The present specification relates to a carrier-nanoparticle complex, a method for preparing the same, and a catalyst comprising the same.

The present specification relates to a carrier-nanoparticle complex, a method for preparing the same, and a catalyst comprising the same.

Disclosed herein are methods for synthesizing 1,2,5,6-hexanetetrol (HTO), 1,6 hexanediol (HDO) and other reduced polyols from C5 and C6 sugar alcohols or R glycosides. The methods include contacting the sugar alcohol or R-glycoside with a copper catalyst, most desirably a Raney copper catalyst with hydrogen for a time, temperature and pressure sufficient to form reduced polyols having 2 to 3 fewer hydoxy groups than the starting material. When the starting compound is a C6 sugar alcohol such as sorbitol or R-glycoside of a C6 sugar such as methyl glucoside, the predominant product is HTO. The same catalyst can be used to further reduce the HTO to HDO.

Disclosed herein are methods for synthesizing 1,2,5,6-hexanetetrol (HTO), 1,6 hexanediol (HDO) and other reduced polyols from C5 and C6 sugar alcohols or R glycosides. The methods include contacting the sugar alcohol or R-glycoside with a copper catalyst, most desirably a Raney copper catalyst with hydrogen for a time, temperature and pressure sufficient to form reduced polyols having 2 to 3 fewer hydoxy groups than the starting material. When the starting compound is a C6 sugar alcohol such as sorbitol or R-glycoside of a C6 sugar such as methyl glucoside, the predominant product is HTO. The same catalyst can be used to further reduce the HTO to HDO.

The invention relates to a multi-stage medical sewage sterilization device and method based on graphene nano technologies. The multi-stage sterilization device comprises multiple stages of graphene nano composite sterilization grids, a graphene photocatalytic sterilization tank, a graphene-modified diatom ceramic disinfection tank, an ultrasonic sterilization tank and a laser and near-infrared sterilization device. Compared with a traditional method, the present invention has a more thorough killing or blocking effects on pathogenic bacteria, parasite eggs and the like in various medical sewages. In addition, the device of the present invention can be disassembled and cleaned regularly, and has a long service life, thus the process cost is reduced.

Provided are a noble metal-transition metal complex catalyst supported on a carbon-coated silica-alumina support and a preparation method therefor, the catalyst being capable of obtaining a fast reaction rate and catalyst stability, as compared to a conventional catalyst, when cyclohexane dimethanol (CHDM) production is carried out by a cyclohexane dicarboxylic acid (CHDA) hydrogenation reaction in an aqueous solution by using a carbon-coated supported catalyst.

The present subject matter relates generally to the derivatization of highly-aligned carbon nanotube sheet substrates with one or more transition metal centers and to uses of the resulting metal-derivatized CNT sheet substrates.

The present subject matter relates generally to the derivatization of highly-aligned carbon nanotube sheet substrates with one or more transition metal centers and to uses of the resulting metal-derivatized CNT sheet substrates.

The invention discloses a visible light responsive titanium dioxide nanowire/metal organic skeleton/carbon nanofiber membrane and preparation method and application thereof. A CNF (Carbon Nano Fiber)/TiO.sub.2 nano-wire/MIL-100 (represented as CTWM) membrane material is prepared and an MIL-100 material is used for adsorbing waste gas to enhance the photocatalytic effect of titanium dioxide on the membrane material; a CNF/TiO.sub.2/MIL-100 membrane catalyst sufficiently utilizes the adsorption capability of MIL-100 on the waste gas, the photocatalytic degradation performance of the TiO.sub.2 and high electrical conductivity of CNF to effectively prolong the service life of photoelectrons and promote the photocatalytic activity of the photoelectrons.

Embodiments of the present disclosure include a hyperpolarizing system, comprising a hyperpolarization reaction chamber having a location therein for supporting a solid catalyst with a sample in contact therewith, a cooler configured to lower a temperature of the sample and the solid catalyst to a temperature in a range of about 70K and about 250K, and an optical light source configured to direct light energy toward the solid catalyst to thereby hyperpolarize electrons in the solid catalyst and facilitate transfer of hyperpolarization to nuclei of the sample.