A visible-light-photocatalyzed composite light-transmitting concrete contains several bundles of optical fibers, the optical fibers are coated with a protective layer on their outer surface, the protective layer contains a visible light photocatalyst, and the concrete has several gas-permeable pores. Such concrete is prepared by mixing a visible light photocatalyst and a light-transmitting glue, applying the mixture to the surface of optical fibers to form a protective layer, and using optical fibers in the concrete. The resulting concrete has dual properties of light transmittance and photocatalytic oxidation of gas-phase pollutants under visible light irradiation. The visible-light-photocatalyzed composite light-transmitting concrete significantly breaks through the limitation of photocatalytic concrete to light sources, so that gas-phase pollutants can be removed under visible light irradiation through photocatalysis of light-transmitting concrete. It also has good mechanical properties, decorativeness, and functional practicability due to coated optical fibers.

A visible-light-photocatalyzed composite light-transmitting concrete contains several bundles of optical fibers, the optical fibers are coated with a protective layer on their outer surface, the protective layer contains a visible light photocatalyst, and the concrete has several gas-permeable pores. Such concrete is prepared by mixing a visible light photocatalyst and a light-transmitting glue, applying the mixture to the surface of optical fibers to form a protective layer, and using optical fibers in the concrete. The resulting concrete has dual properties of light transmittance and photocatalytic oxidation of gas-phase pollutants under visible light irradiation. The visible-light-photocatalyzed composite light-transmitting concrete significantly breaks through the limitation of photocatalytic concrete to light sources, so that gas-phase pollutants can be removed under visible light irradiation through photocatalysis of light-transmitting concrete. It also has good mechanical properties, decorativeness, and functional practicability due to coated optical fibers.

Supported chromium catalysts with an average valence less than +6 and having a hydrocarbon-containing or halogenated hydrocarbon-containing ligand attached to at least one bonding site on the chromium are disclosed, as well as ethylene-based polymers with terminal alkane, aromatic, or halogenated hydrocarbon chain ends. Another ethylene polymer characterized by at least 2 wt. % of the polymer having a molecular weight greater than 1,000,000 g/mol and at least 1.5 wt. % of the polymer having a molecular weight less than 1000 g/mol is provided, as well as an ethylene homopolymer with at least 3.5 methyl short chain branches and less than 0.6 butyl short chain branches per 1000 total carbon atoms.

The invention relates to a process for adding an organic compound to a porous solid wherein the porous solid and the organic compound in the liquid state are brought together simultaneously, without physical contact between the solid and the organic compound in the liquid state, at a temperature below the boiling point of the organic compound and under pressure and time conditions such that a fraction of said organic compound is transferred gaseously to the porous solid.

The invention relates to a process for adding an organic compound to a porous solid wherein the porous solid and the organic compound in the liquid state are brought together simultaneously, without physical contact between the solid and the organic compound in the liquid state, at a temperature below the boiling point of the organic compound and under pressure and time conditions such that a fraction of said organic compound is transferred gaseously to the porous solid.

Processes for producing an activated chromium catalyst are disclosed, and these processes comprise contacting a supported chromium catalyst with a gas stream containing from 25-60 vol % oxygen at a peak activation temperature of 550-900° C. to produce the activated chromium catalyst. The linear velocity of the gas stream is 0.18-0.4 ft/sec, and the oxygen linear velocity of the gas stream is 0.05-0.15 ft/sec. The resultant activated chromium catalyst and an optional co-catalyst can be contacted with an olefin monomer and an optional olefin comonomer in a polymerization reactor system under polymerization conditions to produce an olefin polymer.

An ink composition, including a quantum dot; a metal catalyst; an aromatic halide compound; an ene compound including at least one C—H moiety and a carbon-carbon unsaturated bond; and optionally, a metal oxide particle, wherein the metal catalyst is a metal salt, a metal coordination complex, or a combination thereof, wherein the metal catalyst comprises a metal that is palladium, nickel, ruthenium, rhodium, iridium, iron, cobalt, chromium, copper, platinum, silver, gold, or a combination thereof.

An ink composition, including a quantum dot; a metal catalyst; an aromatic halide compound; an ene compound including at least one C—H moiety and a carbon-carbon unsaturated bond; and optionally, a metal oxide particle, wherein the metal catalyst is a metal salt, a metal coordination complex, or a combination thereof, wherein the metal catalyst comprises a metal that is palladium, nickel, ruthenium, rhodium, iridium, iron, cobalt, chromium, copper, platinum, silver, gold, or a combination thereof.

The present invention relates to a compound represented by the chemical formula 1, a catalyst system for olefin oligomerization comprising the same, and a method for oligomerizign olefins using the same, and the catalyst system for olefin oligomerization according to the present invention has excellent catalytic activity as well as high selectivity for 1-hexene or 1-octene, thereby enabling more efficient preparation of alpha-olefins.

The invention related to photocatalytic material field, and discloses a metal-doped amorphous carbon nitride photocatalytic material and the preparation method thereof. The method comprises: (1) mixing the nitrogen-rich organic matter with the metal salt; (2) calcining the mixture obtained in step (1) to obtain the photocatalytic material; the nitrogen-rich organic matter is selected from one or more of melamine, dicyandiamide, monocyanamide, thiourea, urea, hexamethylenetetramine, and biuret; the metal salt is selected from one or more of an alkali metal salt, an alkaline earth metal salt, and a transition metal salt. The method is simple, efficient, low-cost, requires no external catalyst, organic solvent and protective reagent, and does not require pretreatment of raw materials, and is a preparation method favorable for large-scale commercial production.