The invention relates to a method of producing a binder comprising the steps of preparing (20) a residual material comprising amorphous alumina-rich and/or aluminium hydroxide-rich constituents, heating (30) the residual material to produce a fired material, the heating (30) of the residual material being at a temperature of >800° C.

The invention relates to the use of a hydraulic binder containing calcium aluminate, obtainable by a method in which a) prepared amorphous residual material rich in aluminium oxide and/or aluminium hydroxide is heated after the addition of a b) calcium ion-containing binder component and c) water, for the production of a constructing material.

A method for processing water treatment residuals, or other amorphous aluminium oxide or aluminium hydroxide rich waste residuals, for use in the manufacture of hydraulic binders, comprising heating the residuals to remove water and oxidise organic material contained therein, comprising controlling the temperature of the residuals during heating such that they are heated to a temperature no higher than 800° C., more preferably no higher than 650° C., to ensure that aluminium compounds in the WTR, in particular aluminium oxide and aluminium hydroxide, remain in an amorphous state. The method may comprise controlling the temperature of the water treatment residuals such that they are heated to a temperature between 350° C. and 650° C., more preferably between 400° C. and 500° C.

A material conversion apparatus includes: (a) a housing, (b) a chamber for treating the material disposed within the housing, (c) an induction coil surrounding the chamber and (d) means for exhausting or evacuating the treated content of the chamber.

The present disclosure concerns a pyrolysis residue-discharge system fluid-tightly connectable to a pyrolysis reactor delimiting a fuel-containing cavity and having a discharge opening extending therethrough, the pyrolysis residue-discharge system comprising a residue discharge duct defining a residue discharge passageway having an inlet port and an outlet port; and a reactor-connecting end portion having a through opening, the reactor-connecting end portion being fluid-tightly connectable to the pyrolysis reactor to fluidly connect the through opening of the reactor-connecting end portion with the discharge opening of the pyrolysis reactor, the reactor-connecting end portion being fluid-tightly connectable to the residue discharge duct at the inlet port thereof to provide a fluid communication between the fuel-containing cavity of the pyrolysis reactor and the residue discharge passageway via the discharge opening. It also concerns a corresponding pyrolysis reactor assembly and a pyrolysis residue discharge method.

Improved processes and systems are disclosed for producing renewable hydrogen suitable for reducing metal ores, as well as for producing activated carbon. Some variations provide a process comprising: pyrolyzing biomass to generate a biogenic reagent comprising carbon and a pyrolysis off-gas; converting the pyrolysis off-gas to additional reducing gas and/or heat; reacting at least some of the biogenic reagent with a reactant to generate a reducing gas; and chemically reducing a metal oxide in the presence of the reducing gas. Some variations provide a process for producing renewable hydrogen by biomass pyrolysis to generate a biogenic reagent, conversion of the biogenic reagent to a reducing gas, and separation and recovery of hydrogen from the reducing gas. A reducing-gas composition for reducing a metal oxide is provided, comprising renewable hydrogen according to a hydrogen-isotope analysis. Reacted biogenic reagent may also be recovered as an activated carbon product. Many variations are disclosed.

Improved processes and systems are disclosed for producing renewable hydrogen suitable for reducing metal ores, as well as for producing activated carbon. Some variations provide a process comprising: pyrolyzing biomass to generate a biogenic reagent comprising carbon and a pyrolysis off-gas; converting the pyrolysis off-gas to additional reducing gas and/or heat; reacting at least some of the biogenic reagent with a reactant to generate a reducing gas; and chemically reducing a metal oxide in the presence of the reducing gas. Some variations provide a process for producing renewable hydrogen by biomass pyrolysis to generate a biogenic reagent, conversion of the biogenic reagent to a reducing gas, and separation and recovery of hydrogen from the reducing gas. A reducing-gas composition for reducing a metal oxide is provided, comprising renewable hydrogen according to a hydrogen-isotope analysis. Reacted biogenic reagent may also be recovered as an activated carbon product. Many variations are disclosed.

Improved processes and systems are disclosed for producing renewable hydrogen suitable for reducing metal ores, as well as for producing activated carbon. Some variations provide a process comprising: pyrolyzing biomass to generate a biogenic reagent comprising carbon and a pyrolysis off-gas; converting the pyrolysis off-gas to additional reducing gas and/or heat; reacting at least some of the biogenic reagent with a reactant to generate a reducing gas; and chemically reducing a metal oxide in the presence of the reducing gas. Some variations provide a process for producing renewable hydrogen by biomass pyrolysis to generate a biogenic reagent, conversion of the biogenic reagent to a reducing gas, and separation and recovery of hydrogen from the reducing gas. A reducing-gas composition for reducing a metal oxide is provided, comprising renewable hydrogen according to a hydrogen-isotope analysis. Reacted biogenic reagent may also be recovered as an activated carbon product. Many variations are disclosed.

Improved processes and systems are disclosed for producing renewable hydrogen suitable for reducing metal ores, as well as for producing activated carbon. Some variations provide a process comprising: pyrolyzing biomass to generate a biogenic reagent comprising carbon and a pyrolysis off-gas; converting the pyrolysis off-gas to additional reducing gas and/or heat; reacting at least some of the biogenic reagent with a reactant to generate a reducing gas; and chemically reducing a metal oxide in the presence of the reducing gas. Some variations provide a process for producing renewable hydrogen by biomass pyrolysis to generate a biogenic reagent, conversion of the biogenic reagent to a reducing gas, and separation and recovery of hydrogen from the reducing gas. A reducing-gas composition for reducing a metal oxide is provided, comprising renewable hydrogen according to a hydrogen-isotope analysis. Reacted biogenic reagent may also be recovered as an activated carbon product. Many variations are disclosed.

An environmentally friendly combustion chamber for stable combustion of biomass gasification combustible gas. The combustion chamber is divided into a first stage cavity body (45) and a second stage cavity body (48) by a honeycomb-shaped heat storage body (46). A combustion pipe (41) is connected to a biomass gas inlet and a primary air distribution pipe (54), the combustion pipe (41) is connected to the first stage cavity body (45), and an ignition gun (42) and a thermocouple T1 are arranged on the first stage cavity body (45). A secondary air distribution pipe (47), opposite the honeycomb-shaped heat storage body (46), and a thermocouple T2 are arranged within the second stage cavity body (48), and the second stage cavity body (48) is connected to an outlet high temperature flue gas pipe (51). The primary air distribution pipe (54), a primary air volume adjustment valve (52), the secondary air distribution pipe (47) and a secondary air volume adjustment valve (53) are connected together to an air supply fan (49), and a controller (50) is connected to the thermocouple T1, the thermocouple T2, the primary air volume adjustment valve (52), the secondary air volume adjustment valve (53) and the air supply fan (49). The combustion chamber solves the problems of unstable combustion flames in traditional combustors, and high nitrogen oxide amounts in tail flue gas.