A method for treating carbonaceous material, the method includes a) providing a first carbonaceous material CM1 contaminated with micro-pollutants and/or microplastics, and providing a second carbonaceous material CM2 free of micro-pollutants or microplastics, b) subjecting the first carbonaceous material CM1 to hydrothermal gasification in a HTG reactor, thereby producing an inorganic solid residue, a first gaseous fraction G1 comprising CH.sub.4, CO, CO.sub.2 and H.sub.2 and a filtrate F1 free of micro-pollutants or microplastics optionally containing readily biodegradable carbons such as VFAs, c) subjecting the second carbonaceous material CM2 together with at least part of the filtrate F1 to an anaerobic treatment step in an anaerobic tank, leading to a digestate free of micro-pollutants or microplastics and optionally a second gaseous fraction G2 containing CH.sub.4 and CO.sub.2. An installation for treating carbonaceous material is also provided.

A method for treating carbonaceous material, the method includes a) providing a first carbonaceous material CM1 contaminated with micro-pollutants and/or microplastics, and providing a second carbonaceous material CM2 free of micro-pollutants or microplastics, b) subjecting the first carbonaceous material CM1 to hydrothermal gasification in a HTG reactor, thereby producing an inorganic solid residue, a first gaseous fraction G1 comprising CH.sub.4, CO, CO.sub.2 and H.sub.2 and a filtrate F1 free of micro-pollutants or microplastics optionally containing readily biodegradable carbons such as VFAs, c) subjecting the second carbonaceous material CM2 together with at least part of the filtrate F1 to an anaerobic treatment step in an anaerobic tank, leading to a digestate free of micro-pollutants or microplastics and optionally a second gaseous fraction G2 containing CH.sub.4 and CO.sub.2. An installation for treating carbonaceous material is also provided.

The present disclosure provides an integrated process and a Cu/Zn-based catalyst system for synthesizing methanol from CO.sub.2 and generating electricity from hydrocarbon feedstock. The process includes steps of gasifying hydrocarbon feedstock into syngas by using oxygen and using the produced syngas as a fuel in a power generation unit, reusing a first part of an exhaust stream of the power generation unit as a reactant in the gasification unit. Using a second part of the said exhaust stream as a reactant for methanol synthesis in a methanol reactor, wherein, the second part is treated to separate CO.sub.2 and water, and CO.sub.2 is used as the reactant for methanol synthesis. Operating an electrolyzer during non-peak hours to produce hydrogen, wherein, a required stoichiometric ratio of the produced hydrogen is transferred into the methanol reactor for methanol synthesis, wherein, a Cu/Zn-based catalyst system is used for methanol synthesis through a direct hydrogenation reaction of CO.sub.2.

The present disclosure provides an integrated process and a Cu/Zn-based catalyst system for synthesizing methanol from CO.sub.2 and generating electricity from hydrocarbon feedstock. The process includes steps of gasifying hydrocarbon feedstock into syngas by using oxygen and using the produced syngas as a fuel in a power generation unit, reusing a first part of an exhaust stream of the power generation unit as a reactant in the gasification unit. Using a second part of the said exhaust stream as a reactant for methanol synthesis in a methanol reactor, wherein, the second part is treated to separate CO.sub.2 and water, and CO.sub.2 is used as the reactant for methanol synthesis. Operating an electrolyzer during non-peak hours to produce hydrogen, wherein, a required stoichiometric ratio of the produced hydrogen is transferred into the methanol reactor for methanol synthesis, wherein, a Cu/Zn-based catalyst system is used for methanol synthesis through a direct hydrogenation reaction of CO.sub.2.

The present disclosure relates to a process plant and a process for production of a hydrogen rich gas, comprising the steps of (a) directing an amount of a synthesis gas comprising at least 15%, 50% or 80% on dry basis of CO and H.sub.2 in combination, a gas comprising steam, and a recycled intermediate product gas to be combined into a first reactor feed gas, (b) directing said first reactor feed gas to contact a first material catalytically active in water gas shift reaction, producing an intermediate product gas, (c) splitting said intermediate product gas in the recycled intermediate product gas and a remaining intermediate product gas, (d) combining said remaining intermediate product gas with a further amount of synthesis gas forming a second reactor feed gas, (e) directing said second reactor feed gas to contact a second material catalytically active in the water gas shift reaction, producing a product gas, characterized in the H.sub.2O:CO ratio in said first reactor feed gas being from 0.5 to 2.0 and the H.sub.2O:CO ratio in said second reactor feed gas being from 0.5 to 2.0. with the associated benefit of distributing the heat development and thus reducing the maximum temperature in the reactors by limiting the extent of reaction of the reacting mixture, and thereby reducing the amount of steam required for limiting methanation.

The present invention deals with catalysts for the conversion of CO by the shifting reaction of high temperature water gas, free from chromium and iron, consisting of alumina promoted by potassium, by zinc and copper oxides and in a second embodiment also additionally nickel. The catalysts thus prepared maintain high CO conversion activity, not having the environmental limitations or operating limitations with low excess steam in the process, which exist for catalysts in accordance with the state of the art. Such catalysts are used in the hydrogen or synthesis gas production process by the steam reforming of hydrocarbons, allow the use of low steam/carbon ratios in the process, exhibiting high activity and stability to thermal deactivation and lower environmental restrictions for production, storage, use and disposal, than the industrially used catalysts based on iron, chromium, and copper oxides.

The present invention deals with catalysts for the conversion of CO by the shifting reaction of high temperature water gas, free from chromium and iron, consisting of alumina promoted by potassium, by zinc and copper oxides and in a second embodiment also additionally nickel. The catalysts thus prepared maintain high CO conversion activity, not having the environmental limitations or operating limitations with low excess steam in the process, which exist for catalysts in accordance with the state of the art. Such catalysts are used in the hydrogen or synthesis gas production process by the steam reforming of hydrocarbons, allow the use of low steam/carbon ratios in the process, exhibiting high activity and stability to thermal deactivation and lower environmental restrictions for production, storage, use and disposal, than the industrially used catalysts based on iron, chromium, and copper oxides.

A method produces acetic acid and includes a reaction step, a first purification step, a second purification step, and a third purification step. In the reaction step, a material mixture including methanol, carbon monoxide, a catalyst, and an iodide is subjected to a methanol carbonylation reaction in a reactor (1) to form acetic acid. In the first purification step, a crude acetic acid stream including acetic acid formed in the reaction step is subjected to distillation in a distillation column (3) to give a first acetic acid stream enriched with acetic acid. In the second purification step, the first acetic acid stream is subjected to distillation in a distillation column (5) to give a second acetic acid stream further enriched with acetic acid. In the third purification step, an acetic acid stream is subjected to purification in an additional purification unit (e.g., a distillation column (6)) while controlling the corrosive iodine concentration in the acetic acid stream passing through the unit to 100 ppm or less, to give a third acetic acid stream still further enriched with acetic acid. The method for producing acetic acid is suitable for restraining corrosion of the acetic acid production equipment.

A method produces acetic acid and includes a reaction step, a first purification step, a second purification step, and a third purification step. In the reaction step, a material mixture including methanol, carbon monoxide, a catalyst, and an iodide is subjected to a methanol carbonylation reaction in a reactor (1) to form acetic acid. In the first purification step, a crude acetic acid stream including acetic acid formed in the reaction step is subjected to distillation in a distillation column (3) to give a first acetic acid stream enriched with acetic acid. In the second purification step, the first acetic acid stream is subjected to distillation in a distillation column (5) to give a second acetic acid stream further enriched with acetic acid. In the third purification step, an acetic acid stream is subjected to purification in an additional purification unit (e.g., a distillation column (6)) while controlling the corrosive iodine concentration in the acetic acid stream passing through the unit to 100 ppm or less, to give a third acetic acid stream still further enriched with acetic acid. The method for producing acetic acid is suitable for restraining corrosion of the acetic acid production equipment.

The present invention relates to a process for converting carbon dioxide and hydrogen by performing a reverse water gas shift reaction at elevated temperature, the process comprising introducing carbon dioxide, hydrogen and oxygen into a reaction vessel having an inlet and an outlet, and, wherein the reverse water gas shift reaction takes place in two different zones of the reaction vessel, being a top zone (z1) adjacent to a bottom zone (z2). The process produces a product stream comprising mainly carbon monoxide, hydrogen and water. The process is useful in reducing the carbon footprint of certain industrial technologies, and in addition, the process is useful in the production of synthesis gas.