Abstract: It discloses a vanadium-titanium compound material with high thermal stability and high activity and a preparation method thereof. The vanadium-titanium compound material is mainly composed of vanadium oxide and titanium oxide, where the content of vanadium oxide is 0.5% to 30% by mass of the vanadium-titanium compound material, and the crystal form of titanium oxide in the vanadium-titanium compound material is one of anatase and TiO2(B) or a mixture thereof.

Abstract: The present invention discloses a ?-polylysine hydrogel and the preparation method and application of the as-described ?-polylysine hydrogel. The polylysine hydrogel is non-toxic to a recipient, and has biodegradability and biocompatibility. The wound tissue healing material prepared by the present invention can be used in wound tissue adhesion in an efficient, stable, safe manner.

Abstract: A chemical additive for calcium sulphoaluminate-modified Portland cement comprises the following substances: (a) at least one alkanolamine borate; (b) at least one organic alcohol; and (c) at least one saccharide or a derivative thereof; and the substances and water are sequentially mixed and stirred to obtain the chemical additive for calcium sulphoaluminate-modified Portland cement. The chemical additive for calcium sulphoaluminate-modified Portland cement provided by the invention has better effects of regulating the setting time of the calcium sulphoaluminate-modified Portland cement and improving the 3d/28d strength increase rate, and also has a grinding aid effect when being added during grinding.

Abstract: This invention discloses a method for preparing an antibacterial and dust-removal membrane. The method comprises the following steps: depositing a layer of nano-ZnO on the immersed membrane surface as the seed crystal with the atomic layer deposition instrument (ALD instrument); vertically immersing the membrane covered with nano-ZnO layer in a hydrothermal reactor filled with crystal growth solution, heating it for a period of time, taking the membrane out and cooling it to the room temperate, and removing it from the substrate; finally, heating this membrane in a drier, and purging it with nitrogen to remove the paraffin within the membrane pore to obtain the porous membrane with nano-ZnO arrays growing on the surface.

Abstract: A portable rapid detection device for heavy metal ions includes a card electrode and a thin-layer flow cell, wherein a three-electrode system of the card electrode is inserted in a micro-channel of the thin-layer flow cell; and heavy metal ions are detected by using an anodic stripping voltammetry (ASV), a solution to be detected flows by the surface of a working electrode in the micro-channel, and heavy metals are enriched and stripped on the surface thereof.

Abstract: It discloses a chemical regeneration method of oxidized coenzyme NAD(P)+ which is under an oxygen or air atmosphere condition, adding a catalytic amount of bridged flavin, and oxidizing NAD(P)H to obtain NAD(P)+. The catalyst for regeneration of cofactor is cheap and easily available small organic molecule having no noble metal; this regeneration system can regenerate NADH and NADPH; this regeneration system has a wide pH range and temperature range, being applicable to various oxidation reactions catalyzed by nicotinamide-dependent oxidoreductase.

Abstract: A method for preparing caprolactam by using a microreactor under Lewis acid catalysis, wherein a hydroxyl group in a cyclohexanone oxime is activated to obtain a cyclohexanone oxime sulfonates intermediate, then rearranged under Lewis acid catalysis to prepare the caprolactam. The method of this invention has a simple process and a high operation safety and selectivity, the reaction condition is mild, an efficient reaction can take place even at room temperature, the reaction time is short, the conversion of the cyclohexanone oxime can reach 100% within a short time, the selectivity of the caprolactam can reach 99%, the energy consumption is greatly reduced in the premise of maintaining a high yield, and the production cost is reduced, being an efficient and green and environmentally friendly method of for synthesizing the caprolactam.

Abstract: A method to prepare functional polyester polyols by using micro-reaction device, wherein mixing ?-caprolactone/?-valerolactone monomer with mercapto alcohol evenly with appropriate organic solution under moistureless conditions, and continuously transferring the prepared mixing solution into a micro-reaction device supported with an immobilized enzyme for polymerization to synthetize a poly (?-caprolactone/?-valerolactone). Compared with the prior art, the present invention achieves a continuous production by using immobilized lipase Novozyme435 as a catalyst.

Abstract: A hydrogel based on a cross-linked ?-polyglutamic acid and ?-polylysine polymer is obtained by cross-linking of ?-polyglutamic acid with ?-polylysine, and it is a polymer having the following constitutional unit, wherein, m is a natural number of 15 to 45, n is a natural number of 3900 to 17000, and x is a natural number of 5 to 40. It also discloses a preparation method of as-described hydrogel and its application in preparation as a medical wound dressing.

Abstract: A method for preparing a high-quality epoxidized fatty acid ester with a micro-reaction device, including: respectively pumping an aqueous hydrogen peroxide solution and a carboxylic acid at the same time into a first micro-mixer; after the reaction in the first micro-reactor, respectively pumping the output material and an unsaturated fatty acid ester into a second micro-mixer; completely mixing them and then introducing the mixture into a second micro-reactor; and after a complete reaction, water-rinsing the organic phase part of the resultant reaction liquid and drying the same to obtain the epoxidized fatty acid ester.

Abstract: A method for preparing caprolactam by using a microreactor under Lewis acid catalysis, wherein a hydroxyl group in a cyclohexanone oxime is activated to obtain a cyclohexanone oxime sulfonates intermediate, then rearranged under Lewis acid catalysis to prepare the caprolactam. The method of this invention has a simple process and a high operation safety and selectivity, the reaction condition is mild, an efficient reaction can take place even at room temperature, the reaction time is short, the conversion of the cyclohexanone oxime can reach 100% within a short time, the selectivity of the caprolactam can reach 99%, the energy consumption is greatly reduced in the premise of maintaining a high yield, and the production cost is reduced, being an efficient and green and environmentally friendly method of for synthesizing the caprolactam.

Abstract: The present invention discloses a ?-polylysine hydrogel and the preparation method and application of the as-described ?-polylysine hydrogel. The polylysine hydrogel is non-toxic to a recipient, and has biodegradability and biocompatibility. The wound tissue healing material prepared by the present invention can be used in wound tissue adhesion in an efficient, stable, safe manner.

Abstract: A method for regenerating a Cu-BTC material includes: impregnating a Cu-BTC adsorbed with guest molecules in an acidic proton solvent or in a steam environment thereof, and filtering the Cu-BTC material, to obtain a solid; impregnating the solid in a non-acidic organic solvent or a steam environment thereof, and finally filtering, washing and drying the solid, to complete the generation of the Cu-BTC material.

Abstract: It discloses a use of N-acetylneuraminic acid aldolase with an amino acid sequence as shown in SEQ ID NO: 2 in catalytic synthesis of N-acetylneuraminic acid. The preparation of N-acetylneuraminic acid is to use the N-acetylneuraminic acid aldolase with the amino acid sequence as shown in SEQ ID NO: 2 as a catalyst, and N-acetylmannosamine and pyruvic acid as substrates.

Abstract: A method for preparing a high-quality epoxidized fatty acid ester with a micro-reaction device, including: respectively pumping an aqueous hydrogen peroxide solution and a carboxylic acid at the same time into a first micro-mixer; after the reaction in the first micro-reactor, respectively pumping the output material and an unsaturated fatty acid ester into a second micro-mixer; completely mixing them and then introducing the mixture into a second micro-reactor; and after a complete reaction, water-rinsing the organic phase part of the resultant reaction liquid and drying the same to obtain the epoxidized fatty acid ester.

Abstract: The methods for preparing Cu-BTC and nano-Cu-BTC are disclosed. An imporous coordination compound Cu(C9H4O6)(H2O)3 is impregnated an organic solvent or a steam environment thereof to obtain Cu-BTC. Cu-BTC is impregnated in an acidic protic solvent environment and filtered to obtain a solid, and the solid is impregnated in a non-acidic organic solvent or a steam environment thereof, centrifuged, washed, and dried, to obtain nano-Cu-BTC.

Abstract: The methods for preparing Cu-BTC and nano-Cu-BTC are disclosed. An imporous coordination compound Cu(C9H4O6)(H2O)3 is impregnated an organic solvent or a steam environment thereof to obtain Cu-BTC. Cu-BTC is impregnated in an acidic protic solvent environment and filtered to obtain a solid, and the solid is impregnated in a non-acidic organic solvent or a steam environment thereof, centrifuged, washed, and dried, to obtain nano-Cu-BTC.

Abstract: A method for regenerating a Cu-BTC material includes: impregnating a Cu-BTC adsorbed with guest molecules in an acidic proton solvent or in a steam environment thereof, and filtering the Cu-BTC material, to obtain a solid; impregnating the solid in a non-acidic organic solvent or a steam environment thereof, and finally filtering, washing and drying the solid, to complete the generation of the Cu-BTC material.

Abstract: It discloses a vanadium-titanium compound material with high thermal stability and high activity and a preparation method thereof. The vanadium-titanium compound material is mainly composed of vanadium oxide and titanium oxide, where the content of vanadium oxide is 0.5% to 30% by mass of the vanadium-titanium compound material, and the crystal form of titanium oxide in the vanadium-titanium compound material is one of anatase and TiO2(B) or a mixture thereof.