A photochemical reactor is disclosed which includes a reaction chamber, the reaction chamber includes a frame, one or more circuit boards each coupled to the frame and each carrying a plurality of light sources, a power source coupling, adapted to power the one or more circuit boards, and a vial receiver centrally disposed about the one or more circuit boards. The photochemical reactor further includes an agitator configured to rotate the vial receiver.

The present disclosure is directed to systems and methods for reforming methane into hydrogen and a hydrocarbon fuel. In example embodiments, the methane reformer integrates a photocatalytic steam methane reforming (P-SMR) system with a subsequent photocatalytic dry methane reforming (P-DMR) system.

The solar-powered oxygen production system for hospitals is useful for producing oxygen in hospital settings without the need for an external power source. The system includes one or more photovoltaic (PV) solar panels mounted on the roof of a hospital and an oxygen production system housed within the equipment room of the hospital. The solar panels provide the electrical power needed for the oxygen production system. The solar panels are mounted on the roof using solar panel supports. The number of panels and the power output of each panel can be selected depending on the electrical power requirements of the oxygen production system. The oxygen production system includes an LED for activating a black phosphorous catalyst in the atmospheric air to convert water vapor in the air into hydrogen and oxygen.

The present invention provides a photolytic converter for converting reactant molecules in a fluid sample into product molecules by photolytic dissociation with electromagnetic radiation. The converter has a reaction chamber in communication with one or more electromagnetic radiation sources, an inflow conduit for conveying the fluid sample into the reaction chamber, and an outflow conduit for conveying the fluid sample out of the reaction chamber into a receptacle, wherein at least one of the first and outflow conduits extends into the reaction chamber. The receptacle can comprise detection means for generating a signal indicative of a concentration of product molecules in the processed fluid sample.

A gas processing system includes an input gas supply, an output gas storage container and/or an inlet to a secondary reactor, and a solar-thermal reactor. The solar-thermal reactor uses a solar collector to focus sunlight onto a reactor, the reactor having a housing that encloses a reaction chamber, a catalyst arranged therein, an inlet for receiving the input gas and an outlet for expelling the output gas. Sunlight is focused by the solar collector to heat the reactor and thereby chemically convert the input gas from the gas supply into the output gas that can be stored in the output gas container or directed towards the secondary reactor.

A solar-driven methanol reforming system for hydrogen production includes a water storage tank, high-temperature solar collector tubes, a thermocouple, valves, preheaters, an evaporator, a reactor, a heat exchanger, a mixed solution (methanol and water) storage tank, a gas separator, a pump, a carbon dioxide storage tank, a hydrogen storage tank, and pipes; the present invention utilizes solar energy to provide heat required for hydrogen production by methanol reforming, and stores some heat in a phase change material to supply heat for the methanol reforming reaction when sunlight is weak; the system does not need additional energy supply, thus saving energy consumption from traditional electric heating or fuel heating.

The present invention provides a method of controlling back reactions or recombination reactions of product molecules formed in a dissociation reaction of reactant molecules of a fluid sample, in a reaction chamber. The method comprises introducing the fluid sample into the reaction chamber through one or more inlets, initiating the dissociation reaction of the reactant molecules of the fluid sample in the reaction chamber to form the product molecules, creating a patterned flow of the fluid sample in the reaction chamber to reduce/minimize disordered and/or turbulent mixing of the reactant molecules and/or product molecules in the fluid sample, and conveying the fluid sample comprising the product molecules out from the reaction chamber through one or more outlets.

A solar thermochemical processing system is disclosed. The system includes a first unit operation for receiving concentrated solar energy. Heat from the solar energy is used to drive the first unit operation. The first unit operation also receives a first set of reactants and produces a first set of products. A second unit operation receives the first set of products from the first unit operation and produces a second set of products. A third unit operation receives heat from the second unit operation to produce a portion of the first set of reactants.

Included herein are methods for photodriven hydrogenation of N.sub.2, the methods comprising, for example: hydrogenating N.sub.2 to NH.sub.3 in the presence of a light, an organic transfer agent, and a first metal-containing catalyst; wherein: the transfer agent and the first catalyst are in a solution; the transfer agent comprises n chemically transferable electrons and protons, n being an integer equal to or greater than 1; the step of hydrogenating comprises at least one charge-transfer reaction via which the transfer agent donates at least one electron and at least one proton to one or more other chemical species; the step of hydrogenating comprises at least one photochemical reaction; and the light is characterized by energy sufficient to drive the at least one photochemical reaction. Also disclosed herein are methods comprising regenerating a spent-transfer agent back into the transfer agent.

The inventive concepts disclosed relate to the production of green and blue hydrogen from hydrocarbons using visible light (from a laser, lamp or sun) and defect-engineered boron-rich photocatalysts. We demonstrate that the environment of the B atoms in the lattice can be tuned to favor the dehydrogenation of desired hydrocarbons on reaction sites under visible light. In addition to the hydrogen produced in gas form, carbon atoms are captured by the catalyst and form structures of potential higher value for future applications. Further study of the dark carbonaceous product revealed a graphitic aspect of the material. These findings highlight a new functionality of 2D materials for visible light-assisted capture and conversion of hydrocarbons, with great potential for green hydrogen production ― i.e, hydrogen produced from renewable energy and without the release of CO or CO.sub.2.