A chemical-looping system utilizes oxygen-carrier particles to produce syngas from carbonaceous fuels. The system provides a circuitous flow path for the oxygen-carrier particles, which are used to partially oxidize the fuel to produce syngas. The circuitous flow path can proceed through a plurality of unit operations, including a reducer, a conversion reactor, an oxidizer, and a combustor. The conversion reactor is designed to partially oxidize carbonaceous fuel in co-current flow with the oxygen-carrier particles to produce syngas. In embodiments including an oxidizer, the oxidizer is designed to at partially re-oxidize the carrier particles, yielding hydrogen that can be mixed with partially oxidized products from the conversion reactor to adjust syngas quality. The combustor can be used to fully oxidize the carrier particles traveling in a closed loop. Reactions carried out in the combustor are highly exothermic and yield thermal energy that is absorbed by the carrier particles. The absorbed energy is used at other parts of the process, including the conversion reactor, to drive endothermic reactions. In this manner the system can be operated autothermally or nearly so. Methods of producing syngas are also disclosed.

The invention relates to CeO.sub.2 and La.sub.2O.sub.3 for catalyzing Fe.sub.2O.sub.3Al.sub.2O.sub.3 based chemical-looping reforming of CH.sub.4 with CO.sub.2 (CL-DRM). The reaction performance of all the composite oxygen carriers was evaluated in a fixed-bed reactor at atmospheric pressure condition. The influencing factors, including temperature and time-on-stream (TOS) were investigated. The characteristics of the oxygen carriers were checked with Brunauer-Emmett-Teller (BET) analysis and X-ray diffraction (XRD). The reducibility of the composite materials was elucidated with temperature-programmed reduction by CH.sub.4 (CH.sub.4-TPR). Preliminary experimental observations suggest that the simultaneous presence of CeO.sub.2 and La.sub.2O.sub.3 can not only enhance the reactivity of Fe.sub.2O.sub.3Al.sub.2O.sub.3 toward CH.sub.4 oxidation and its oxygen releasing rate for fast reaction kinetics, but also improve the reactivity of its reduced form toward CO.sub.2 splitting.

The present invention relates to a device for producing compressed hydrogen, comprising a pressure-resistant reactor (1) with a reactor chamber having a metal-containing contact mass (2), wherein the reactor (1) comprises at least one feed line (3) for feeding fluids into the reactor chamber and at least one discharge line (4) for discharging fluids from the reactor chamber, wherein the at least one discharge line is provided with a device (5a, 5b, 5c, 5d) for controlling or regulating the flow rate, preferably having a valve, for adjusting the pressure within the reactor chamber, wherein a conveyance means is provided on at least one feed line for introducing a water-containing medium into the reactor chamber and wherein at least one discharge line (4) protrudes into the reactor chamber or opens directly into the reactor chamber, through which the compressed hydrogen is discharged from the reactor chamber, wherein the reactor chamber exhibits at least two areas that are separate from each other and connected in a gas-conducting manner, of which at least one area comprises the metal-containing contacting mass (2) and at least one additional area comprises at least one inert material (7, 13).

The invention relates to CeO.sub.2 and La.sub.2O.sub.3 for catalyzing Fe.sub.2O.sub.3Al.sub.2O.sub.3 based chemical-looping reforming of CH.sub.4 with CO.sub.2 (CL-DRM). The reaction performance of all the composite oxygen carriers was evaluated in a fixed-bed reactor at atmospheric pressure condition. The influencing factors, including temperature and time-on-stream (TOS) were investigated. The characteristics of the oxygen carriers were checked with Brunauer-Emmett-Teller (BET) analysis and X-ray diffraction (XRD). The reducibility of the composite materials was elucidated with temperature-programmed reduction by CH.sub.4 (CH.sub.4-TPR). Preliminary experimental observations suggest that the simultaneous presence of CeO.sub.2 and La.sub.2O.sub.3 can not only enhance the reactivity of Fe.sub.2O.sub.3Al.sub.2O.sub.3 toward CH.sub.4 oxidation and its oxygen releasing rate for fast reaction kinetics, but also improve the reactivity of its reduced form toward CO.sub.2 splitting.

A method of generating hydrogen in a subsurface formation, the method comprising injecting oxidizable metal particles into a subsurface formation comprising subsurface water and a geologic trap, wherein the subsurface water has a temperature of from 18 C. to 400 C. and a pressure of from 500 psi to 10,000 psi, the geologic trap comprises one or both of a structural trap or a stratigraphic trap, the geologic trap substantially prevents vertical migration of the subsurface water out of the subsurface formation, and the oxidizable metal particles react with the subsurface water to form hydrogen, metal oxides, metal hydroxides, or combinations thereof.

A hydrogen production catalyst used for generating hydrogen by splitting water, the catalyst comprising a composite metal oxide of cerium oxide and praseodymium oxide.

Provided is a hydrogen generation unit which can produce a hydrogen containing liquid more conveniently compared to a conventional hydrogen adding instrument. The hydrogen generation unit is configured such that a hydrogen generating agent which generates hydrogen by being impregnated with water, the water, and a non-flowout state maintaining unit which maintains the water in a non-flowout state where the water does not react with the hydrogen generating agent are accommodated in an accommodating body having a discharge unit for discharging a hydrogen gas, and the non-flowout state maintaining unit is configured to change the water in the non-flowout state into a flowout state where the water is reactable with the hydrogen generating agent by applying a predetermined amount of energy to the accommodating body from outside the accommodating body, whereby the water brought into the flowout state is made to react with the hydrogen generating agent by being triggered by application of the energy and hydrogen generated in the accommodating body is discharged through the discharge unit, and the hydrogen-containing liquid is produced without permeation of the liquid into the hydrogen generation unit.

A chemical-looping system utilizes oxygen-carrier particles to produce syngas from carbonaceous fuels. The system provides a circuitous flow path for the oxygen-carrier particles, which are used to partially oxidize the fuel to produce syngas. The circuitous flow path can proceed through a plurality of unit operations, including a reducer, a conversion reactor, an oxidizer, and a combustor. The conversion reactor is designed to partially oxidize carbonaceous fuel in co-current flow with the oxygen-carrier particles to produce syngas. In embodiments including an oxidizer, the oxidizer is designed to at partially re-oxidize the carrier particles, yielding hydrogen that can be mixed with partially oxidized products from the conversion reactor to adjust syngas quality. The combustor can be used to fully oxidize the carrier particles traveling in a closed loop. Reactions carried out in the combustor are highly exothermic and yield thermal energy that is absorbed by the carrier particles. The absorbed energy is used at other parts of the process, including the conversion reactor, to drive endothermic reactions. In this manner the system can be operated autothermally or nearly so. Methods of producing syngas are also disclosed.

This disclosure relates to methods for reducing CO.sub.2 emissions from a fluid catalytic cracking process by providing a chemical looping system comprising a regenerator and reducer reactor, an oxidizer reactor, and a combustor reactor, and by sequestering the carbon dioxide of a CO.sub.2 and H.sub.2O stream. Also, this disclosure relates to methods for reducing CO.sub.2 emissions from a fluid catalytic cracking process by partially oxidizing catalyst coke particles in a fluid catalytic cracking regenerator reactor to produce synthesis gas, and by providing a chemical looping system comprising a reducer reactor, an oxidizer reactor, and a combustor reactor.

Described herein are methods of using silicate materials, including silicate materials obtained from nature, synthesized, and/or obtained from industrial waste streams, to capture and store carbon dioxide. In some embodiments, the methods can also be used to form silica (e.g., high purity silica). In some embodiments, the methods can also be used to produce hydrogen.