The present disclosure belongs to the field of single-atom catalytic degradation of refractory organic pollutants, and provides a single-atom catalyst for activation of persulfate to generate pure singlet oxygen (1O2) as well as a preparation method and an application thereof. The single-atom catalyst of the present disclosure includes supports and single iron atoms loaded on the support; the supports are graphitic carbon nitride nanosheets; the single iron atoms are bound to the supports in the form of a Fe—N4 coordination structure. The present disclosure employs graphitic carbon nitride nanosheets as the supports, so that the single iron atoms have a uniform surrounding environment and the persulfate is only converted into 1O2 when being activated; 1O2 has good selectivity and anti-interference ability, so the single-atom catalyst provided in the present disclosure may have excellent selectivity and anti-interference performance in the degradation of organic pollutants.

An oxygen concentration system may comprise a pressure sensor, a movement sensor, and a controller configured to use one or more pressure signals obtained from the pressure sensor and a movement signal obtained from the movement sensor to determine when to release a bolus of oxygen enriched air. In some implementations, the controller may adjust a trigger threshold based on an initial pressure signal obtained from the pressure sensor and the movement signal obtained from the movement sensor. In some implementations, the controller may adjust a pressure signal obtained from the pressure sensor based on the movement signal obtained from the movement sensor. In some implementations, the controller may detect a potential onset of inhalation from a pressure signal obtained from the pressure sensor and determine whether to verify the potential onset of inhalation based on the movement signal obtained from the movement sensor.

The present invention generally relates to various polycyclic aromatic selenoxide compounds, methods for preparing these compounds, and methods of us these and other compounds to generate ground state atomic oxygen.

A method and system for decarbonization of a hydrocarbon conversion process such as steam methane reforming process for hydrogen production utilizing oxygen transport membrane reactors. The system employs catalyst-containing reforming reactors for converting natural gas into synthesis gas which is further treated in high temperature or medium temperature water gas shift reactors and fed to a hydrogen PSA to produce hydrogen product. The system further employs oxygen transport membrane reactors thermally coupled to reforming reactors and configured to oxy-combust about 90% to about 95% of combustibles in PSA tail gas that may be optionally mixed with natural gas. The oxy-combustion product stream leaving the oxygen transport membrane reactors contains about 90% of the carbon provided to the feed of the reforming reactor. The carbon dioxide in the oxy-combustion product stream can be recovered and further purified for utilization or geologic storage or liquefied to form a liquid carbon dioxide product.

Embodiments provide novel devices, nanowires, apparatuses, artificial leaves, photoelectrodes and membranes for photochemical energy production and methods of fabricating the same. The devices, apparatuses, artificial leaves, photoelectrodes, and membranes are planar and are embedded with nanowires, including InGaN nanowires. The unique devices, artificial leaves, apparatuses photoelectrodes, and nanowire-embedded membranes provide a high degree of flexibility and incorporate a large amount of indium, making them valuable for use for hydrogen production from sunlight and water. Embodiments also provide flexible substrates combining water oxidation and hydrogen reduction in a seamless manner to enhance the overall efficiency of water splitting.

The present disclosure belongs to the field of single-atom catalytic degradation of refractory organic pollutants, and provides a single-atom catalyst for activation of persulfate to generate pure singlet oxygen (1O2) as well as a preparation method and an application thereof. The single-atom catalyst of the present disclosure includes supports and single iron atoms loaded on the support; the supports are graphitic carbon nitride nanosheets; the single iron atoms are bound to the supports in the form of a Fe—N4 coordination structure. The present disclosure employs graphitic carbon nitride nanosheets as the supports, so that the single iron atoms have a uniform surrounding environment and the persulfate is only converted into 1O2 when being activated; 1O2 has good selectivity and anti-interference ability, so the single-atom catalyst provided in the present disclosure may have excellent selectivity and anti-interference performance in the degradation of organic pollutants.

A portable oxygen concentrator includes at least one separation mechanism and an oxygen storage tank, where the separation mechanism is connected to the oxygen storage tank and includes an air bag and a molecular sieve tank that is filled with a molecular sieve for adsorption. The air bag has an air inlet and an air outlet. The air bag is connected to the molecular sieve tank through a valve group, which includes a first single valve and a second single valve. The air bag is connected to the molecular sieve tank through the first single valve. Each of the two ends of the molecular sieve tank has at least one gas outlet. When an inner space of the air bag is compressed and expanded once, the molecular sieve in the molecular sieve tank adsorbs and desorbs once.

An active oxygen supply device that is a plasma actuator equipped with a plasma generator and an ultraviolet light source in a housing having at least one opening, the plasma generator being provided with a first electrode and a second electrode with a dielectric in-between and creating an induced flow that contains ozone by applying a voltage between the two electrodes, in which the plasma actuator is positioned so that the induced flow flows outside the housing from an opening, and the ultraviolet light source irradiates the induced flow with ultraviolet rays and generates active oxygen in the induced flow; a device for conducting treatment by active oxygen; and a method for conducting treatment by active oxygen.

Metal oxide particles having: (1) a volume ratio (a) in 0.7 μm band of 5 to 40 vol %, (2) a volume ratio (b) in 13 μm band of 20 to 45 vol %, (3) a volume ratio (c) in 1.3 μm band of 20 to 50 vol %, and (4) a sum of the volume ratios (a), (b), and (c) of 60 to 100 vol %. The 0.7 μm, 13 μm, and 1.3 μm bands are particle size distributions having peaks at 0.3 to 1.2 μm, 0.3 to 20 μm, and 0.7 to 3 μm, respectively. The volume ratios (a), (b), and (c) of each band have peaks near 0.7 μm, 1.3 μm, and 13 μm in a particle size distribution curve, and being obtained by calculating an abundance ratio of particles in each band from a numerical integration of distribution curves obtained by further dividing the particle size distribution curve into three bands.

Provided is a method for producing a photocatalyst electrode for water decomposition that exhibits excellent detachability between the substrate and the photocatalyst layer and exhibits high photocurrent density. The method for producing a photocatalyst electrode for water decomposition of the invention includes: a metal layer forming step of forming a metal layer on one surface of a first substrate by a vapor phase film-forming method or a liquid phase film-forming method; a photocatalyst layer forming step of forming a photocatalyst layer by subjecting the metal layer to at least one treatment selected from an oxidation treatment, a nitriding treatment, a sulfurization treatment, or a selenization treatment; a current collecting layer forming step of forming a current collecting layer on a surface of the photocatalyst layer, the surface being on the opposite side of the first substrate; and a detachment step of detaching the first substrate from the photocatalyst layer.