A method for forming catalytically treated pyrolytic vapor product from pyrolyzable material, the method comprising burning fuel in a fluidized bed boiler, thereby heating some particulate material; transferring at least some of the heated particulate material or some other heated particulate material to a pyrolysis reactor to pyrolyze some pyrolyzable material in the pyrolysis reactor; and conveying at least some pyrolytic vapor through a catalyst bed comprising catalyst material; and conveying at least part of the formed side products upstream back to the process; thereby producing the catalytically treated pyrolytic vapor product in an resource efficient manner. In addition, a system configured to produce catalytically treated pyrolytic vapor product from pyrolyzable material. The system comprises a fluidized bed boiler; a pyrolysis reactor; a catalytic reactor; means for conveying some heated particulate material to the pyrolysis reactor; a pipeline for conveying at least some pyrolytic vapor from the pyrolysis reactor into the catalytic reactor and means for conveying at least part of the formed side products upstream back to the process for recovering heat and chemical energy bound to the side products.

A separator system for treating a gas from a biomass gasification system, including: first and second cyclones, where the first cyclone includes an inlet for receiving a gas from a biomass gasification unit, the first cyclone being arranged for removing particulate matter from the gas from the biomass gasification unit in order to provide a first cleaner gas, piping arranged to lead the first cleaner gas to the second cyclone, where the second cyclone is arranged to remove particulate matter from the first cleaner gas in order to provide a second cleaner gas, a pipe arranged to lead the second cleaner gas to a special piping element, the latter including a burner, thereby providing a third cleaned gas, and a gas distribution unit arranged to lead the third cleaned gas to one or more tar reformer units. Also, a method of treating a gas from a biomass gasification system.

A method for recovering fibers embedded in a composite material including loading a furnace chamber with a volume of the composite material; thermolyzing the composite material in the furnace chamber, resulting in a gaseous fraction that is continuously evacuated from the furnace chamber, and a residue of fibers covered with char that is left in the furnace chamber; cracking the gaseous fraction from the thermolyzing operation, resulting in a mixture of condensable and non-condensable gases that can be recycled; injecting a stream of an oxygen-containing gas into the still hot furnace chamber after the thermolyzing is completed therein, to burn the char from the fibers in an exothermic combustion.

A synthesis gas production process from CO.sub.2 and H.sub.2O with a co-electrolysis, wherein the CO.sub.2 and CH.sub.4 content of the produced gas is reduced on the cathode side.

A chemical reaction system comprises: a supply source to generate a first carbon compound including at least one of carbon monoxide and carbon dioxide; an electrochemical reaction device to generate a second carbon compound including carbon monoxide by a reduction reaction of carbon dioxide; a reactor to generate a product including a third carbon compound by a chemical reaction of a reactant including hydrogen and at least one of the first and second carbon compounds; and a flow path through which the second carbon compound is supplied from the electrochemical reaction device to at least one of the supply source and the reactor.

Efficiency of a thermochemical regeneration combustion system is enhanced by incorporation of gaseous products from pyrolysis of fuel such as biomass.

Efficiency of a thermochemical regeneration combustion system is enhanced by incorporation of gaseous products from pyrolysis of fuel such as biomass.

A continuous multi-stage vertically sequenced gasification process for conversion of solid carbonaceous fuel material into clean (low tar) syngas. The process involves forming a pyrolysis residue bed having a uniform depth and width to pass raw syngas there through for an endothermic reaction, while controlling the reduction zone pressure drop, resident time and syngas flow space velocity during the endothermic reaction to form substantially tar free syngas, to reduce carbon content in the pyrolysis residue, and to reduce the temperature of raw syngas as compared to the temperature of the partial oxidation zone.

A family of highly charged crystalline microporous metallophosphate molecular sieves designated PST-19 has been synthesized. These high charge density metallophosphates are represented by the empirical formula of:
R.sup.p+.sub.rA.sup.+.sub.mM.sup.2+.sub.xE.sub.yPO.sub.z
where A is an alkali metal such as potassium, R is an organoammonium cation such as tetraethylammonium, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. The molecular sieves of the invention as synthesized exhibit an x-ray diffraction pattern as shown in Table A and are modified by a process selected from calcination, ammonia calcination or ion-exchange. The PST-19 family of materials are among the first MeAPO-type molecular sieves to be stabilized by combinations of alkali and quaternary ammonium cations, enabling unique compositions. The PST-19 family of molecular sieves has the SBS topology and catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

A family of highly charged crystalline microporous metallophosphate molecular sieves designated PST-19 has been synthesized. These high charge density metallophosphates are represented by the empirical formula of:
R.sup.p+.sub.rA.sup.+.sub.mM.sup.2+.sub.xE.sub.yPO.sub.z
where A is an alkali metal such as potassium, R is an organoammonium cation such as tetraethylammonium, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. The molecular sieves of the invention as synthesized exhibit an x-ray diffraction pattern as shown in Table A and are modified by a process selected from calcination, ammonia calcination or ion-exchange. The PST-19 family of materials are among the first MeAPO-type molecular sieves to be stabilized by combinations of alkali and quaternary ammonium cations, enabling unique compositions. The PST-19 family of molecular sieves has the SBS topology and catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.