Abstract: A tire anti-tarnish protective solution and a preparation method thereof are provided. The preparation method includes: mixing 15 to 25 parts of a waterborne epoxy resin, 20 to 35 parts of a toughening waterborne resin, 0.5 to 2.5 parts of a modifier, 1 to 2 parts of a reactive ultraviolet (UV) absorber, 1 to 3.5 parts of an active agent, 2.6 to 5.5 parts of a film-forming additive and other additives, 0 to 6 parts of a pigment/filler, 0.05 to 0.2 part of a bactericide, and 40 to 60 parts of deionized water, adding 0.4 to 1.6 parts of a curing additive, 0.05 to 0.5 part of a stabilizer, and 0.1 to 0.8 part of a thickener under stirring, stirring a resulting mixture for a specified time, and filtering a resulting system to obtain the protective solution.

Abstract: Disclosed is a method for preparing a carbon material, comprising applying a voltage to an electrically conductive medium to form an electrically conductive path in an oxygen-free environment containing a carbon source and a catalyst to obtain the carbon material, wherein the electrically conductive medium includes a solid substrate or a liquid-phase electrically conductive system; under the condition that the electrically conductive medium is the liquid-phase electrically conductive system, the carbon material is obtained in the liquid-phase electrically conductive system; and under the condition that the electrically conductive medium is the solid substrate, the carbon material is obtained on a surface of the solid substrate.

Abstract: A process and a device for continuous flow side-chain alkylation which relate to the technical field of organic synthesis. In this process and the device for continuous flow side-chain alkylation, an ibuprofen raw material is prepared with alkylbenzene as a raw material. This raw material alkylbenzene is easily available and has a low cost, and is suitable for scale-up production. Moreover, an entire preparation process adopts continuous chemical synthesis, and a reaction time of each stage can be precisely controlled, which is beneficial to control a total reaction time and reduce an amount of impurities produced. In this way, a purity and a yield of the ibuprofen raw material are improved. In summary, a continuous synthesis method for side-chain alkylation of alkylbenzene provided by the present disclosure shows a low cost and a high yield.

Abstract: The present disclosure belongs to the technical field of chemical separation and purification, and in particular relates to a purification method and device for continuous distillation and separation of an ibuprofen intermediate raw material. The purification method comprises the following steps: carrying out a primary distillation on synthetic liquid to obtain a primary material and recovered 4-methyl-1-pentene, then carrying out a second-stage distillation on the primary material to obtain a second-stage material and a recovered crude toluene product; and carrying out a third-stage distillation on the second-stage material to obtain isobutyl benzene and a recovered crude n-butylbenzene product. Embodiment results show that the purification method provided by the present disclosure is high in product recovery rate and high in product purity, the purity of isobutyl benzene is up to 99.99 wt %, the recovery rate is up to 99.9 wt %, the impurity content is not higher than 50 ppm.

Abstract: The present disclosure provides an active zinc-based catalyst and a preparation method thereof, and use in catalyzing a rearrangement reaction of ibuprofen. The active zinc-based catalyst includes a carbon-based fiber material and nano-zinc oxide supported on a fiber surface of the carbon-based fiber material. The active zinc-based catalyst is introduced with the carbon-based fiber material, and the carbon-based fiber material is capable of increasing a specific surface area of the catalyst, thereby improving a dispersion degree of zinc oxide, increasing the number of catalytic active sites, and significantly improving a catalytic activity. Meanwhile, due to a certain mechanical strength, the carbon-based fiber material is capable of improving a mechanical strength of the catalyst, making the catalyst exist stably in ketal fluid, maintaining a stable morphology of the catalyst, and avoiding or inhibiting reduction of the catalytic active sites, thereby ensuring a catalytic stability.

Abstract: The present disclosure belongs to the technical field of chemical separation and purification, and in particular relates to a purification method and device for continuous distillation and separation of an ibuprofen intermediate raw material. The purification method comprises the following steps: carrying out a primary distillation on synthetic liquid to obtain a primary material and recovered 4-methyl-1-pentene, then carrying out a second-stage distillation on the primary material to obtain a second-stage material and a recovered crude toluene product; and carrying out a third-stage distillation on the second-stage material to obtain isobutyl benzene and a recovered crude n-butylbenzene product. Embodiment results show that the purification method provided by the present disclosure is high in product recovery rate and high in product purity, the purity of isobutyl benzene is up to 99.99 wt %, the recovery rate is up to 99.9 wt %, the impurity content is not higher than 50 ppm.

Abstract: A system for a deep-sea planktonic microorganism in-situ concentration, temperature maintaining and pressure maintaining sampling is provided and includes a sampling cylinder body with double layer structures, the sampling cylinder body is provided with a plug-shaped inner cavity, the plug-shaped inner cavity is provided with a transfer water outlet and a water inlet connected to a water inlet component, the plug-shaped inner cavity is connected to an end cover, the plug-shaped inner cavity is connected to a filter part, the sampling cylinder body is provided with a sampling water outlet, the sampling water outlet is respectively connected to a pressure maintaining device and a water outlet pipe, a temperature maintaining material layer and a temperature control component are connected between the double layer structures, and the temperature control component is electrically connected to a controller. The system can complete sampling on the premise of maintaining in-situ pressure of samples.

Abstract: The present disclosure provides an active zinc-based catalyst and a preparation method thereof, and use in catalyzing a rearrangement reaction of ibuprofen. The active zinc-based catalyst includes a carbon-based fiber material and nano-zinc oxide supported on a fiber surface of the carbon-based fiber material. The active zinc-based catalyst is introduced with the carbon-based fiber material, and the carbon-based fiber material is capable of increasing a specific surface area of the catalyst, thereby improving a dispersion degree of zinc oxide, increasing the number of catalytic active sites, and significantly improving a catalytic activity. Meanwhile, due to a certain mechanical strength, the carbon-based fiber material is capable of improving a mechanical strength of the catalyst, making the catalyst exist stably in ketal fluid, maintaining a stable morphology of the catalyst, and avoiding or inhibiting reduction of the catalytic active sites, thereby ensuring a catalytic stability.

Abstract: The present disclosure belongs to the field of energy materials, and relates to a preparation method of a solid electrolyte, in particular to a method for forming a membrane by using an electrolyte to activate a porous powder material prepared by in-situ polymerization of a polymer on the surfaces of cellulose nanocrystals, and then hot-pressing. According to the technical solution of the present disclosure, cellulose nanocrystals are used as templates, the powder material with a porous structure is prepared by in-situ polymerization growth of the polymer on the surfaces of the cellulose nanocrystals, a small amount of electrolyte is used to activate the powder, and the solid electrolyte is prepared by hot-pressing membrane formation. The solid electrolyte prepared by the present disclosure has excellent electrochemical performance and mechanical performance, and a broad application prospect.

Abstract: Disclosed is a system and a method for electrospinning superfine fiber bundling, belonging to the technical field of artificial fiber manufacturing, and comprises a spinning nozzle and a bundling disk which are coaxially arranged; the spinning nozzle is arranged at an upper part of the bundling disk; the bundling disk is connected with a motor through a coupling; the motor rotates to drive the bundling disk to rotate; a guide groove is also arranged outside the bundling disk; a center of the bundling disk is provided with a shaft; the insulated outer ring, the central conductive ring, the insulated inner ring and the shaft are fixed by bonding or thermal compounding; inner and outer edges of the central conductive ring are smooth circular arc rounded corners; an inner edge of the insulated outer ring and an outer edge of the insulated inner ring are corresponding smooth rounded corners.

Abstract: The present invention relates to a printing device and a printing method. The combination mode between materials in an additive manufacturing process is improved. A calculation unit is used for controlling an A pole unit and a B pole unit to be in contact with, the materials, to form an energized circuit. The surface temperature of phase change material in the material between the A pole unit and the B pole unit is greater than or equal to a preset temperature so that the materials at a distance can be simultaneously combined.

Abstract: The present disclosure belongs to the field of energy materials, and relates to a preparation method of a solid electrolyte, in particular to a method for forming a membrane by using an electrolyte to activate a porous powder material prepared by in-situ polymerization of a polymer on the surfaces of cellulose nanocrystals, and then hot-pressing. According to the technical solution of the present disclosure, cellulose nanocrystals are used as templates, the powder material with a porous structure is prepared by in-situ polymerization growth of the polymer on the surfaces of the cellulose nanocrystals, a small amount of electrolyte is used to activate the powder, and the solid electrolyte is prepared by hot-pressing membrane formation. The solid electrolyte prepared by the present disclosure has excellent electrochemical performance and mechanical performance, and a broad application prospect.

Abstract: An online measurement device for crystal size and shape in a high-solid-content crystallization process includes a solution amplifier, a measurement device, a peristaltic pump, a crystallization kettle, a dilution device and a solution storage tank. A crystal-containing solution is arranged in the crystallization kettle; an inner wall of the solution amplifier is smooth, one end is an amplification end, and the other end is a contraction end. The contraction end is communicated with one end of the solution storage tank and one end of the crystallization kettle. The amplification end is communicated with the dilution device and the peristaltic pump. The peristaltic pump is communicated with the other end of the crystallization kettle. The solution amplifier, the peristaltic pump and the crystallization kettle form a complete passage through a pipeline. A measurement instrument of the measurement device is arranged at the outer side of the solution amplifier.

Abstract: A measuring device for pore throat pressure of Jamin effect based on mechanochromic materials is provided and includes: a bubble pressurization part, configured to inject bubbles into a microscopic visualization test part; the microscopic visualization test part including a mechanochromic material and a pore throat structure, configured to characterize changes of pore throat pressure during bubble injection; a waste liquid recycling part, configured to recycle bubble waste liquid passing through the microscopic visualization test part; a data acquisition and analysis part, configured to acquire changing data of the pore throat pressure in the microscopic visualization test part and analyze the changing data to obtain the pore throat pressure. The device is simple in structure and easy to operate, and provides a method for measuring an internal surface pressure of an object. The method can realize a real time measurement of the pore throat pressure of Jamin effect.

Abstract: The present invention discloses a saline glycerine wastewater treatment system and technology. The whole technological process mainly includes a reaction process, an evaporation process, a crystallization process, a filtration process and a drying process. The present invention first proposes the use of an “ammonia-alkali reaction principle” to treat high-salt glycerine wastewater, which mainly solves the problem of treating a large amount of calcium chloride-containing glycerine wastewater produced in the production process of propylene oxide and epichlorohydrin in chlor-alkali industry, and places emphasis on solving the problems that low value-added calcium chloride produced in the wastewater treatment process of a traditional method has low quality, is basically accumulated as solid waste and is difficult to treat, and chloride ions have adverse effects on the biochemical process of wastewater treatment.

Abstract: The present disclosure is related to the field of polymer materials, and, in particular, to a method for synthesizing a bio-based polyamide. More specifically, the disclosure provides a method for synthesizing a block copolymer consisting of a hard segment of a polyamide prepared via solid state polycondensation and a soft segment of a polyether polyol. Due to a reaction of itaconic acid, which contains a carbon-carbon double bond, with hexamethylenediamine, the bio-based polyamide is greatly different from conventional linear polyamides and exhibits a lower glass transition temperature and excellent mechanical properties. Unlike conventional processes for preparing modified polyamides, the bio-based polyamide is synthesized, according to the method, through chain extension of a polyamide with an excess amount of a diisocyanate based on amine value of the polyamide and then crosslinking of the resulting product with a polyether polyol by using glycerol as a crosslinking agent.

Abstract: This application provides an intelligent robot for cleaning and mending a net cage and a method of using the intelligent robot, including: a control system, a main body, an attraction module, a motion module, a cleaning module and a mending module. The main body includes a streamlined pressure casing, and a drive mechanism and a water ballast tank which are located in the pressure casing. The attraction module includes electromagnets which are symmetrically provided at a bottom of the pressure casing. The motion module includes first and second motion mechanisms which are symmetrically provided at opposite sides of the pressure casing. A traveling path of the first motion mechanisms is perpendicular to a traveling path of the second motion mechanisms. The intelligent robot achieves cleaning and mending for both sides of the net cage, and is simple to operate, safe, high-efficient, economical and convenient.

Abstract: Provided are a phosphazene compound, a method for preparing a phosphazene compound and a method for producing a polymer with a phosphazene compound as a catalyst. The compound of formula (I) or a solvate thereof, where A is a six- or eight-membered ring consisting of repeated P?N, and B is at least one of unsubstituted or substituted C1-6 alkylamino, unsubstituted or substituted C1-6 cycloalkylamino, unsubstituted or substituted arylamino, or halogen, and B is attached to A at phosphorus in P?N, where R is unsubstituted or substituted C1-6 alkyl, unsubstituted or substituted C1-6 cycloalkyl, unsubstituted or substituted aryl, or unsubstituted or substituted benzyl, or R forms C1-6 heterocycloalkyl together with N attached thereto.

Abstract: A method for industrial production of a butadiene-isoprene copolymer rubber having a trans-1,4-structure (TBIR) and an apparatus for implementing the method. The production method includes: pumping a predetermined amount of a butadiene and an isoprene into a polymerization reactor, and performing bulk polymerization in the presence of a catalyst to obtain TBIR; performing extrusion, devolatilization, granulation and drying on the produced TBIR, and then packaging the produced TBIR; and separating unreacted monomers by a recovery and separation device followed by separately refining the unreacted monomers, and then returning the unreacted monomers to a batching device or a storage tank. The production apparatus has a recovery and refining unit, a polymerization unit, a post-treatment unit and a utility unit. By the production apparatus and the production method industrial production of TBIR by bulk polymerization is realized.

Abstract: A gas-assisted rubber wet mixing preparation apparatus is disclosed, including a rack, a reactor is fixedly mounted below the rack; a mixing chamber in an ellipsoidal shape is provided inside the reactor; the reactor is provided with a plurality of feed ports, the feed ports are provided at an included angle with respect to the horizontal plane; spray guns cooperating with the feed ports are fixedly mounted on an outer wall of the reactor, a material storage tank and a gas supply device are connected to the spray gun; the spray guns and the material storage tanks are in one-to-one correspondence, and the spray guns are connected to the corresponding material storage tanks respectively; a discharge port is further provided below the reactor, and a receiver tray is provided below the discharge port.