The present application relates to a method for liquid phase oxidation of durene, which comprises: a first stage, in the presence of a catalyst, with acetic acid as a solvent, a liquid phase oxidation reaction of an oxidant source and durene to produce an intermediate mixture, the catalyst containing Co salt, Mn salt, Zr salt and bromide compound; a second stage, adding a mixture of bromide and pure water to the intermediate mixture, and continuing the oxidation reaction with the oxidant source to produce pyromellitic acid; wherein the concentration of oxidant in the oxidant source of the first stage is lower than the concentration of oxidant in the oxidant source of the second stage. By controlling the concentration of oxidant in the oxidant source of the first stage to be lower than the concentration of oxidant in the oxidant source of the second stage in the liquid phaseoxidation process of durene, the yield of pyromellitic acid and the purity of crude pyromellitic acid are significantly improved.
The application belongs to the field of organic photovoltaics, and relates to a kind of polymer photovoltaic material and its preparation method and application. Double bromidecompound A and double side tin compound B are subjected to Stille cross coupling reaction under the action of palladium catalyst, and the polymer photovoltaic material is obtained. The polymer photovoltaic material prepared by the application has an ultra-wide absorption spectrum range from 300 nm to 1200 nm. Such material exhibits an ultra-wide spectral range and a high extinction coefficient, and embodies excellent light absorption capacity. The strong light absorption capacity of the polymer photovoltaic material prepared by the application will help to improve the device efficiency of organic photovoltaics and improve the energy conversion efficiency of the device. The polymer photovoltaic material prepared by the application provides reference value for the design of functional materials in many fields of organic photoelectricity and solar energy utilization and conversion.
This invention discloses a high color rendering index (Ra) and long lifespan magnetic ring-coupled plasmalight source and its preparation method. The light source is an electrodeless source, comprising a bulb shell, an inorganic ceramic protective layer, a luminescent filler encapsulated inside the bulb shell, a mixed buffer gas, and a magnetic ring coupler fitted outside the bulb shell. The luminescent filler contains sulfur (S), selenium (Se), rare earth triiodine compounds, alkali metalbromine compounds, and alkali metaliodine compounds. The mixed buffer gas is a mixture of argon (Ar) and krypton (Kr) or argon (Ar) and xenon (Xe). The preparation method includes five steps: bulb shell pretreatment, inorganic ceramic protective layer preparation, luminescent filler filling, vacuuming and gas filling, and fusion sealing. This invention achieves ultra-high color rendering indexes (Ra>95, R9>90) by optimizing the luminescent formula and structural design. It contains no toxic substances and meets environmental standards, solving the technical pain points of poor color rendering, short lifespan, and insufficient environmental friendliness of traditional plasma light sources.
This invention provides a catalyst for the liquid-phase oxidation of terephthalic acid and its application. The catalyst comprises a cobalt salt, a zirconium salt, a bromine-containing compound, and an auxiliary agent; the mass ratio of Co, Zr, Br, and the auxiliary agent in the catalyst is 500:(250–350):(500–1200):(30–80); the auxiliary agent is selected from compounds with the structure shown in formula (1), wherein R is selected from C1–C4 alkyl groups. The catalyst for the liquid-phase oxidation of terephthalic acid provided by this invention has a low Br content and good catalytic performance; its application in the liquid-phase oxidation of p-xylene to terephthalic acid can reduce the impurity content in the product and effectively improve the product yield.
This invention belongs to the field of membrane material technology and discloses a high-flux, acid-resistant polyquaternary ammoniumnanofiltration membrane and its preparation method. The method includes: (1) coating an aqueous solution containing cyclic tertiarynitrogen oligomers onto a porous support substrate membrane, wetting it, and then removing excess liquid; (2) subsequently coating the surface of the material obtained in step (1) with a hexane solution containing benzyl bromide, wetting it so that the tertiarynitrogen atoms on the cyclic tertiarynitrogen oligomers undergo a quaternization reaction with the benzyl bromide, gradually forming a dense separation membrane at the water-hexane interface; after the reaction is completed, it is dried to obtain the nanofiltration membrane. The nanofiltration membrane prepared by this invention overcomes the disadvantages of traditional polyquaternary ammonium membranes, which require several hours to prepare and have low permeability. A defect-free nanofiltration separation membrane can be prepared in just 1 minute. After soaking in 1M sulfuric acid for 30 days, it can still maintain high permeability and rejection rate, showing good application prospects.
The application discloses a kind of waste old containing bromineflame-retardant foamed polystyrene high-efficiency separation, harmless digestion and recovery method, innovatively using high-efficiency extraction technology, and the fat bromineflame retardant is separated with polystyrene material with high efficiency, and then respectively through polymerrecoverygranulation, strong base debromination under phase transfer catalysis and bromine extraction technology, realize polystyrene material and bromine resource complete recovery and recycling.The application can realize 100% complete recovery of polystyrene material and bromine resource, the removal rate of fat bromine compound is greater than 99.9%, and the whole recovery process does not produce harmful waste, with green sustainable development concept.