Abstract: A laser shock peening apparatus for the surface of a workpiece, said apparatus comprising a resonant cavity. When said apparatus is used to conduct laser shock peening, because of the presence of the resonant cavity, shock waves that would typically escape outward may instead be utilized, and composite shock waves may be formed as a result of the wave reflection and convergence effects of the resonant cavity. Said waves can then be used on the surface of a workpiece twice or multiple times, thereby greatly increasing energy utilization rates. In addition, a fluid-based confinement layer is limited to the inside of the resonant cavity and has a fixed shape, thereby effectively solving the problems of the poor stability of a fluid-based confinement layer and the difficulty with controlling the thickness of such a confinement layer.

Abstract: The present invention discloses a two-dimensional nanomaterial dispersant, a preparation method of a two-dimensional nanomaterial by liquid phase exfoliation, and use thereof.

Abstract: The present disclosure discloses a hexagonal boron nitride epoxy compound anticorrosive paint, and a preparation method and use thereof. The anticorrosive paint mainly comprises hexagonal boron nitride, an oligoaniline or polyaniline nanofiber, an epoxy resin, a dispersing medium, a paint additive, an epoxy resin curing agent, and a solvent. The hexagonal boron nitride epoxy compound anticorrosive paint provided by the present disclosure has the advantages, such as good stability, simple preparation process, and low cost, does not tend to precipitate, is suitable for large-scale production, forms a coating that has excellent barrier properties and lasting corrosion resistance, and has very good application prospects in the industries, such as chemical industry, petroleum, electric power, shipping, light textile, storage, transport, and spaceflight.

Abstract: The present disclosure provides a method for dispersing graphene. The method includes the following steps: providing a graphene material and a graphene dispersant, wherein the graphene dispersant comprises aniline oligomer or aniline oligomer derivative, the aniline oligomer or aniline oligomer derivative is an electroactive polymer, and the aniline oligomer or aniline oligomer derivative is able to combine with the graphene material via ?-? bond; and adding the graphene material and the graphene dispersant to a dispersing medium, making the aniline oligomer or aniline oligomer derivative combine with the graphene material via ?-? bond, and dispersing the graphene material in the dispersing medium by the graphene dispersant.

Abstract: A detection analyzer including a first sample input/output element, a second sample input/output element, a sample compartment, a vibration platform, a vibration generator, a data acquisition system, a laser converter, and a data display. The first sample input/output element and the second sample input/output element are each connected to the sample compartment; the vibration platform is located inside the sample compartment; the vibration generator is located outside the sample compartment, and the vibration platform is connected to the vibration generator; the data acquisition system is located outside the sample compartment, and is connected to the vibration platform; and the data display is connected to the data acquisition system.

Abstract: A polylactic acid nano-fiber membrane and preparation method thereof. In particular, the membrane has PLA nanofibers with an average diameter between 50 nm and 200 nm, wherein the nanofibers contain a crystal phase with a volume fraction between 45% and 85% and the crystal phase contains PLA stereocomplex crystals with a volume fraction between 85% and 95%. The method of preparation includes mixing dried PDLA and PLLA in a specific PLLA/PDLA ratio of between 95/5 and 99/1; producing continuous fibers or nonwovens in a extrusion and spinning device, and producing woven fabrics or nonwovens with the continuous fibers; heat treating the woven fabrics or nonwovens; washing the heat treated woven fabrics or nonwovens with a solvent; removing the solvent and drying the woven fabrics or nonwovens; and pressing the dried woven fabrics or nonwovens for making the membrane.

Abstract: Disclosed is a method for an all-laser hybrid additive manufacturing. After a matrix is obtained by means of selective laser melting forming, a subtractive forming is carried out on the matrix by means of a pulse laser to form a cavity, and the cavity is then packaged to obtain a forming material with an internal cavity structure. A laser precision packaging method is used in the method based on the melting of the laser selective region. Also disclosed is the apparatus, comprising a laser unit (2), a control unit (4) and a forming unit (6). The laser unit is in light path connection with the forming unit, and the control unit is electrically connected with the laser unit and the forming unit respectively. The laser unit comprises a first laser light source to and a second laser light source. The forming unit comprises a welding unit (68), and the welding unit is controlled by the control unit and is matched with the laser unit for the additive manufacturing.

Abstract: A polylactic acid nano-fiber membrane and preparation method thereof. In particular, the membrane has PLA nanofibers with an average diameter between 50 nm and 200 nm, wherein the nanofibers contain a crystal phase with a volume fraction between 45% and 85% and the crystal phase contains PLA stereocomplex crystals with a volume fraction between 85% and 95%. The method of preparation includes mixing dried PDLA and PLLA in a specific PLLA/PDLA ratio of between 95/5 and 99/1; producing continuous fibers or nonwovens in a extrusion and spinning device, and producing woven fabrics or nonwovens with the continuous fibers; heat treating the woven fabrics or nonwovens; washing the heat treated woven fabrics or nonwovens with a solvent; removing the solvent and drying the woven fabrics or nonwovens; and pressing the dried woven fabrics or nonwovens for making the membrane.

Abstract: The present invention provides a graphene composite powder form material that is suitable for industrialized application. The graphene composite powder form material is composited by graphene materials and a high-molecular compound. The high-molecular compound is uniformly coated on surfaces of the graphene material. Any adjacent graphene materials are separated by the high-molecular compound. An apparent density of the graphene composite powder form material is larger than or equal to 0.02 g/cm3. Under an external pressure, the graphene materials in the graphene composite powder form material do not re-stack, and can be easily restored to original form, which benefit the storage and transportation. Besides, the graphene composite powder form material has a good compatibility in other material systems, which greatly broadens the application fields in the downstream products and successfully solves the problem in industrial application.

Abstract: Provided in the present invention are a battery paste, a battery electrode plate, and a preparation method therefor, the battery electrode plate comprising a current collector and an electrode paste film attached to the current collector; the electrode paste film comprises an active substance, a conductive agent, a polymer binder, and fluorophosphate Compared to the prior art, by means of adjusting the components of the electrode paste film, prepared battery electrode plates of the present invention, particularly thick electrode plates, have excellent recycling performance and high rate charge and discharge performance; the preparation method is simple, easy to execute, and low cost, can incorporate existing production devices, and is suitable for use in industrial production; in addition, the battery electrode plate of the present invention contains fluorophosphate, which has a fire retardant effect and can improve the safety of lithium ion batteries MZ+[POxFy]Z??(I)

Abstract: A stack array in a solid oxide fuel cell power generation system is provided. The stack array comprises a supporting body and a stack group, wherein the supporting body is in a layered structure and comprises one layer or at least two layers of supporting units; and on each layer of the supporting units, a plurality of stacks are sequentially arranged to form the stack group, and each stack is horizontal, and fasteners are provided between the stacks to enable the stack groups and the supporting units to form a pressurized fastening structure. The stack array of the present disclosure simplifies the arrangement of pipelines in the related art, enables effective pressurized fastening on the stacks, so as to allow the whole stack array to be compact and steady, while facilitating the detach, repair and maintenance of the stacks, which is favorable for the integration of the system.

Abstract: Disclosed is a method for preparing a 2,5-disubstituted furan compound. The 2,5-disubstituted furan compound is prepared in a simple, convenient and highly efficient way by reacting 2,3-dicarboxylic anhydride-7-oxabicyclo[2.2.1]hept-5-ene and/or furan with an acylating reagent and/or an alkylating reagent. The preparation method is simple and efficient, has a short process and less by-products, and the 2,5-disubstituted furan compound prepared by using the method has a high purity, and can satisfy the requirements for being used as a raw material for engineering plastics, such as high-performance polyesters, epoxy resins, polyamides, polyurethanes and the like, and as a chemical raw material and a pharmaceutical intermediate raw material.

Abstract: The present invention relates to a modified lithium ion battery anode material having high energy density, and a manufacturing process thereof, the anode material comprising, from inside to outside, a core, a transition layer and a shell layer. The anode material of the present invention has the advantages of high energy density, low surface activity, good storage performance, and a simple manufacturing process, and is suitable for large scale application.

Abstract: The present invention provides a graphene coating-modified electrode plate for lithium secondary battery, characterized in that, the electrode plate comprises a current collector foil, graphene layers coated on both surfaces of the current collector foil, and electrode active material layers coated on the graphene layers. A graphene coating-modified electrode plate for lithium secondary battery according to the present invention comprises a current collector foil, graphene layers coated on both surfaces of the current collector foil, and electrode active material layers coated on the graphene layers. The graphene-modified electrode plate for lithium secondary battery thus obtained increases the electrical conductivity and dissipation functions of the electrode plate due to the better electrical conductivity and thermal conductivity of graphene. The present invention further provides a method for producing a graphene coating-modified electrode plate for lithium secondary battery.

Abstract: Provided is a positive electrode material for a lithium battery with an atomic ratio expressed by the formula (I) Lia(MxMn2-x)(O4-yZy) for 0.8?a?1.2, 0?x?1 and 0?y?1 in which M is one or more of Li, Na, K, Ca, Mg, Al, Ti, Sc, Ge, V, Cr, Zr, Co, Ni, Zn, Cu, La, Ce, Mn, Hf, Nb, Ta, Mo, W, Ru, Ag, Sn, Pb and Si and Z is one or more of OH, halogens, N, P, S and O, and the primary particles of the positive electrode material have a spheroidal topography. The adjacent (111) family planes of the primary particles are connected by curved surfaces without obvious edges. A preparing method of a positive electrode material for a lithium battery and a lithium battery are also provided. The positive electrode material of the present invention provides a good high-temperature cycling performance and filling capability.

Abstract: Described herein are solid solution composites that are used as cathode materials for lithium-ion batteries. The solid solution composite of ? LiMVO4-?LiNi1-x-yCoxMnyO2, in which LiMVO4 has cubic close-packed structure, LiNi1-x-yCoxMnyO2 has hexagonal layered structure, and both share an oxygen lattice fully or partly. The new solid solution materials have advantage for lithium-ion batteries that the working voltage of the composite is adjustable by controlling the molar ratio of ? and ? and have higher working voltage than current secondary battery materials. Also described herein are methods of preparing such composite.

Abstract: Disclosed is a method for preparing a 2,5-disubstituted furan compound. The 2,5-disubstituted furan compound is prepared in a simple, convenient and highly efficient way by reacting 2,3-dicarboxylic anhydride-7-oxabicyclo[2.2.1]hept-5-ene and/or furan with an acylating reagent and/or an alkylating reagent. The preparation method is simple and efficient, has a short process and less by-products, and the 2,5-disubstituted furan compound prepared by using the method has a high purity, and can satisfy the requirements for being used as a raw material for engineering plastics, such as high-performance polyesters, epoxy resins, polyamides, polyurethanes and the like, and as a chemical raw material and a pharmaceutical intermediate raw material.

Abstract: The present invention relates to a novel phosphate based composite anode material, preparation method and uses thereof. Specifically disclosed is a phosphate based composite cell anode material, the material having monoclinic and orthorhombic crystal lattice structures with the chemical formula of A3?xV2?yMY(PO4)3, wherein A is Li+, Na+ or the mixture thereof, M is Mg, Al, Sc, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn or Nb, 0?x?3.0, 0?y?2.0, and C is the carbon layer. Also disclosed are a preparation method and uses of the composite material. Unlike simple physical mixing, the composite material of the present invention has the advantages of an adjustable electric potential plateau, high reversible capacity, good cycle stability, power consumption early warning and the like.

Abstract: A polylactic acid triblock copolymer and a preparation method thereof are described. The polylactic acid triblock copolymer comprises an aromatic polyester oligomer block and a polylactic acid block. The polylactic acid triblock copolymer is obtained by reacting an aromatic polyester oligomer with a monomer lactide at a desired temperature. The polylactic acid block copolymer has a regular structure indicated by peak melting temperatures (Tm) corresponding to the aromatic polyester oligomer block and the polylactic acid block, respectively. Examples of the aromatic polyester oligomer block include polyethylene terephthalate, polybutylene terephthalate, and polyethylene 1,4-naphthalate. Examples of the monomer lactide include L-lactide and D-lactide.

Abstract: The present invention provides a method for preparing graphene, including reacting graphite in an acid solution in which an oxidant is present so as to obtain a graphene. Compared with the prior art, the advantages of the present invention reside in that, the graphene prepared by the method of the present invention has excellent quality and substantially increased yield and production rate, as compared with mechanical stripping, epitaxial growth, and chemical vapor deposition; and the graphene prepared by the method of the present invention has significantly improved quality, substantially reduced structural defects, and significantly increased conductivity, as compared with oxidation-reduction preparation in the solution-phase; besides, the method is also advantageous for a simple process, mild conditions, low cost, and very easy for scale production.