Abstract: Provided is a preparation method for a tube. The method comprises the following steps: a) adding a polymer solution into a poor solvent, such that the polymer diffuses on the liquid level of the poor solvent, so as to obtain a polymer film, wherein the solvent in the polymer solution is dissolved in the poor solvent; b) curling the polymer film on the liquid level of the poor solvent by using a mold to obtain a bar; and c) removing the mold to obtain a tube. The present invention further provides the use of the above tubular as an artificial tubular tissue.

Abstract: Provided is a method for preparing a crosslinked polyvinyl chloride structure foamed material by using a physical foaming agent, comprising: melting and mixing a polyvinyl chloride resin, a modified resin, an isocyanate, an anhydride, a nucleating agent and a heat stabilizer to obtain a blank; immersing the blank into a foaming gas for foaming to obtain a foamed body; and subjecting the foamed body to crosslinking curing to obtain a crosslinked polyvinyl chloride structure foamed material. According to the present invention, the crosslinked polyvinyl chloride structure foamed material is prepared by means of a brand-new process route, and the composition and proportion of the PVC resin and other raw materials can be adjusted in a wide range; and carbon dioxide or nitrogen is used for foaming. Further provided is a crosslinked polyvinyl chloride structure foamed material.

Abstract: The invention discloses an electrochemical device for treating cancer, characterized by using an acupuncture needle as a working electrode to produce hydrogen in a tumor tissue, thereby destroying the tumor tissue through the produced hydrogen gas. The device of the invention has low cost and simple operation, can realize minimally invasive treatment, and is green and environmentally friendly.

Abstract: The present disclosure provides a medical adhesive and a preparation method thereof, comprising a component A and a component B: the component A comprises a cycloketene acetal compound and an oxidizing agent; the component B comprises a vinyl monomer, a cross-linking agent and a reducing agent, wherein the cycloketene acetal compound is selected from one or more of 2-methylene-1,3-dioxepane, 2-methylene-4-phenyl-1,3-dioxolane, 5,6-benzo-2-methylene-1,3-dioxepane and 4,7-dimethyl-2-methylene-1,3-dioxepane. The medical adhesive overcomes the disadvantages of conventional medical adhesives.

Abstract: The invention discloses an electrochemical device for treating cancer, characterized by using an acupuncture needle as a working electrode to produce hydrogen in a tumor tissue, thereby destroying the tumor tissue through the produced hydrogen gas. The device of the invention has low cost and simple operation, can realize minimally invasive treatment, and is green and environmentally friendly.

Abstract: Carbon dioxide-reversibly-protected chain extension-crosslinking agents and a preparation method and use thereof are disclosed, The carbon dioxide-reversibly-protected chain extension-crosslinking agents have chemical structures represented by Formula I, Formula II, Formula III or Formula IV, wherein, n, m and p are integers, R is either OCH2CH(CH3) or OCH2CH2, 1?n?20, 1?m?10, and 1?p?10.

Abstract: The present disclosure relates to a method for preparing an ordered porous carbon materials with inexpensive carbon black. The method comprises: dispersing carbon black into a concentrated nitric acid to obtain a uniform dispersion; placing the dispersion in a reactor to perform a reaction by a one-step hydrothermal process; and washing and drying the reaction mixture to obtain an ordered porous carbon material in a honeycomb-like arrangement and rich in oxygen defects. The present disclosure also relates to an ordered porous carbon material prepared by the method, a method for electrocatalytically reducing carbon dioxide to formic acid under ambient temperature and atmospheric pressure by using the ordered porous carbon material, and a method for electrocatalytically reducing nitrogen to ammonia under ambient temperature and atmospheric pressure by using the ordered porous carbon material as a supported catalyst.

Abstract: The present disclosure provides a method for efficiently inducing phase separation of a water-organic solvent mixed solution through an inorganic salt, comprising the following steps: A) adding the inorganic salt to the water-organic matter mixed solution, sonicating and then allowing to stand for complete dissolution of the inorganic salt, wherein the water-organic matter mixed solution is a water-acetonitrile mixed solution or a water-acetone mixed solution; the inorganic salt is one or more of LiCl, NaCl, KCl, CsCl, NaBr, KBr, Li2SO4, Na2SO4 and MgSO4; B) allowing the solution obtained in the step A) to stand in a constant temperature environment until phase separation is completed to obtain a product.

Abstract: The present invention provides a chlorinated poly(propylene carbonate)/biomass composite material, comprising 3 wt % to 57 wt % of a chlorinated poly(propylene carbonate); 40 wt % to 94 wt % of a biomaterial; 2 wt % to 20 wt % of a rosin or a rosin derivative; 0 wt % to 1 wt % of an antioxidant; and 0 wt % to 5 wt % of a filler, wherein a sum of amounts of all components is 100 wt %. The chlorinated poly(propylene carbonate) functions as a binder, and plays an important role in the moisture resistance of the composite material. The rosin or the rosin derivative functions as a viscosifier and a lubricant, and can also improve the moisture resistance and mechanical property of the composite material. Under the synergistic effect of the above components, the composite material obtained in the present invention is excellent in both mechanical property and moisture resistance.

Abstract: Carbon dioxide-reversibly-protected chain extension-crosslinking agents and a preparation method and use thereof are disclosed, The carbon dioxide-reversibly-protected chain extension-crosslinking agents have chemical structures represented by Formula I, Formula II, Formula III or Formula IV, wherein, n, m and p are integers, R is either OCH2CH(CH3) or OCH2CH2, 1?n?20, 1?m?10, and 1?p?10.

Abstract: The present disclosure relates to a preparation method and use of a thickness-controllable bismuth nanosheet and its alloy, in order to solve the technical problems that the existing metal catalysts for the conversion of carbon dioxide to formic acid exhibit a low efficiency, a high overpotential, a relatively positive hydrogen evolution potential, and a poor stability. In the present disclosure, a bismuth nanosheet of a single atom layer thickness with a thickness of only 0.7 nm is obtained through an aqueous solution reduction method by using a bismuth salt compound as a raw material, using ethylene glycol ethyl ether as a solvent, and using a highly reductive aqueous solution containing NaBH4, LiBH4 or the like as a reducing agent, under a protection atmosphere of an inert gas.

Abstract: The present disclosure provides a white organic electroluminescent device, comprising: a substrate; an anode layer; a first light emitting layer formed from a red organic fluorescent material, a first energy-sensitized organic material and a first hole-type organic host material; a second light emitting layer formed from a green organic fluorescent material, a second energy-sensitized organic material and a second hole-type organic host material; and a cathode layer.

Abstract: The present disclosure provides a blue organic electroluminescent device comprising: a substrate; an anode layer disposed on the substrate; a light emitting layer disposed on the anode layer, the light emitting layer being formed from a blue organic fluorescent material and a hole-type organic host material, wherein the blue organic fluorescent material is 8.0% to 25.0% by mass of the hole-type organic host material; and a cathode layer disposed on the light emitting layer.

Abstract: The invention provides a blue organic electroluminescent device, composed of a substrate, an anode layer, an anode modification layer, a hole transporting-electron blocking layer, a hole-dominated light-emitting layer, an electron-dominated light-emitting layer, a hole blocking-electron transporting layer, a cathode modification layer, and a cathode layer arranged in turn, wherein the electron-dominated light-emitting layer is composed of an organic sensitive material, a blue organic light-emitting material, and an electron-type organic host material.

Abstract: A copolymer of ethylene and a conjugated diene is provided, in which ethylene content in the copolymer is greater than 20 mol %, the copolymer has a glass transition temperature between ?110° C. and ?90° C., and continuous methylene sequence lengths (MSL) in the copolymer are in a range of 12-162 methylene units.

Abstract: The invention provides an anthracene-based organic dye and a preparation method thereof. The organic dye provided by the invention has a structure of formula (I) or formula (II), wherein Ra, Rb, and R2-1 to R2-4 are as defined herein. The organic dye provided by the invention is obtained by modifying an anthracene with Ra and Rb or modifying anthracene-based groups decorated with an aryl group or a heteroaryl group with Ra and Rb, thereby the power conversion efficiency of a dye sensitized solar cell is significantly improved when the organic dye prepared according to the present invention is applied in a dye-sensitized solar cell. Furthermore, the preparation method of the organic dye according to the present invention is quite simple together with abundant raw materials and low cost, making it possible to be commercialized.

Abstract: This invention provides a production method of a poly(carbonate-ether)polyol, comprising the steps of: performing a reaction between a carboxylic acid and an epoxide to obtain an intermediate, wherein the carboxylic acid has an acidity constant of 0.2 to 4; and performing a polymerization reaction between the intermediate and carbon dioxide under the action of a rare earth doped double metal cyanide of Zn3[Co(CN)6]2 to obtain a poly(carbonate-ether)polyol. In the production method of the poly(carbonate-ether)polyol provided by this invention, a carboxylic acid having a suitable acidity constant is used as an initiator and an epoxide is firstly activated by using the carboxylic acid, and polyethers having different molecular weights generated in situ after activation are used as chain transfer agents to be involved in the polymerization reaction between carbon dioxide and the epoxide under the action of a rare earth doped double metal cyanide Zn3[Co(CN)6]2.

Abstract: A fiber grating sensor insert, implanting system and method of an intelligent plastic pipe.

Abstract: This invention provides an orange-yellow-emitting phosphor, the preparation method and the use thereof. This orange-yellow-emitting phosphor has a general formula represented by formula I: Sr9?a?b?xMaMg1.5+b(PO4)7:xEu2+??formula I wherein in formula I, said M is one or two of Ca and Ba; and 0.001?x?0.9, 0?a?1.0, 0?b?2.3. This orange-yellow-emitting phosphor uses a phosphate as the host material and Eu2+ ions as activation ions. The chemical properties of the phosphor are stable. The phosphor has relatively wide excitation band and emission band. And the red component in its emission spectrum is abundant, therefore, coupling the blue InGaN chip with the orange-yellow-emitting phosphor provided by this invention can obtain warm white light. The phosphor is radiation free, therefore, it will not be harmful to the environment.

Abstract: A composite material packaged fiber grating sensor and a manufacturing method thereof. The sensor includes a fiber grating sensor component, a composite material coverage layer, a resin package layer and a composite material substrate layer. In the sensor, a temperature fiber grating and a strain fiber grating are packaged in a composite material structure, so that the structure is light and simple, its computability with the composite material is good, the measurement accuracy is high, and the survival rate and the service life of the installed sensor can be greatly improved, the sensor component can be externally pasted on to or inter-implanted in a composite material structural part, and can be applied to the distributed online health monitoring on the structural part. The manufacturing method of the composite material packaged fiber grating sensor is simple, efficient and stable, and is suitable for rapid mass production by enterprises.