Patent classifications
B01J31/126
Novel Antimicrobial Topical Skin Closure Compositions and Systems
Novel compositions and systems for closure of wounds with antimicrobial effectiveness are disclosed. The compositions provide devices of improved flexibility and elasticity and are readily applied to wound sites or over wound closure devices. The present invention is also directed to a novel platinum catalyst for use in such compositions. The catalyst provides for rapid curing on topical surfaces such as skin and bonds to such surfaces in about 2-5 minutes.
HYBRID MATERIAL AND METHOD FOR THE PRODUCTION THEREOF
The invention relates to a material in the form of a cellular solid monolith consisting of an inorganic oxide polymer. Said monolith comprises macropores which have an average size d.sub.A of 4 μm to 50 μm, mesopores that have an average size d.sub.E of 20 to 30 Å, and micropores which have an average size d.sub.1 of 5 à 10 Å, said pores being interconnected. The inorganic oxide polymer has organic groups R of formula —(CH.sub.2).sub.n—R.sup.1, wherein 0≤n≤5, and R.sup.1 is selected from among a thiol group, a pyrrole group, an amino group having one or more optional, optionally substituted alkyl, alkylamino, or aryl substituents, an alkyl group, or a phenyl group optionally having an alkyl-type substituent R.sup.2. The disclosed material can be used as a substrate for a metal catalyst and for decontaminating liquid or gaseous media.
Filter containing photocatalyst particles and resin particles
A filter includes resin particles and photocatalyst particles having absorption at wavelengths of 450 nm and 750 nm in the visible absorption spectrum. The photocatalyst particles have a high photocatalytic function and are present on the surface of the resin particle. The filter is air permeable, transmits visible light, and has high deodorizing performance.
FILTER
A filter includes resin particles and photocatalyst particles having absorption at wavelengths of 450 nm and 750 nm in the visible absorption spectrum. The photocatalyst particles are present on the surface of the resin particle.
Method for preparing 2,5-dimethylfuran by directly catalyzing carbohydrate using modified Pd/C
A preparation method of an acidic and hydrophobic Pd/C catalytic material comprises performing a simple treatment with chlorosulfonic acid and trimethylchlorosilane, washing and drying a treatment product to obtain a modified Pd/C catalytic material. A method for preparing 2,5-methylfuran by catalyzing a carbohydrate with modified Pd/C comprises: dissolving the carbohydrate in alcohol, allowing a reaction to proceed with modified Pd/C as a catalyst and polymethylhydrosiloxane as a hydrogen donor at a temperature of 80140 C. for 1-5 hours, and performing centrifugation to separate the catalyst from the product. The content of the modified Pd/C content is 1-3 mol % relative to the carbohydrate; the polymethylhydrosiloxane amount is equivalent to 4-10 times the carbohydrate amount, and the carbohydrate concentration in the alcohol is 2-6 wt %. The method overcomes the defect of being difficult to prepare the 2,5-methylfuran by directly catalyzing the carbohydrate, and features moderate reaction conditions and high activity.
METHOD FOR PREPARING 2,5-DIMETHYLFURAN BY DIRECTLY CATALYZING CARBOHYDRATE USING MODIFIED PD/C
A preparation method of an acidic and hydrophobic Pd/C catalytic material comprises performing a simple treatment with chlorosulfonic acid and trimethylchlorosilane, washing and drying a treatment product to obtain a modified Pd/C catalytic material. A method for preparing 2,5-methylfuran by catalyzing a carbohydrate with modified Pd/C comprises: dissolving the carbohydrate in alcohol, allowing a reaction to proceed with modified Pd/C as a catalyst and polymethylhydrosiloxane as a hydrogen donor at a temperature of 80140 C. for 1-5 hours, and performing centrifugation to separate the catalyst from the product. The content of the modified Pd/C content is 1-3 mol % relative to the carbohydrate; the polymethylhydrosiloxane amount is equivalent to 4-10 times the carbohydrate amount, and the carbohydrate concentration in the alcohol is 2-6 wt %. The method overcomes the defect of being difficult to prepare the 2,5-methylfuran by directly catalyzing the carbohydrate, and features moderate reaction conditions and high activity.
High activity catalyst for hydrosilylation reactions and methods of making the same
A heterogeneous catalyst comprising a metal-containing polymer matrix covalently bonded to a support material and a method of making and using such catalysts. The metal-containing polymer matrix comprises metal nano-particles encapsulated in a polymer matrix, e.g., a siloxane. In one aspect, the metal-containing polymer matrix can be bonded to the support material via a hydrophobic group attached to the support material. The catalyst can be recovered after being used in a metal catalyzed reaction and exhibit excellent catalytic activity upon reuse in subsequent reactions.