Abstract: A structurally stable composite structural chromogenic material and a preparation method thereof are provided. The structurally stable composite structural chromogenic material is formed by stacking a transparent thermoplastic polymer and a structural chromogenic material layer by layer and then thermally bonding the peripheral edges of the polymer into a whole, and the upper surface layer and the lower surface layer of the material are both thermoplastic polymers. The molded composite structure has relatively obvious structural color and good mechanical strength.

Abstract: A double-inverse opal photonic crystal resin film is formed by embedding nanospheres in pores of polyacrylate inverse opal framework material and then filling the pores of the double-inverse opal photonic crystal resin film with an ethanol solution with hydrophilic acrylamide dissolved therein followed by photopolymerization to form a polyacrylamide network, so as to obtain the double-inverse opal photonic crystal resin film using water as ink. A mass fraction of hydrophilic acrylamide in the ethanol solution is 2 to 8 wt.%. The resin film can induce water to penetrate into the pores of the double-inverse opal photonic crystal resin film, making the nanospheres in the pores of the inverse opal framework distribute from random to order under the action of buoyancy force, thereby eliminating scattering interference and producing brilliant structural colors by regulating refractive index contrast.

Abstract: A structurally stable composite structural chromogenic material and a preparation method thereof are provided. The structurally stable composite structural chromogenic material is formed by stacking a transparent thermoplastic polymer and a structural chromogenic material layer by layer and then thermally bonding the peripheral edges of the polymer into a whole, and the upper surface layer and the lower surface layer of the material are both thermoplastic polymers. The molded composite structure has relatively obvious structural color and good mechanical strength.

Abstract: A bilayer photonic crystal photoswitch thin-film device having the optical characteristics of both 2D and 3D photonic crystals, and a preparation method thereof are provided. When the bilayer photonic crystal photoswitch thin-film device is rotated periodically, different colors can be observed at a fixed rotation angle, that is, the device has the attribute of changing colors by means of rotation, and can thus realize the opening and closing of an optical path. The bilayer photonic crystal photoswitch thin-film new device has broad application prospects in the fields of photoswitches, optical waveguides, optical prisms, warming signs, anti-counterfeiting and information coding, etc.

Abstract: The present invention relates to the technical field of new materials, and relates to a thermal conduction enhanced organic composite shape-stabilized phase change material and a preparation method thereof. A thermal conduction enhanced organic composite shape-stabilized phase change material, which is composed of a coordination crosslinked network polymer, an organic solid-liquid phase change material and a thermal conduction enhancer, the mass percent are as follows: coordination crosslinked network polymer 1-50%, organic solid-liquid phase change material 40-98.9%, and thermal conduction enhancer 0.1-10%, the coordination crosslinked network polymer being formed by complexing of polymer compound with metal ions. The invention has simple synthesis process and convenient applications, the material having large enthalpy of phase change, excellent shape stabilizing effect, while the phenomenon of liquid leakage will not occur during operation.

Abstract: Provided is a test paper kit for rapid graded quantitative detection of aromatic primary amine content in an acidic solution and an application thereof, and belongs to the field of detection. A test paper kit for rapid graded quantitative detection of aromatic primary amine content in an acidic solution, including 9 independent test paper sheets I-IX, wherein the test paper sheets are obtained by soaking filter paper in the following solutions respectively and then drying the filter paper: the test paper sheets I-III are soaked in alcoholic solutions of p-dimethylaminobenzaldehyde with three concentrations respectively; the test paper sheets IV-VI are soaked in alcoholic solutions of p-hydroxybenzaldehyde with three concentrations respectively, and the test paper sheets VII-IX are soaked in alcoholic solutions of p-methoxybenzaldehyde with three concentrations respectively.

Abstract: A composite material is applicable for photothermal energy conversion and thermal energy storage form-stable phase change. The composite material includes a supporting material and an organic phase-change material. The mass ratio of the supporting material to the organic phase change material is 3:7 to 1:9. The supporting material is lamellar, and the organic phase change material is evenly filled between supporting material layers to form a layered stacked structure. The supporting material is a nanosheet of Ti2C, Ti3C2, Ti3CN, V2C, Nb2C, TiNBC, Nb4C3, TA4C3, (Ti0.5Nb0.5)2C, or (V0.5Cr0.5)3C2. The organic phase-change material is paraffin, fatty acid, fatty acid ester or alcohol compound.

Abstract: The present invention relates to the technical field of new materials, and relates to a thermal conduction enhanced organic composite shape-stabilized phase change material and a preparation method thereof. A thermal conduction enhanced organic composite shape-stabilized phase change material, which is composed of a coordination crosslinked network polymer, an organic solid-liquid phase change material and a thermal conduction enhancer, the mass percent are as follows: coordination crosslinked network polymer 1-50%, organic solid-liquid phase change material 40-98.9%, and thermal conduction enhancer 0.1-10%, the coordination crosslinked network polymer being formed by complexing of polymer compound with metal ions. The invention has simple synthesis process and convenient applications, the material having large enthalpy of phase change, excellent shape stabilizing effect, while the phenomenon of liquid leakage will not occur during operation.

Abstract: Disclosed is a method for continuously preparing a water-soluble azo dye by coupling a nebulizer with a pipeline. According to the method, the nebulizer is coupled with a pipeline with an interception tower plate, atomized and mixed reaction liquid flow flows through the pipeline with the interception tower plate, and mixing and reacting are further enhanced through turbulent mixing on the tower plate, so that instant separation of reaction heat generated in an atomizing contact reaction from a reactant is achieved, and normal-temperature rapid continuous production of the water-soluble azo dye is achieved. Fog drops which are atomized by using the nebulizer have small particle diameter and large specific surface area, so that a diazo salt and a coupling component are sprayed separately, move face to face and can be fully contacted, and mixing and reacting speeds are increased.

Abstract: The present invention provides a group of water-soluble sulfur dye having carboxyl groups. For the kind of dye, a sulfur dye is first reduced to a leuco compound by sodium sulfide, and the leuco compound reacts with an active compound containing carboxyl groups to obtain a water-soluble sulfur dye containing the carboxyl group. The water-soluble sulfur dye provided by the present invention is applicable to dying of cotton, wool, silk, and leather. Being both water-soluble and carboxyl group reactive, the product has a simple application process and desirable color fastness, thereby having broad application prospects.

Abstract: The present invention provides a polycarboxylic acid dye with low polymerization degree, which is formed by using a macromolecule skeleton of polymaleic acid linked to an azo chromophore, an azo-metal complexation chromophore or an anthraquinone chromophore via a bridge group of amide or ester bond. The dye is useful for dyeing and printing leather, protein fiber, cellulose fiber and synthetic fiber.

Abstract: Disclosed is a method for continuously preparing a water-soluble azo dye by coupling a nebulizer with a pipeline. According to the method, the nebulizer is coupled with a pipeline with an interception tower plate, atomized and mixed reaction liquid flow flows through the pipeline with the interception tower plate, and mixing and reacting are further enhanced through turbulent mixing on the tower plate, so that instant separation of reaction heat generated in an atomizing contact reaction from a reactant is achieved, and normal-temperature rapid continuous production of the water-soluble azo dye is achieved. Fog drops which are atomized by using the nebulizer have small particle diameter and large specific surface area, so that a diazo salt and a coupling component are sprayed separately, move face to face and can be fully contacted, and mixing and reacting speeds are increased.

Abstract: The present invention provides a group of water-soluble sulfur dye having carboxyl groups. For the kind of dye, a sulfur dye is first reduced to a leuco compound by sodium sulfide, and the leuco compound reacts with an active compound containing carboxyl groups to obtain a water-soluble sulfur dye containing the carboxyl group. The water-soluble sulfur dye provided by the present invention is applicable to dying of cotton, wool, silk, and leather. Being both water-soluble and carboxyl group reactive, the product has a simple application process and desirable color fastness, thereby having broad application prospects.

Abstract: The present invention provides a polycarboxylic acid dye with low polymerization degree, which is formed by using a macromolecule skeleton of polymaleic acid linked to an azo chromophore, an azo-metal complexation chromophore or an anthraquinone chromophore via a bridge group of amide or ester bond. The dye is useful for dyeing and printing leather, protein fiber, cellulose fiber and synthetic fiber.