740 results about "Zinc salts" patented technology

The invention belongs to the technical field of pharmaceutical chemical processes, and particularly relates to a preparation method of a penem antibiotic intermediate 4-BMA, which comprises the following steps: adding Zn powder, chlorosilane, aliphatic tertiary amine, zinc salt and 4-AA in a formula (I) into THF (tetrahydrofuran), uniformly stirring, dropwise adding a THF solution of alpha-haloamide with an induction group in a formula (II) for reaction, filtering the reaction solution, removing the zinc powder, and drying to obtain the penem antibiotic intermediate 4-BMA. Extracting the filtrate to obtain a THF phase, washing with an aqueous solution of potassium oxalate, and recovering THF to obtain a formula (III); and carrying out oxidative hydrolysis, sulfur dioxide quenching, sulfur dioxide acid regulation crystallization and recrystallization on the formula (III) to obtain the intermediate 4-BMA. According to the preparation method disclosed by the invention, a zinc salt is used as a catalyst during preparation of the formula (III), potassium oxalate is used for removing residual Zn (II) in a THF phase, SO2 is used for quenching hydrogen peroxide and acid regulation and crystallization of 4-BMA, the oxygenolysis problem of 4-BMA is solved, and the preparation method has the characteristics of greenness, safety and high efficiency, is strong in product competitive advantage and is suitable for industrial production.

The invention relates to a composite hydroxypropyl methylcellulose skeleton sustained-release material and a preparation method thereof, and belongs to the technical field of drug sustained release. The sustained-release material is prepared from 70 to 90 parts of hydroxypropyl methylcellulose (HPMC), 10 to 20 parts of sodium alginate, 8 to 15 parts of chitosan, 0.1 to 0.2 part of Omega-3 fatty acid, 0.05 to 0.06 part of vitamin D, 2.5 to 5 parts of soluble calcium salt-zinc salt composite cross-linking agent, 0.5 to 1.5 parts of hydrolyzable cross-linking agent, 3 to 10 parts of enzyme sensitive auxiliary material, 1 to 5 parts of pore-foaming agent and 2 to 8 parts of hydrophobic blocking agent. The preparation method comprises the steps of raw material pretreatment and dry mixing, active component dispersion liquid preparation, wet granulation and primary cross-linking, secondary cross-linking and drying, vacuum drying and size stabilization, curing and packaging and the like. The sustained-release material provided by the invention has the advantages of controllable drug release rate, good mechanical strength and biodegradability, is suitable for sustained-release delivery of Omega-3 fatty acid, vitamin D and other active components, and can improve the bioavailability and stability of drugs.

The invention relates to the technical field of water-based energy storage batteries, in particular to a two-phase electrolyte for a water-based zinc ion battery and a preparation method of the two-phase electrolyte, and the two-phase electrolyte comprises soluble zinc salt, water and quaternary ammonium nitrate; the soluble zinc salt comprises one of zinc trifluoromethanesulfonate, zinc bis (trifluoromethylsulfonyl) imide, zinc acetate, zinc sulfate and zinc chloride, and the molar concentration of the soluble zinc salt is 1-5 mol / L; the quaternary ammonium nitrate is one or more than two of tetramethylammonium nitrate, tetraethyl ammonium nitrate, tetrabutyl ammonium nitrate, hexadecyl trimethyl ammonium nitrate and octadecyl trimethyl ammonium nitrate, and the molar concentration of the quaternary ammonium nitrate is 1-3 mol / L. The preparation method is simple, convenient and efficient, the reversibility of the zinc anode is optimized, the method is crucial for promoting the design of a practical water-based zinc ion battery, and the application of the zinc-based battery in the field of energy storage is further accelerated.

The application discloses a preparation method of a catalyst for liquid-phase refining of crude octanol, and the preparation method comprises the following steps: (1) mixing pretreated fly ash and pseudo-boehmite, adding deionized water and nitric acid, stirring until a colloid is formed, drying the colloid, mixing the dried colloid with kaolin, and obtaining a carrier through kneading, extrusion molding, drying and calcination; (2) taking a nickel salt, a manganese salt and a zinc salt as active components, taking a calcium salt as an auxiliary component, dissolving the active components and the auxiliary component in deionized water to obtain a salt solution, adding n-hexane into the salt solution and stirring uniformly to prepare an impregnation solution, immersing the carrier in the impregnation solution, and obtaining the catalyst through washing, drying and calcination. The catalyst prepared by the method is mainly used in a liquid-phase refining reaction process of crude octanol, and has high activity stability and selectivity.

The invention relates to the field of water treatment, and discloses a scale and corrosion inhibitor for seawater circulating cooling water, which is prepared from phosphonic acid grafted maleic anhydride-acrylic acid copolymer, hydroxyethylidene diphosphonic acid, amino trimethylene phosphonic acid, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N- The anti-corrosion coating is prepared from the following raw materials: N, N-diethylaminomethyl-benzotriazole, gamma-aminopropyltriethoxysilane, zinc salt and a polyoxyethylene-polyoxypropylene block copolymer. The core of the invention is that all the raw material components form the thermo-sensitive polyelectrolyte compound through a self-assembly process. The compound is stably dispersed at low temperature by utilizing the cloud point effect of the block copolymer, and is subjected to phase change and preferential deposition on a high-temperature heat exchange surface, so that targeted and efficient delivery of various active components is realized. According to the invention, the problems of incompatibility of components and poor stability of a traditional compound agent are solved, the product has excellent storage stability, and efficient and synergistic corrosion and scaling control can be realized under high-temperature and high-salinity working conditions.

The invention discloses an electrolyte for regulating interface reaction based on an organic anion mediated gradient ion pump, and belongs to the field of zinc metal batteries. The electrolyte for regulating and controlling the interface reaction based on the organic anion mediated gradient ion pump comprises a mixed aqueous solution of zinc salt electrolyte and organic anion salt, the zinc salt electrolyte is selected from any one of zinc sulfate, zinc chloride, zinc acetate or zinc trifluoromethanesulfonate; an organic chain in the organic anion salt is of a Janus structure, the organic chain contains hydroxyl and alkyl with hydrophobic end chain parts, the problems that an interfacial film of an existing aqueous zinc metal battery solid electrolyte is prone to failure, a zinc negative electrode is poor in stability, and side reaction is serious are solved, the high-reversibility and long-life zinc deposition / stripping process is achieved through multiple effects of the organic salt additive, and the service life of the solid electrolyte is prolonged. The overall performance of the zinc metal battery is improved.

The invention belongs to the technical field of daily chemical products, and particularly relates to a hidroschesis, cooling and deodorization composition as well as a preparation method and application thereof. The hidroschesis, cooling and deodorization composition comprises the following components in parts by weight: 10-55 parts of zinc ricinoleate, 1-11 parts of a cooling agent and 10-55 parts of a plant extract, the plant extract is at least one of lemon fruit extract, equisetum arvense extract, mangnolia officinalis bark extract and phellinus linteus extract. The cooling, antiperspirant and deodorant composition provided by the invention takes the zinc ricinoleate, the menthol and the menthol oxypropylene glycol as main cooling and antiperspirant components, and is matched with various plant extracts to exert the auxiliary bacteriostatic, astringing, anti-allergy and anti-allergy effects; the effective synergistic effect is achieved in the aspects of hidroschesis, deodorization, bacteriostasis, astringency, allergy relieving and resisting and the like.

The invention discloses a water-based poly-ceramic coating material as well as a preparation method and application thereof. The formula comprises a composite base material (40-45 parts of modified waterborne polyurethane resin and 15-20 parts of a waterborne acrylic emulsion), a synergistic curing system (10-12 parts of a blocked isocyanate curing agent and 0.8-1.2 parts of a latent organic zinc salt accelerant), an organic-inorganic reinforced phase (10-15 parts of nano silicon dioxide and 8-10 parts of polysilazane) and a functional aid. The base material and the cosolvent cooperate to make VOCs less than or equal to 30 g / L, a curing system cooperates to realize low-temperature rapid curing, organic-inorganic components cooperate to form a poly-ceramic structure, the coating is adaptive to an existing roll aluminum production line, and the problems of environmental protection, energy conservation and performance of a traditional coating are solved.

The invention relates to the technical field of gel electrolyte, in particular to a method for constructing gel electrolyte on the surface of an electrode through in-situ self-initiation and application of the method. The method comprises the following steps: (1) dissolving a zinc salt in water to obtain a liquid electrolyte; (2) uniformly mixing a gel monomer, an initiator, a cross-linking agent and a liquid electrolyte to obtain a precursor solution; and (3) pouring the precursor solution on the surface of the negative electrode of the battery, covering the precursor solution with the positive electrode of the battery, and standing to realize in-situ construction of the gel electrolyte on the surface of the electrode. The solution is gelatinized through reducibility self-initiation of the metal electrode and is constructed on the surface of the electrode in situ, the electrochemical performance of the aqueous zinc metal is remarkably improved, meanwhile, the process steps are reduced, and the cost is reduced.

The invention discloses an electrolyte for improving the cycling stability of a zinc-sulfur battery and application of the electrolyte in a photoelectric storage integrated battery. The electrolyte comprises a solvent, an additive and zinc salt, the additive is iodide, and the iodide comprises iodine negative ions and positive ions or polar functional groups. The functional additive is added into the electrolyte, positive ions inhibit dendritic crystals and side reactions of zinc, and iodine negative ions accelerate reversible change between sulfur and zinc sulfide, so that the cycling stability of the zinc-sulfur battery is improved. A zinc-sulfur battery with high specific capacity and long cycle life is integrated with a solar battery, so that the photoelectric storage integrated battery with high overall conversion efficiency, high specific capacity and long cycle life is prepared.

The invention relates to an electrolyte for synergistically stabilizing positive electrode iodine multi-electron reaction through four-combination zinc salt and a high-surface-capacity zinc-iodine soft package battery. The electrolyte comprises the four-combination zinc salt and water, in the electrolyte, the total concentration of zinc ions in the four combinations of zinc salts is 2 + / -0.2 mol / L; the four-combination zinc salt is a four-combination zinc salt; the SO4 < 2-> in the electrolyte buffers the pH value of a system, so that side reaction of a negative electrode is reduced; cH3COO <-> can be cross-linked with I3 <->, so that shuttling of polyiodide is inhibited, and reversibility of a two-electron reaction is enhanced; bromide ions Br <-> in the electrolyte are chemically combined with I < + > through isohalogen to excite four-electron reaction; the trifluoromethanesulfonate OTf <-> with strong electronegativity surrounds the positive electricity I < + > by virtue of an ion atmosphere effect, so that active water molecule attack hydrolysis failure is avoided, a synergistic stable positive electrode iodine multi-electron reaction is realized, and the high-surface-capacity zinc-iodine soft package battery is beneficial to promoting the development of the zinc-iodine battery to practical application.

The application discloses a carbon nitride / carbon felt electrode for a vanadium redox flow battery and a preparation method thereof, and belongs to the technical field of battery materials. The preparation method comprises the following steps: (1) soaking carbon felt in an ethanol solution containing an iron salt compound and then drying; (2) suspending the dried carbon felt in a closed container, adding a pyrrole monomer, and reacting at a constant temperature under an inert atmosphere to obtain a polypyrrole / carbon felt, which is cleaned and dried; (3) soaking the polypyrrole / carbon felt in an ethanol solution containing a zinc salt compound and then drying; (4) gradually increasing the temperature of the dried polypyrrole / carbon felt under an inert atmosphere to perform high-temperature carbonization, and obtaining carbon nitride / carbon felt; and (5) performing pickling and water washing on the carbon nitride / carbon felt, and obtaining the carbon nitride / carbon felt electrode after drying. In the application, the iron salt is used to catalyze the polymerization and deposition of pyrrole on the surface of the carbon felt, and finally high-temperature carbonization is performed to form various nitrogen-doped structures on the surface of the carbon felt, so that the liquid affinity and the electrochemical reaction activity of the electrode surface are significantly improved, and the energy efficiency of the battery is improved.

The invention discloses an organic long-chain zinc salt for a zinc secondary battery electrolyte and a preparation method and application thereof. The organic long-chain zinc salt comprises a long-chain group, an acidic group and zinc ions, the long-chain group comprises at least one of substituted or unsubstituted C8-16 alkyl groups, and the acidic group comprises at least one of a sulfonic acid group, a phosphoric acid group and a sulfuric acid group. The organic long-chain zinc salt serving as an electrolyte salt of the zinc secondary battery can be adsorbed on the surface of zinc to form a protective layer, so that the cycle life and the capacity retention ratio of the zinc secondary battery are effectively improved.

The invention relates to the technical field of nano-catalysts, and discloses a preparation method and application of a ZnxCd1-xS nano-catalyst rich in sulfur vacancies, the preparation method of the ZnxCd1-xS nano-catalyst rich in sulfur vacancies is characterized by comprising the following steps: S1, mixing cadmium salt, zinc salt and thiourea in deionized water to obtain a mixed solution; and S2, putting the mixed solution into a reaction kettle for heating reaction, cooling, collecting a reaction product, washing the reaction product with deionized water, and drying the washed reaction product to prepare the ZnxCd1-xS nano-catalyst. The ZnxCd1-xS nano-catalyst synthesized by the method is uniform in dispersion, uniform in size and regular in morphology, the morphology of the obtained ZnxCd1-xS nano-catalyst is evolved into a litchi-shaped transition state with a rough surface from a spherical shape along with the rise of the reaction temperature, and then a pine tree-shaped morphology with the regular morphology is generated. In addition, the prepared catalyst is rich in certain sulfur vacancies, and the performance is remarkably improved when the catalyst is applied to the field of photocatalytic hydrogen evolution.

The invention provides an aqueous zinc ion battery electrolyte, a preparation method thereof and a zinc ion battery, and belongs to the technical field of aqueous zinc ion batteries. The aqueous zinc ion battery electrolyte comprises an additive, an inorganic zinc salt and a solvent, the additive comprises at least one of trimethylamine substituted by 1-3 substituent groups, benzene and C3-C10 straight-chain alkane, and the substituent groups comprise phosphonic acid groups or phosphinic acid groups; the solvent comprises a sodium chloride aqueous solution. By adopting the additive with a specific structure and the solvent containing the sodium chloride aqueous solution, the cycle performance of the zinc negative electrode in the water-based zinc ion battery can be remarkably improved, and the service life of the water-based zinc ion battery is prolonged.

This invention provides a method for preparing (002) crystal-plane oriented metallic zinc and its application. The invention employs a two-electrode electrochemical deposition technique, using iron foil, titanium foil, or copper foil as the working electrode, commercial zinc foil as the counter electrode, and an aqueous zinc salt solution as the electrolyte. Constant current density discharge deposition is used to deposit (002) crystal-plane oriented metallic zinc on the working electrode; the constant current density is 50 mA cm⁻¹. ‑2 ~200 mA cm ‑2 The (002) crystal-plane oriented metallic zinc prepared by this invention can be used in rechargeable zinc-ion batteries. The two-electrode electrolytic cell device used in the preparation of metallic zinc in this invention is simple, the preparation process is straightforward, and the preparation method is more universal. The (002) crystal-plane oriented metallic zinc prepared according to the method of this invention can suppress zinc dendrite growth and hydrogen evolution, thereby improving the service life of rechargeable zinc-ion batteries.

The invention relates to the technical field of aqueous zinc ion batteries, in particular to an aqueous zinc ion battery electrolyte as well as a preparation method and application thereof. The invention provides an aqueous zinc ion battery electrolyte. The aqueous zinc ion battery electrolyte comprises soluble zinc salt and fulvic acid, and the concentration of the fulvic acid in the electrolyte is 0.01-50 g / L; wherein rich oxygen-containing functional groups contained in fulvic acid molecules can serve as strong coordination sites to be combined with Zn < 2 + > to generate coordination, so that the migration rate of zinc ions is effectively reduced, and uniform deposition of the zinc ions on the surface of the negative electrode is promoted; meanwhile, direct contact between water molecules and the zinc negative electrode can be reduced by utilizing a molecular interface layer formed by fulvic acid molecules on the surface of the zinc negative electrode, so that water-induced side reaction can be relieved. And the cycle stability of the battery is improved through the effects. In addition, the fulvic acid is wide in source, low in cost and environment-friendly, the production cost of the water-based zinc ion battery is reduced, and large-scale application of the water-based zinc ion battery is promoted.

The embodiment of the invention provides an electrolyte, a preparation method thereof and an aqueous zinc ion battery, the electrolyte comprises a zinc salt and an electrolyte additive, the electrolyte additive comprises a complex formed by an amine ligand and a reducing metal, and the activity of the reducing metal is weaker than that of zinc. When the electrolyte is applied to the aqueous zinc ion battery, the hydration degree and the deposition overpotential of the zinc ion can be reduced, the reversible reaction can be promoted, and a stable protection layer can be generated on the surface of a zinc negative electrode, so that the zinc dendrite growth and the corrosion side reaction are inhibited, the stability of the zinc negative electrode is improved, and the cycling stability of the aqueous zinc ion battery is improved.

The invention relates to the technical field of zinc-iodine battery electrolyte, in particular to aqueous zinc-iodine electrolyte as well as a preparation method and application thereof. The aqueous zinc-iodine battery electrolyte contains an additive and a zinc salt, the molar concentration of the additive is 0.15 M to 0.8 M, and the additive is selected from one or more of triethylamine hydrochloride, 1-butyl-1-methylpyrrolidine chloride, 1, 3-dimethylimidazole chloride, pyridine hydrochloride, aniline hydrochloride, guanidine hydrochloride and 1-ethyl-3-methylimidazole chloride. The method can directionally regulate and control zinc negative electrode deposition and iodine positive electrode reaction kinetics, realizes four-electron reversible conversion, promotes uniform deposition of zinc ions and inhibits side reactions during charging, inhibits multi-iodide shuttle and I < + > hydrolysis during discharging, and has wide application prospects in the zinc-iodine battery electrolyte industry.

The present application relates to a kind of composite phosphorus-free scale inhibitor and its preparation method, including 800-1200 parts by weight of desalted water, 1-3 parts by weight of modified lignin sulfonate, 2-4 parts by weight of calcium magnesium acetate, 0.5-1.5 parts by weight of azole, 400-600 parts by weight of soluble inorganic zinc salt and 50-150 parts by weight of copolymer A.The composite phosphorus-free scale inhibitor provided by the present application is clear and transparent concentrate, after the above concentrate is added to circulating water, the effective ingredient in it can form soluble chelate with Ca 2+ , Mg 2+ Forming, increase the saturation solubility of ion, hinder micro-fouling lattice formation, distort crystal growth, so that microcrystalline will not accumulate into scale, and can make old scale loose, gradually shed old scale;At the same time, the special corrosion inhibitor and other corrosion inhibitor produce synergistic effect, which can effectively control the pitting of stainless steel, achieve the purpose of preventing scale, and fundamentally reduce the efficiency of corrosion and scale inhibition.

The invention relates to a porous nickel-iron alloy integrated electrode and a preparation method and application thereof, and belongs to the technical field of electrochemistry. The preparation method comprises the following steps: carrying out cleaning pretreatment on a stainless steel mesh substrate; then electro-deposition is carried out in a solution containing ferric salt and nickel salt, and a nickel-iron alloy layer is formed; carrying out secondary electro-deposition in a solution containing zinc salt, and carrying out high-temperature calcination treatment to obtain a nickel-iron-zinc alloy; and finally, the zinc component is removed through selective corrosion of an alkaline solution, and the nickel-iron alloy integrated electrode with the porous structure is formed on the stainless steel mesh. The method is controllable in process, and a porous structure which is high in specific surface area and beneficial to mass transfer is effectively constructed through step-by-step electro-deposition, calcination and corrosion treatment. The obtained integrated electrode can be directly used as an alkaline water electrolysis oxygen evolution reaction (OER) anode, shows high electrocatalytic activity and stability, and is suitable for the fields of water electrolysis hydrogen production and the like.

The invention discloses an aqueous zinc-vanadium battery electrolyte preparation method and a battery, and belongs to the technical field of aqueous zinc ion batteries. The preparation method comprises the following steps: preparing a polyquaternium aqueous solution; and adding soluble zinc salt into the polyquaternium aqueous solution, stirring and dissolving to obtain the composite electrolyte. According to the electrolyte, through the synergistic effect of the polyquaternary ammonium salt and the zinc salt, the acidity and water activity of a system are effectively reduced, dendritic crystal growth and hydrogen evolution reaction of a zinc negative electrode are inhibited, meanwhile, a nitrogen-containing protective layer is formed on the surface of a vanadium positive electrode, and vanadium dissolution is reduced. The battery containing the electrolyte shows excellent cycle stability in a wide temperature range of-20 to 80 DEG C, the cycle life of the zinc symmetric battery exceeds 3000 hours, the capacity retention rate of the whole battery after 4000 cycles reaches 87.6%, and the technical problems of aggravation of interface side reaction and fast degradation of battery performance under high-temperature and high-acidity conditions are solved.

The invention discloses a preparation method and application of a high-entropy layered double hydroxide oxygen evolution catalyst, and relates to the field of oxygen evolution reaction catalysis, and the preparation method comprises the following steps: S1, washing foamed nickel in absolute ethyl alcohol and deionized water, and then carrying out ultrasonic treatment in a hydrochloric acid solution to obtain pretreated foamed nickel; s2, adding ferric salt, cobalt salt, nickel salt, manganese salt, zinc salt and a proper amount of urea into deionized water, then adding ammonium fluoride, and uniformly stirring to obtain a mixed solution; and S3, transferring the mixed solution and the pretreated foamed nickel into a reaction kettle, carrying out a hydrothermal reaction, and washing and drying the obtained product to obtain the high-entropy layered double hydroxide oxygen evolution catalyst. According to the method, the key regulation and control effect of NH4F on the structure, chemical and electro-catalytic properties of HELDHs in the synthesis process of the HELDHs is analyzed, and the performance enhancement is attributed to NH4F-induced morphology and crystal engineering and catalytic active cation vacancies generated in situ through selective leaching of Zn < 2 + > and adsorption of sulfate under the alkaline condition.

This invention discloses a composite nanozyme that enhances the clinical efficacy of oxaliplatin, its preparation method, and its application. The composite nanozyme consists of indium ruthenium nanozyme and an iliximab embedding and anchoring layer. The indium ruthenium nanozyme consists of indium ruthenium nanoparticles and a carbon-nitrogen framework, with the indium ruthenium nanoparticles loaded on the surface and within the pores of the carbon-nitrogen framework. The iliximab embedding and anchoring layer consists of a dithiol polyethylene glycol coating layer and iliximab. Preparation method: ZIF-8 is prepared by co-precipitation of zinc salt methanol solution and 2-methylimidazole methanol solution, followed by calcination to obtain the carbon-nitrogen framework. The carbon-nitrogen framework dispersion is then stirred in an oil bath with indium nitrate solution and ruthenium trichloride solution to prepare a nanozyme precursor, followed by calcination to obtain indium ruthenium nanozyme. The indium ruthenium nanozyme is dispersed in a dithiol polyethylene glycol solution, and iliximab solution is added dropwise. The resulting solid product is then dried. This invention can solve problems such as strong drug tolerance, insufficient intracellular accumulation, and severe tumor immunosuppression in oxaliplatin treatment.

The application belongs to the field of rechargeable secondary batteries, and particularly relates to a water-based zinc ion battery capable of working in a wide temperature range, which is composed of a positive electrode, a negative electrode and an electrolyte. The positive electrode material is an n-type organic substance; the negative electrode is a metal zinc foil or a metal zinc powder; the electrolyte takes deionized water as a main solvent, takes inorganic lithium salt or inorganic sodium salt and a small amount of organic zinc salt as solutes, has the characteristics of high boiling point and low freezing point, and shows good ion conductivity in a relatively wide temperature range (-40 DEG C to 100 DEG C). Different from traditional zinc ion batteries, the zinc ion battery proposed in the application can stably work in the temperature range of -40 DEG C to 100 DEG C, shows good rate performance and cycle stability, and can be used for large-scale energy storage devices in extreme environments such as military and aerospace.

The present application relates to the technical field of carbon material preparation, and particularly relates to a preparation method of nitrogen-doped ultrathin nanosheet support microspherical carbon material. The preparation method of the microspherical carbon material comprises the following steps: mixing gallium salt, zinc salt, carbon precursor, amine compound and water, and performing a solvothermal reaction to obtain deep red powder solid; and then performing calcination on the deep red powder solid in an inert atmosphere, and performing acid washing, water washing and drying to obtain the microspherical carbon material. The residual template agent after calcination can be removed completely by using dilute hydrochloric acid, thereby avoiding the use of strong corrosive reagents such as HF, KOH or NaOH. The method realizes batch production of the synthesis of the nitrogen-doped ultrathin nanosheet support microspherical carbon material, is simple to operate, stable in process, and regular in product morphology, and the amount of gallium salt and amine compound is reduced. The Pd(OH)2 / C catalyst prepared by using the material as a carrier shows excellent catalytic activity in the hydrogenolysis debenzyl reaction of a cage-shaped substrate.

The present application relates to the technical field of copper clad laminates, and discloses a copper clad laminate, a resin composition for the copper clad laminate, and spherical silicon and a preparation method therefor. The spherical silicon of the present application is composed of spherical silicon dioxide and zinc molybdate particles dispersedly grown on the surface of the spherical silicon dioxide in situ and has a diameter of less than 10 microns and a D50 of 0.6-6 microns. The content of zinc molybdate per unit area on the surface of the spherical silicon dioxide is 0.03-1 g / m2, and the size of the zinc molybdate particles is less than or equal to 400 nm. The preparation method comprises: enabling spherical silicon dioxide to come into contact with / be mixed with a soluble molybdate and a zinc salt in an aqueous reaction system; and reacting the soluble molybdate with the zinc salt in situ on the surface of the spherical silicon dioxide, so as to form spherical silicon chemically coated with zinc molybdate particles. In the present application, by directly synthesizing the zinc molybdate in situ on the surface of the spherical silicon dioxide by means of a hydrothermal method, the structural morphology of the obtained spherical silicon and the size of the zinc molybdate particles can be effectively controlled, thereby ensuring that the wear of a drill bit during the drilling of the copper clad laminate is effectively mitigated.

Provided is dental glass having sufficient antibacterial properties through the inclusion of zinc. This dental glass contains 41-52 mass% of ZnO, 47-51 mass% of P2O5, 7 mass% or less of MgO, and 9 mass% or less of CaO. The fluorine content in the dental glass is preferably 3 mass% or less. The dental glass can be easily produced through a mixing step for mixing a starting material solution containing a zinc salt solution, a phosphate solution, an optional magnesium salt solution, and an optional calcium salt solution to form aggregates in the starting material solution, and a drying step for drying the aggregates to obtain a powder.

The invention relates to the technical field of catalyst preparation, and discloses a carbon modified copper-based catalyst and a preparation method and application thereof. The method comprises the following steps: (1) sequentially carrying out coprecipitation and aging on an alkaline precipitant solution, a metal salt solution and an anion modifier solution to obtain an intermediate product I; and (2) under the condition that the oxygen concentration is not higher than 5% by volume, roasting the intermediate product I to obtain the carbon modified copper-based catalyst, the anion modifier solution contains sodium dodecyl diphenyl ether disulfonate and sodium gluconate in a molar ratio of 1: (1-10); the pH value of the anion modifier solution is 9-11; the metal salt solution contains zinc salt, copper salt and aluminum salt. The prepared carbon modified copper-based catalyst has the advantages of high conversion per pass of carbon dioxide, low activation temperature, high methanol selectivity, long-period operation and stable structure.

The invention belongs to the technical field of wastewater treatment, and discloses an efficient evaporative crystallization treatment process for zinc-containing wastewater, which comprises the following steps: 1) adding a hydrogen peroxide solution into the zinc-containing wastewater, and applying ultrasonic waves to carry out ultrasonic enhanced oxidation; 2) stopping ultrasonic treatment, introducing sulfate radicals into the zinc-containing wastewater, adjusting the pH value, precipitating, separating the precipitate, adding a chelating agent and an anti-scaling agent into the zinc-containing wastewater, stirring for reaction, separating the precipitate, and then performing microfiltration to obtain pretreated zinc-containing wastewater; 3) feeding the pretreated zinc-containing wastewater into a multi-stage flash evaporation system to obtain a zinc-containing concentrated solution; 4, the zinc-containing concentrated solution is fed into a crystallizer, microbubbles are introduced, meanwhile, ultrasonic waves are applied to enhance gas-liquid interface disturbance to promote crystallization, crystals are separated from crystallization liquid and then dried, and the zinc salt is obtained.The technology achieves the multiple purposes of low scaling rate, low energy consumption, high recovery rate and high zinc salt purity, and has excellent industrial implementability and popularization value.