A method of reducing a carbon oxide to a lower oxidation state by providing a solution of a metal acetate in a solvent in a reaction vessel, evaporating the solvent to leave a film of the metal acetate on an interior surface of the reaction vessel, and reacting a carbon oxide with a gaseous reducing agent in the reaction vessel to produce a solid carbon product on the metal acetate is disclosed. Another method includes dispersing particles in a gas. The particles include a solution of a metal acetate in a solvent. The solvent is evaporated to form particles including the metal acetate. An apparatus includes a capillary tube configured to receive and emit a solution, an electrode, and a voltage source connected to the capillary tube, the voltage source having a higher potential than the electrode.

Described herein is a supported organotin catalyst and a preparation method for a sucrose-6-carboxylate. The supported organotin catalyst is prepared by coupling an organotin functional group to an inorganic carrier. The supported organotin catalyst of the present application can be used for catalyzing the generation of a sucrose-6-carboxylate, and after reaction, the supported organotin catalyst can be directly filtered and recovered only by adding a small amount of water to quench an acylating agent, so that the subsequent dehydration process is simpler and easier, and the supported organotin catalyst is thus very economical in terms of manpower, equipment and energy.

The invention is related to the sphere technologies for desulfurization and demercaptanization of gaseous hydrocarbons. It can be used for purification of any gaseous hydrocarbon medium. The device includes a catalytic reactor loaded with a catalyst solution in an organic solvent, a means of withdrawal sulfur solution from the reactor into the sulfur-separating unit, and a sulfur-separating unit. The sulfur-separation unit includes a means of sulfur extraction. The reactor design and the catalyst composition provide conversion of at least 99.99% of hydrogen sulfide and mercaptans into sulfur and disulfides. The catalyst is composed of mixed-ligand complexes of transition metals. The technical result achieved by use of claimed invention is effectively a single-stage purification of gaseous hydrocarbons from hydrogen sulfide and mercaptans with remaining concentration of SH down to 0.001 ppm while leaving no toxic waste.

Titania-based porous nanoparticle coatings are mechanically robust, with low haze, which exhibit short time scales for decomposition of fingerprint oils under ultraviolet light. The mechanism by which a typical dactylogram is consumed combines wicking of the sebum into the nanoporous titania structure followed by photocatalytic degradation. These TiO.sub.2 nanostructured surfaces are also anti-fogging, anti-bacterial, and compatible with flexible glass substrates and remain photocatalytically active in natural sunlight.

A porous catalyst for catalytic activating persulfates to decompose typical pollutants in papermaking wastewater is provided, and a synthesis method thereof and a method of degrading the typical pollutants in paper wastewater by using the porous catalyst are also provided. The porous catalyst MIL-88A@MIP is prepared by a molecular imprinting method comprising using metal organic framework MIL-88A as a precursor and using phthalates as templates.

Aspects of the present disclosure include compositions comprising iminium catalyst, methods of making, methods of using, and the like.

A sensor can include one or more of a semiconducting material, an oxidation catalyst, and an oxidation enhancer, the sensor being configured to detect an analyte, such as methane, a thiol, or both.

The invention discloses a method for preparing maleate by selective catalytic oxidation of lignin. The method uses a heteropolyacid functionalized ionic liquid as a catalyst, and an aqueous alcohol solution as a reaction medium to achieve high-efficiency selective catalytic conversion and ring opening oxidation of biomass lignin at a reaction temperature of 110-160 C. and an oxygen pressure of 0.5-1.0 MPa for 1-6 h. The selectivity of maleate is higher than 47.83%. The yield and selectivity of a single chemical derived from the depolymerization of lignin in the present invention are much higher than the prior art, and the ionic liquid catalyst exhibits outstanding advantages such as availability of recovery and recycling through simple temperature adjustment; the reaction conditions of the present invention are mild, and the process is green and safe, easy to operate, and available forbatch and continuous production. The invention provides a new green way for preparing bulk chemicals like maleate from reproducible raw materials such as lignin.

Provided is a liquid hydrogen storage material including 1,1-biphenyl and 1,1-methylenedibenzene, the liquid hydrogen storage material including the corresponding 1,1-biphenyl and 1,1-methylenedibenzene at a weight ratio of 1:1 to 1:2.5. The corresponding liquid hydrogen storage material has excellent hydrogen storage capacity value by including materials having high hydrogen storage capacity, and is supplied in a liquid state, and as a result, it is possible to minimize initial investment costs and the like required when the corresponding liquid hydrogen storage material is used as a hydrogen storage material in a variety of industries.

Disclosed herein are reaction compositions comprising an oxidation catalyst, a solvent, and a substrate that is dissolved in the solvent. The oxidation catalyst comprises a metal ion complexed with an -keto acid and a tridentate N,N,O-ligand. Also disclosed herein are methods for oxidizing a CH bond of a molecule, the methods comprising contacting the molecule with a metal complex comprising a metal ion complexed with a tridentate N,N,O-ligand in the presence of an -keto acid and a solvent. In some embodiments, the oxidation catalyst or metal complex is linked to a solid support.