Abstract: The invention provides a light spot scanning device, a scanning method thereof, and a medical cosmetology device, belonging to the technical field of medical cosmetology, comprising a laser and a collimating lens and a reflector arranged in sequence along the optical path transmission direction of the laser. The reflector is also connected with a driving member, the laser beam emitted by the laser forms a linear light spot through the collimating lens, and the reflector is driven to continuously rotate according to a preset path through the driving member. A plurality of linear light spots formed by the continuous rotation are sequentially overlapped on the light exiting side of the reflector to form a scanning linear light spot. Each time the reflector rotates, a group of linear light spots is formed. After continuous rotation, multiple groups of sequentially overlapping linear light spots are formed on the light exiting side of the reflector, called scanning linear light spots.

Abstract: A method of forming an electrode material includes: (1) loading an electrochemically active material onto graphene sheets; (2) combining the electrochemically active material-loaded graphene sheets with holey graphene oxide sheets to form a mixture; and (3) treating the mixture under reducing conditions to form a composite including a graphene framework loaded with the electrochemically active material.

Abstract: A device for simulating high-frequency current propagation of partial discharge of a GIL/GIS is disclosed. The device comprises a casing, a busbar cavity, an adjustable impedor, a first metal support, a second metal support, a third metal support, and a high-frequency current sensor. The first metal support and the second metal support are separated by an insulating support, the third metal support has an end connected to the second metal support, as well as an end connected to a grounding grid, and the adjustable impedor is formed by an adjustable resistor and an adjustable inductor which are connected in series, and is connected in series between the first metal support and the second metal support through a wire.

Abstract: Disclosed are an amide compound having iodoaryl or iodoheteroaryl, a preparation method therefor and a use thereof. The amide compound having iodoaryl or iodoheteroaryl can be used to prepare an X-ray imaging embolic material with improved imaging modification efficiency, thus increasing the iodine content of the X-ray imaging embolic material.

Abstract: A power supply apparatus includes: a housing provided with at least one air inlet hole and a noise reduction cavity; and a plurality of micropores enabling the at least one air inlet hole to communicate with the noise reduction cavity, the plurality of micropores being formed inside the housing. In an embodiment, a diameter of each micropore of the plurality of micropores ranges from 0.3 to 1 mm.

Abstract: A vaporizer is disclosed. The vaporizer includes a liquid storage housing having a liquid storage cavity formed therein and a base arranged at one end of the liquid storage housing. The base includes an air inlet protruding stage that has an upper surface facing the liquid storage cavity. The upper surface is in a shape of a protrusion. The air inlet protruding stage is provided with a plurality of air inlet holes extending from the upper surface away from the liquid storage cavity.

Abstract: An absorbable iron-based instrument is provided having an iron-based substrate, a zinc-containing protector in contact with the iron-based substrate, and a degradable polyester in contact with the iron-based substrate and/or the zinc-containing protector. The range of the ratio of the mass of the zinc-containing protector to the mass of the iron-based substrate is 1:200 to 1:2. In the degradable polyester, the mass fraction of a low-molecular-weight part with a molecular weight of less than 10,000 is less than or equal to 5%; alternatively, in the degradable polyester, the mass fraction of a residual monomer is less than or equal to 2%.

Abstract: A method of forming an electrode material includes: (1) loading an electrochemically active material onto graphene sheets; (2) combining the electrochemically active material-loaded graphene sheets with holey graphene oxide sheets to form a mixture; and (3) treating the mixture under reducing conditions to form a composite including a graphene framework loaded with the electrochemically active material.

Abstract: A method of forming an electrode material includes: (1) loading an electrochemically active material onto graphene sheets; (2) combining the electrochemically active material-loaded graphene sheets with holey graphene oxide sheets to form a mixture; and (3) treating the mixture under reducing conditions to form a composite including a graphene framework loaded with the electrochemically active material.

Abstract: An absorbable iron-based device includes an iron-based matrix and degradable polyester in contact with the surface of the iron-based matrix. The mass fraction of a low-molecular-weight part of the degradable polyester is less than or equal to 5%, and the molecular weight of the low-molecular-weight part is less than 10,000; or the mass fraction of a residual monomer in the degradable polyester is less than or equal to 2%.

Abstract: An absorbable iron-based instrument is provided having an iron-based substrate, a zinc-containing protector in contact with the iron-based substrate, and a degradable polyester in contact with the iron-based substrate and/or the zinc-containing protector. The range of the ratio of the mass of the zinc-containing protector to the mass of the iron-based substrate is 1:200 to 1:2. In the degradable polyester, the mass fraction of a low-molecular-weight part with a molecular weight of less than 10,000 is less than or equal to 5%; alternatively, in the degradable polyester, the mass fraction of a residual monomer is less than or equal to 2%.

Abstract: An absorbable iron-based alloy implantable medical device includes an iron-based alloy matrix, a degradable polymer coating disposed on the surface of the iron-based alloy matrix, and a corrosion inhibition layer disposed on the surface of the iron-based alloy matrix. The corrosion inhibition layer can delay early-stage corrosion of the iron-based alloy matrix, ensure mechanical performance of a medical device in the early stage of the implantation, prevent degradation of a polymer in the early stage of the implantation of the medical device, and reduce the usage of the degradable polymer, thereby reducing risks of inflammatory reactions.

Abstract: Disclosed is an implanted device, comprising a device base body and an active drug, wherein the device base body is pure zinc and/or a zinc alloy, the zinc content in the device base body is 0.1-100%, and the active drug comprises anti-allergic drugs. After the implantation of the implanted device into the human body, the surrounding tissues of the implant would not have a clear hypersensitive reaction due to the presence of the anti-allergic drugs, and the implanted device can be used to be implanted into the body for supporting organ chambers, to fill the hollow chambers of the organs and tissues or as orthopaedic implants etc.

Abstract: An implantable medical instrument is made of an iron-based alloy, comprising an iron-based alloy substrate and a drug-loaded coating. The drug-loaded coating comprises a polymer and an active drug; the weight average molecular weight of the polymer is greater than or equal to 50,000 and less than or equal to 1,000,000; micro-pores having a diameter of less than or equal to 10 micrometers are formed in the drug-loaded coating; the percentage of the active drug released on the implantable medical instrument made of an iron-based alloy is greater than or equal to 4t1/2?1 and less than or equal to 6.9t1/2+63, wherein t ? (0, 28], and t represents sampling time/days.

Abstract: An implantable device including a matrix and a zinc-containing layer at least partially covering the substrate. The zinc-containing layer includes a zinc compound. The ratio of the mass of the zinc element in the zinc-containing layer to the surface area of the implantable device is 0.1-200 ?g/mm2. The average porosity of the zinc-containing layer is 30% or less. By matching the ratio of the mass of zinc in the zinc-containing layer to the surface area of the implantable device with the average porosity of the zinc-containing layer, the release rate of zinc is controlled within a reasonable range so that the rate of formation of the zinc-containing substance is controlled such that the concentration of the zinc-containing substance accumulated in the tissue is higher than the concentration which inhibits the proliferation of smooth muscle cells, and is always lower than the toxic concentration which causes cell death.

Abstract: An implantable apparatus, including at least one corrodible zinc-containing portion, where a content range of zinc in the at least one zinc-containing portion is [30, 50) wt. % and zinc in the zinc-containing portion is an amorphous structure, or a content range of zinc in the at least one zinc-containing portion is [50, 70] wt. %, and a microscopic structure of zinc in the zinc-containing portion is at least one of an amorphous structure, a non-equiaxed structure, an ultrafine-grained structure, or an equiaxed structure with a grain size number of 7 to 14, or a content range of zinc in the at least one zinc-containing portion is (70, 100] wt. % and a microscopic structure of zinc in the zinc-containing portion is at least one of a non-equiaxed structure, an ultrafine-grained structure, or an equiaxed structure with a grain size number of 7 to 14.

Abstract: A degradable iron-based alloy stent comprises an iron-based alloy substrate and a degradable polymer in contact with the surface of the substrate. The weight-average molecular weight of the degradable polymer is in the range of [1, 100]*104, and the polydispersity index of the degradable polymer is in the range of (1.0, 50]. The degradable polymer is selected from a degradable polyamino acid that can generate an acidic amino acid after degradation; or a mixture of the degradable polyamino acid and a degradable polyester, or a copolymer of monomers of the two; or a mixture of the degradable polyamino acid and a degradable polymer that does not generate acidic products after degradation, or a copolymer of the monomers of the two; or a mixture of the degradable polyamino acid, the degradable polyester and the degradable polymer that does not generate acidic products after degradation, or a copolymer of monomers of the three, or a mixture of a copolymer of monomers of any two of the three with the remaining one.

Abstract: A method of winding a flexible cable, a carrying equipment and a gimbal are provided. The method is used for electrical connection in the carrying equipment, and includes winding a multilayer flexible cable provided in layered stack on a carrier device to form a winding structure, and the winding structure includes at least one force offsetting unit including a first bending part and a second bending part bent in opposite directions.

Abstract: An electric motor, a gimbal and an unmanned aerial vehicle. The electric motor includes: a stator assembly; and a rotor assembly rotatably connected with the stator assembly. The stator assembly includes a stator housing for installation of a stator, the rotor assembly includes a rotor housing for installation of a rotor, and at least one of the stator housing and the rotor housing has a connecting arm. The gamble includes an electric motor group. At least one electric motor in the electric motor group is the above electric motor.

Abstract: An absorbable iron-based device includes an iron-based matrix and degradable polyester in contact with the surface of the iron-based matrix. The mass fraction of a low-molecular-weight part of the degradable polyester is less than or equal to 5%, and the molecular weight of the low-molecular-weight part is less than 10,000; or the mass fraction of a residual monomer in the degradable polyester is less than or equal to 2%.