Abstract: The present disclosure discloses a method for realizing macroscopic super-lubrication by a matching pair of nano metal-coated steel balls and hydrogen-containing carbon films, which is based on the use of nano metal-coated steel balls and diamond-like films with a hydrogen content of 25-30% as the matching pair. Further, a tribochemical reaction occurs through the catalytic action of nano metal during the friction process to form a nano graphene transfer film with incommensurate contact at the contact interface to achieve macroscopic super-lubrication.

Abstract: The present invention discloses a phthalide derivative, the structure of said derivative is represented by Formula (I) or Formula (II). The present invention also discloses the preparation method and use of said derivative. The phthalide compound obtained through structure modifications in the present invention enhances the chemical stability and pharmacological activity of the phthalide compound, facilitating the improvement of the druggability of such compounds.

Abstract: A hydrogen-free carbon film polymer lubricating material and a preparation method and use thereof are disclosed. In the method, a graphite target is used as the target material, and a magnetron sputtering deposition is performed on a surface of the polymer substrate, thereby physically depositing and forming a hydrogen-free carbon film on the surface of the polymer substrate, thereby obtaining a hydrogen-free carbon film polymer lubricating material.

Abstract: The disclosure relates to a method for mechanochemical preparation of an iron red pigment, which comprise steps: mixing a clay mineral, a soluble iron source and an alkali source in a mill for grinding to obtain a precursor, wherein the ratio of ball to material is controlled at 20-50, the grinding speed is 300-1200 rpm, and the grinding time is 30-360 min; and calcining the precursor at 500-900° C. for 30-120 min to obtain a high-performance iron oxide red/clay mineral hybrid pigment. The iron oxide red/clay mineral hybrid pigment has a bright and beautiful color, high-temperature and acid resistance, and can satisfy requirements for high-performance iron oxide red pigments in fields of paints, inks, ceramics, anti-corrosive coatings, etc. Furthermore the method is a simple process without waste that is environmentally friendly and suitable for industrialized production, thus it is expected to replace existing processes of iron oxide red pigments.

Abstract: The present disclosure discloses a preparation method of a multi-functional marine engineering alloy. Through the coupling of a multi-principal alloy structure, structural entropy, and temperature and powder metallurgy and heat treatment, mutual solubility between elements and free energy of an alloy system are regulated, Cu grain boundary segregation is eliminated, and uniform and dispersed nano-precipitation of the anti-fouling element Cu in corrosion-resistant and high-plasticity multi-principal alloys is realized. The preparation method is simple and controllable to operate, and the prepared material has plasticity higher than 75%, high yield strength, excellent corrosion resistance and anti-fouling property, and has important application prospects in the field of marine engineering.

Abstract: Disclosed is a method for preparing an attapulgite-based pH-responsive antibacterial material, including: directly spraying a natural aldehyde-based antibacterial agent onto an attapulgite powder under stirring, and constantly stirring the attapulgite powder for 20-30 min; grinding the attapulgite powder in a ball mill for 30-60 min to obtain a ground attapulgite powder; placing the ground attapulgite powder in a stirred tank, and spraying a chitosan-citric acid aqueous solution onto the ground attapulgite powder; after spraying, constantly stirring the ground attapulgite powder for 30-120 min; and finally drying the ground attapulgite powder to obtain a dried attapulgite powder, sieving the dried attapulgite powder to obtain a sieved attapulgite powder, and packaging the sieved attapulgite powder to obtain the antibacterial material.

Abstract: The present disclosure provides a method for modifying a hydrogel lubricating coating on a surface of general equipment, and hydrogel lubricating coating-modified general equipment, belonging to the technical field of material surface modification. In the present disclosure, by combining catechol adhesion chemistry and free radical polymerization initiated by surface catalysis, the method can realize in-situ generation of free radicals at an interface of a substrate and a hydrogel monomer solution at room temperature, without external auxiliary conditions such as illumination or heating. The method can prepare the hydrophilic hydrogel lubricating coating on the surface of almost all existing substrates, which is especially suitable for lubricating modification on an inner surface of a non-translucent pipeline instrument, showing material versatility. Therefore, the method is suitable for the fields of surface engineering and biomedicine.

Abstract: A method for preparing an ammonium thiomolybdate-porous amorphous carbon composite superlubricity film is disclosed. First, a porous amorphous carbon film is prepared by an anode layer ion source assisted plasma chemical vapor deposition method and a reactive magnetron sputtering method on a substrate. The porous amorphous carbon film is then impregnated in an ammonium thiomolybdate solution, so that the ammonium thiomolybdate is adsorbed on the porous amorphous carbon film, and the impregnated porous amorphous carbon film is air dried.

Abstract: The present disclosure discloses a preparation method of a multi-functional marine engineering alloy. Through the coupling of a multi-principal alloy structure, structural entropy, and temperature and powder metallurgy and heat treatment, mutual solubility between elements and free energy of an alloy system are regulated, Cu grain boundary segregation is eliminated, and uniform and dispersed nano-precipitation of the anti-fouling element Cu in corrosion-resistant and high-plasticity multi-principal alloys is realized. The preparation method is simple and controllable to operate, and the prepared material has plasticity higher than 75%, high yield strength, excellent corrosion resistance and anti-fouling property, and has important application prospects in the field of marine engineering.

Abstract: Disclosed is an oil-containing fiber-polymer self-lubricating composite material. The composite material includes a resin matrix and an oil-containing fiber dispersed in the resin matrix, wherein a mass ratio of the resin matrix to the oil-containing fiber is in the range of 100:(1-10); the resin matrix is a photocurable resin or a thermosetting resin; the oil-containing fiber comprises a natural fiber and a lubricating oil adsorbed in the natural fiber.

Abstract: The present invention provides a waterborne self-polishing antifouling paint and a preparation method and application thereof, and belongs to the technical field of marine antifouling paints. The waterborne self-polishing antifouling paint provided by the present invention includes the following components in parts by weight: 30-60 parts of waterborne self-polishing emulsion, 30-70 parts of waterborne slurry, 0.1-0.5 parts of waterborne leveling agent, 0.2-1 parts of waterborne defoamer, 0.5-1 parts of film-forming additive and 10-20 parts of water. The waterborne self-polishing antifouling paint provided by the present invention has an ultra-low content of volatile organic compounds (VOCs) (less than 20 g/L), and is environmentally friendly. The waterborne self-polishing antifouling paint can be formed into a paint film with good mechanical properties, stable self-polishing rate, and excellent water immersion resistance and antifouling performance.

Abstract: A boron-nitrogen ligand with a chiral 1,2-ethylenediamine backbone, a preparing method and used thereof are provided. The structural formula of the boron-nitrogen ligand is as shown in formula (I): wherein R1, R2 and R3 are respectively at least independently selected from substituted or unsubstituted C3-C10 cycloalkyl, C1-C10 alkyl or aryl; R4, R5, R6, R7, R8, R9, R10, R11 and R12 are respectively at least independently selected from hydrogen, halogen, substituted or unsubstituted C1-C10 alkyl, C1-C4 alkoxy, C3-C30 cycloalkyl or aryl; Ar1 and Ar2 are respectively at least independently selected from substituted or unsubstituted C6-C30 aryl. The preparation method of the present application is simple, and can be used for preparing a racemic or chiral boron-nitrogen ligand, which can be used as a catalyst for an asymmetric catalytic reaction and has economic practicability and industrial application prospects.

Abstract: The present invention discloses a phthalide derivative, the structure of said derivative is represented by Formula (I) or Formula (II). The present invention also discloses the preparation method and use of said derivative. The phthalide compound obtained through structure modifications in the present invention enhances the chemical stability and pharmacological activity of the phthalide compound, facilitating the improvement of the druggability of such compounds.

Abstract: A boron-nitrogen ligand with a chiral 1,2-ethylenediamine backbone, a preparing method and used thereof are provided. The structural formula of the boron-nitrogen ligand is as shown in formula (I): wherein R1, R2 and R3 are respectively at least independently selected from substituted or unsubstituted C3-C10 cycloalkyl, C1-C10 alkyl or aryl; R4, R5, R6, R7, R8, R9, R10, R11 and R12 are respectively at least independently selected from hydrogen, halogen, substituted or unsubstituted C1-C10 alkyl, C1-C4 alkoxy, C3-C30 cycloalkyl or aryl; Ar1 and Ar2 are respectively at least independently selected from substituted or unsubstituted C6-C30 aryl. The preparation method of the present application is simple, and can be used for preparing a racemic or chiral boron-nitrogen ligand, which can be used as a catalyst for an asymmetric catalytic reaction and has economic practicability and industrial application prospects.

Abstract: The present invention relates to the field of 3D printing technology, and provides a photocurable 3D printing polyimide ink, and a preparation method and application thereof. The photocurable 3D printing polyimide ink includes the following components in the following weight percentages: 40 to 60% of a photocurable polyamic acid, 5 to 40% of an organic solvent, 10 to 50% of a reactive diluent, 1 to 10% of a chain extender, and 1 to 3% of a photoinitiator. The photocurable 3D printing polyimide ink provided by the present invention has excellent mechanical properties, thermal stability, relatively high printing accuracy and relatively low shrinkage; a molded device obtained by 3D printing has excellent properties including high accuracy, great dimensional stability, high strength and corrosion resistance, excellent flexibility, high temperature resistance and relatively low shrinkage. The method for preparing the photocurable 3D printing polyimide ink has a simple process and lower energy consumption.

Abstract: A method for preparing a direct-writing polyimide additive manufacturing (AM) material includes (1) conducting ultraviolet curing immediately after the photosensitive polyimide ink is subjected to direct-writing extrusion, to obtain a polyimide precursor formed member; and (2) heat-treating the polyimide precursor formed member obtained in step (1) to obtain the direct-writing polyimide AM material. The direct-writing polyimide AM material obtained by using the method of the present invention has excellent comprehensive properties.

Abstract: The present invention provides a waterborne self-polishing antifouling paint and a preparation method and application thereof, and belongs to the technical field of marine antifouling paints. The waterborne self-polishing antifouling paint provided by the present invention includes the following components in parts by weight: 30-60 parts of waterborne self-polishing emulsion, 30-70 parts of waterborne slurry, 0.1-0.5 parts of waterborne leveling agent, 0.2-1 parts of waterborne defoamer, 0.5-1 parts of film-forming additive and 10-20 parts of water. The waterborne self-polishing antifouling paint provided by the present invention has an ultra-low content of volatile organic compounds (VOCs) (less than 20 g/L), and is environmentally friendly. The waterborne self-polishing antifouling paint can be formed into a paint film with good mechanical properties, stable self-polishing rate, and excellent water immersion resistance and antifouling performance.

Abstract: Provided is a process for the production of an aromatic compound comprising at least two amine functions, comprising reacting an aromatic compound having at least one hydroxyl function and at least one aldehyde function with a second reactant having an amine function, in the presence of a reductant agent and a catalyst comprising at least one metal element in elemental form and/or at least one metal oxide.

Abstract: A derivative of isocorydine of formula I: wherein: R1? X?N, C, C?C; n1=0, 1 R2?H, R1 Y?C, N R3?H, Cl, Br, F, CF3, OCH3, CH3, Z ?H, Cl, F, N; n2=0, 1 R4?NH2, CH2NH2, NHCO(CH2)n3CH3, CH2NHCO(CH2)n3CH3, n3=0, 1, 2. This derivative is prepared by amidation condensation reaction between an amino group of NICD and a carbonyl group of an aryl isocyanate, a carboxylic acid, or an acid chloride, or symmetrical amidation condensation reaction between an NICD and an aromatic amino group by solid phosgene. This derivative has anti-cancer activity in vivo and in vitro, and may be used for preventing and treating cancer.

Abstract: The present invention discloses a method for preparing a double-network hydrogel tube with a complex structure. Iron wires of different sizes are mechanically polished, arranged in different manners, and then immersed into a monomer prepolymer solution, or a monomer prepolymer is poured into a container containing iron wires of different arranged shapes to conduct a polymerization reaction, such that a uniform primary-crosslinked single-network hydrogel film can be rapidly grown on the surface of each iron wire. The hydrogel film is then immersed in a secondary-crosslinking solution for secondary crosslinking to build a double-network hydrogel film. After immersion processing, the wires are drawn out to obtain high-strength hollow double-network hydrogel tubes of different shapes. The hydrogel tube has a diameter of 10 micrometers to a few millimeters, the shape of the tube inner structure is highly controllable, and the tensile strength of the hydrogel tube can be up to 2 MPa.