocks including plastic waste and on a process of catalytic in-situ heavy oil upgrading. The fine mineral matter may be derived from natural sources or from synthetic sources.

A water gas shift reaction is carried out on a feed gas comprising carbon monoxide to produce carbon dioxide and hydrogen gas. The feed gas is split into multiple input streams flowed into respective reactors coupled in series. Steam is supplied to the input stream fed to the first reactor. The shift reaction is carried out in each reactor, with an overall reduced consumption of steam relative to the amount of gas shifted. The water gas shift reaction may be performed in conjunction with removing acid gas compounds from a process gas such as, for example, syngas or natural gas, by flowing a feed gas into a desulfurization unit to remove a substantial fraction of sulfur compounds from the feed gas and flowing the resulting desulfurized gas into a CO.sub.2 removal unit to remove a substantial fraction of CO.sub.2 from the desulfurized gas.

A water gas shift reaction is carried out on a feed gas comprising carbon monoxide to produce carbon dioxide and hydrogen gas. The feed gas is split into multiple input streams flowed into respective reactors coupled in series. Steam is supplied to the input stream fed to the first reactor. The shift reaction is carried out in each reactor, with an overall reduced consumption of steam relative to the amount of gas shifted. The water gas shift reaction may be performed in conjunction with removing acid gas compounds from a process gas such as, for example, syngas or natural gas, by flowing a feed gas into a desulfurization unit to remove a substantial fraction of sulfur compounds from the feed gas and flowing the resulting desulfurized gas into a CO.sub.2 removal unit to remove a substantial fraction of CO.sub.2 from the desulfurized gas.

A method for gas separation, purification and clarification by FTrPSA uses the temperature and pressure of different raw gases as well as the differences in adsorption separation coefficients and physicochemical properties among all components in the raw gases at a temperature range of 80-200 C. and a pressure range of 0.03-4.0 Mpa, regulates the adsorption or desorption regeneration operation in the PSA cycle process by coupling various separation methods, and expands the adsorption theory that the PSA or TSA separation process is limited to the cyclic operation of adsorption and desorption regeneration through pressure or temperature changes, thus realizing the gradient utilization of energy in the process of gas separation, purification and clarification as well as the easy-to-match and easy-to-balance cyclic operation of adsorption and desorption regeneration in the process of intercooling & shallow-cooling and medium & high-temperature PSA separation to separate, purify and clarify various raw gases.

A method for gas separation, purification and clarification by FTrPSA uses the temperature and pressure of different raw gases as well as the differences in adsorption separation coefficients and physicochemical properties among all components in the raw gases at a temperature range of 80-200 C. and a pressure range of 0.03-4.0 Mpa, regulates the adsorption or desorption regeneration operation in the PSA cycle process by coupling various separation methods, and expands the adsorption theory that the PSA or TSA separation process is limited to the cyclic operation of adsorption and desorption regeneration through pressure or temperature changes, thus realizing the gradient utilization of energy in the process of gas separation, purification and clarification as well as the easy-to-match and easy-to-balance cyclic operation of adsorption and desorption regeneration in the process of intercooling & shallow-cooling and medium & high-temperature PSA separation to separate, purify and clarify various raw gases.

A process and a device for treating a flow of furnace gas with a pressure of more than 1 bar flowing through a channel. A powder agent, such as a powder comprising alkali reagents, such as lime, and/or absorbents, such as activated coal, is injected under an overpressure into the furnace gas flow via an injector which is positioned centrally within the channel The powder agent may be fluidized. The pressure for injecting the powder may be adjusted by controlling the volume of fluidization gas vented via a venting outlet.