65results about How to "Promote decomposition reaction" patented technology

The invention discloses a resin bendable grinding wheel and a preparation method and a device thereof. The resin bendable grinding wheel consists of brown aluminium oxide, calcined alumina, white alundum, black silicon carbide, phenolic resin powder, phenolic resin liquid, cryolite, barium sulphate, pyretic, iron oxide red, Hunori gel, alkali-free high tensile glass fiber mesh and non-woven black cloth. Compared with the prior art, through the optimization configuration on the aspect of the material selection and working procedures, the strength, the flexibility and the aging resistance of the grinding wheel are greatly improved, and at the same time, the resource and the energy are saved; and the strength of the grinding wheel is more than 80m/s, the grinding ratio is more than or equal to 1:15, the maximum bendable angle can reach 40 degrees, the tensile strength is greatly improved, the service life is prolonged by two times, the energy consumption is reduced by 5 to 10 percent, and the yield of the finished product can reach more than 99 percent.

The invention provides a preparation method of a transition metal phosphide/core-shell nitrogen-doped carbon nanofiber composite material. The preparation method includes preparing a carbon nanofiberaccording to an electrospinning technique by taking a carbon-containing high-molecular polymer as a carbon source, coating the carbon nanofiber with an electroconductive polymer through surface polymerization, loading an MOF material onto the surface of the carbon nanofiber coated with the electroconductive polymer according to an in-situ growth method to obtain a precursor, and subjecting the precursor to high-temperature carbonizing and phosphating to obtain the transition metal phosphide/core-shell nitrogen-doped carbon nanofiber composite material. Activity test results show that the transition metal phosphide/core-shell nitrogen-doped carbon nanofiber composite material prepared by the preparation method has high electrocatalytic activity for total decomposition reaction of HER, OER and water and has high stability in acid-base media, thereby being a dual-functional catalyst that can replace precious metal and having a good development prospect in water electrolysis reaction.

The invention provides a landfill leachate processing process. Landfill leachate sequentially passes through a pretreatment system, a main body biological treatment system and a deep treatment system; the pretreatment system consists of a regulating pool, an adsorption pool and a coagulating pool; wastewater is pretreated sequentially through the devices; outlet water enters the main body biological treatment system; the main body biological treatment system comprises an anaerobic EGSB (expanded granular sludge bed) reactor, an A/O short-range nitratlon reaction pool and an anaerobic ammonia oxidation UASB (upflow anaerobic sludge blanket) reactor; the treatment devices perform real-time regulation control through a PLC (programmable logic controller) control system for denitrification decarbonization reaction; the outlet water enters the deep treatment system for further treatment; the deep treatment system comprises a secondary coagulating pool, a primary homogeneous catalysis ozone oxidation reaction pool, a MBR (meane biological reactor) secondary biological reaction pool and a secondary homogeneous catalysis ozone oxidation reaction pool; finally, organic matters, total nitrogen and ammonia nitrogen of the outlet water reach the discharge standard. The landfill leachate processing process has the advantages that efficient denitrification and carbon removal are realized; the energy is saved; the consumption is reduced; the operation is stable; meanwhile, the goal of zero concentrated liquid generation is realized.

Disclosed is an electrolyte solution which enables to improve battery characteristics such as battery swelling and charge/discharge efficiency. Also disclosed is a battery using such an electrolyte solution. Specifically disclosed is a battery wherein a positive electrode (21) and a negative electrode (22) are arranged in layers via an electrolyte layer (24). The electrolyte layer (24) is a gel containing an electrolyte solution and a polymer compound, and the electrolyte solution contains a compound having a proton-collecting function such as hexamethylenetetramine or hexaethylenetetramine. Consequently, a free acid such as hydrofluoric acid can be captured, thereby suppressing decomposition reaction of the electrolyte.

The invention relates to a method for preparing aromatic hydrocarbon from methanol or dimethyl ether and mainly aims to solve the problems of low yield of aromatic hydrocarbon, serious heat release during reaction, rapid increase of temperature of a reactor and rapid deactivation of a catalyst in the aromatization process of methanol or dimethyl ether. According to the technical scheme of the invention, methanol or dimethyl ether as a raw material is enabled to be in contact with a reaction accelerator, a heat balance agent and a catalyst in a fixed bed reactor at the reaction temperature of 350-650 DEG C, and products of reaction are separated to obtain the methanol or dimethyl ether containing aromatic hydrocarbon. By adopting the technical scheme, the problems can be well solved. The method provided by the invention can be applied to the industrial production of aromatic hydrocarbon through conversion of oxygenated chemicals.

The invention relates to a method for preparing high-strength sulphoaluminate cement and co-producing sulfuric acid. The method comprises the following steps of adopting phosphogypsum for completely replacing limestone and natural gypsum, milling and homogenizing the phosphogypsum, bauxite, steel scoria, silica and pulverized anthracite, and then calcinating the milled and homogenized raw materials at a temperature of 1250-1300 DEG C. The method is capable of greatly improving the phosphogypsum utilization ratio, and high-concentration sulfur dioxide tail gas can be adsorbed to prepare sulfuric acid. The prepared sulphoaluminate cement clinker is high in hardening rate, high in early-stage strength, and stable in later-stage strength increase; performance tests indicate that the mechanical strength of the sulphoaluminate cement prepared by the method conforms to the rapid-hardening sulphoaluminate cement standard.

The invention discloses a cuprous oxide-based photocathode with an enhanced nitrogen-doped back surface electric field, wherein the structure of the photocathode comprises conductive glass, a nitrogen-doped cuprous oxide layer, a P-type cuprous oxide light absorption layer, an N-type layer, a titanium dioxide protection layer and a cocatalyst layer from bottom to top. According to the invention, the performance of the cuprous oxide-based photocathode is greatly enhanced, so that the photocurrent of the planar cuprous oxide-based photocathode under a bias voltage of 0 V vs.RHE reaches about 10mA cm<-2> and is close to a theoretical value of 14 mA cm<-2>; and the introduction of the nitrogen-doped cuprous oxide layer can replace a traditional precious metal back electrode (gold electrode) so as to substantially reduce the preparation cost of the device, so that the cuprous oxide-based photocathode has a good development prospect, and the commercial application of the cuprous oxide-basedphotocathode is expected to be promoted.

The invention relates to a combined production method for preparing sulphoaluminate cement and sulfuric acid from flue gas desulfurization gypsum. According to the method, flue gas desulfurization gypsum which replaces limestone and natural gypsum completely is mixed with bauxite, silica and anthracite, and the sulphoaluminate cement is obtained after calcinations. The method can improve the utilization rate of flue gas desulfurization gypsum by a large margin, and the tail gas containing sulfur dioxide with a higher concentration can be absorbed to prepare sulfuric acid; the prepared sulphoaluminate cement clinker is fast in rate of hardening, high in early strength and further promotes the stability of later strength; through the performance tests, it is indicated that the mechanical strength of the sulphoaluminate cement prepared by the method meets the standard of rapid hardening sulphoaluminate cement.

The invention relates to a method for preparing hydrogen, and in particular relates to a method for preparing hydrogen by the electrocatalysis of a sodium borohydride solution. The method comprises the following steps: leading the sodium borohydride solution with the mass concentration of 0.1% to 35% into an electrolytic tank with a cathode electrode and an anode electrode; performing the electrocatalysis by applying a direct current voltage; and then performing a catalytic decomposition on the sodium borohydride solution on the surfaces of the electrodes, thereby generating the hydrogen. By utilizing the sodium borohydride solution and the direct current voltage, the transferring of electric charges on the interfaces of the electrodes and electrolytes is accelerated, so that the catalytic activity of electrode materials is improved; and by utilizing the electrocatalysis of the electrodes, the decomposition reaction of the sodium borohydride solution is promoted, so that the hydrogen is prepared in the electrocatalysis manner. The electric energy required by the electrocatalysis is far less than that required by the water decomposition, so that the electric energy is saved. Compared with the method for preparing the hydrogen by the catalytic decomposition of the sodium borohydride by directly utilizing commonly-used catalysts such as acid materials or metal catalysts, in the method provided by the invention, the starting and the ending of hydrogen generation as well as the hydrogen generation yield can be regulated through the current and the voltage between the electrodes, so that the controllability is improved greatly. In addition, the method provided by the invention is safe, environment-friendly and free of oxygen generation.

The invention discloses a high-voltage lithium cobalt oxide lithium ion battery non-aqueous electrolyte, which comprises a non-aqueous organic solvent, an electrolyte lithium salt and an additive, and the additive comprises at least one imidazole salt compound with a specific structure or an isocyanurate compound with a specific structure. The invention also discloses a lithium ion battery comprising a positive plate, an isolating membrane, a negative plate and the non-aqueous electrolyte of the high-voltage lithium cobalt oxide lithium ion battery. The imidazolium salt additive in the electrolyte can participate in negative electrode film forming, the dynamic performance and thermodynamic performance of a negative electrode are improved, and a formed passive film is low in impedance; the isocyanurate additive can be preferentially oxidized and decomposed on a positive electrode material interface under a high voltage condition to form a passive film, so that the oxidative decomposition of the carbonic ester solvent under the high voltage is avoided; and the fluorine cyanogen ester substance is used as the solvent, so that the electrochemical window of the electrolyte can be widened better.

The invention discloses a preparation method of modified anti-felting wool fiber. The method particularly comprises the following steps that 1, an oxidative antibacterial solution is prepared; 2, theoxidative antibacterial solution is added into a stirring tank, water bath heating is conducted to reach 40-45 DEG C, and the wool fiber is poured into the stirring tank; 3, compound enzymatic hydrolysate is prepared; 4, the wool fiber processed in step 2 is soaked in the compound enzymatic hydrolysate, and a normal temperature enzymatic hydrolysis reaction is conducted; 5, a chitosan solution isprepared and added into the stirring tank, the wool fiber prepared in step 4 is added, stirring is conducted for 5 h and then fished out, and then air-drying is conducted at normal temperature. Accordingly, the wool fiber is oxidized, protein of the wool fiber is exposed, the exposed protein is subjected to enzymolysis through protease, by means of enzymolysis, negative ions on the surface of thewool fiber are increased, chitosan is adsorbed to the surface of the wool fiber conveniently, and the texture is soft while the wool fiber anti-felting property is improved.

The invention provides a preparation method of single crystal gallium oxide and process equipment for preparing the single crystal gallium oxide. The preparation method of the single crystal gallium oxide comprises the following steps: providing gallium oxide powder; pressing the gallium oxide powder into blocky gallium oxide; a crucible is provided, a bottom containing area and a top opening area are arranged in the crucible, and the bottom containing area and the top opening area are spaced; placing the block gallium oxide into the bottom accommodating area, and placing a seed crystal in the top opening area; the crucible is placed in a flowing protective atmosphere, the crucible is heated, the temperature applied to the top opening area is lower than the decomposition temperature of the seed crystal, and the temperature applied to the bottom containing area is higher than the decomposition temperature of the block gallium oxide. According to the method, the speed of decomposing the gallium oxide into the gas source is increased, so that the continuous growth speed of the single crystal gallium oxide is increased, the energy is saved, and the production cost is reduced.

The invention relates to the technical field of environmental protection, in particular to integrated equipment for the efficient treatment of the volatile organic waste gas. The equipment comprises ashell arranged on a base, wherein an electronic control cabinet is arranged in the shell, the interior of the shell is successively provided with a filtering module, a UV lamp module, an activated carbon module, an ozone removal module and an air-pumping module which are connected in a closed manner, the filtering module and the air-pumping module are arranged at the upper part of the interior ofthe shell, the UV lamp module, the activated carbon module and the ozone removal module, which can be disassembled, are arranged at the lower part of the interior of the shell, the upper part of thefiltering module is provided with a waste gas inlet, and the upper part of the air-pumping module is provided with a gas discharge outlet. The external waste gas is subjected to the dust removal by the filtering module, the waste gas decomposition and deodorization by the UV lamp module, the adsorption of the incompletely oxidized organic waste gas by the activated carbon module, the decompositionof the excess ozone by the ozone removal module, and discharge up to standard by the air-pumping module. The equipment integrates dust removal, VOCs waste gas treatment and ozone removal together, and has no secondary pollution and high purification efficiency.

The invention relates to a method for preparing sulphate aluminium cement through phosphogypsum. The method includes the steps that limestone and natural gypsum are completely replaced with the phosphogypsum, the phosphogypsum is subjected to powder grinding and homogenized through bauxite, solid waste steel residues and anthracite and calcined at the temperature of 1,250 DEG C to 1,300 DEG C to prepare the sulphate aluminium cement. By means of the method, the using rate of the phosphogypsum can be greatly increased, and high-concentration sulfur-dioxide tail gas can be prepared into sulfuric acid through absorption. The hardening speed of sulphate aluminium cement clinker prepared with the method is high, the earlier-stage strength is high, the later strength is also enhanced to be stable, and performance testing indicates that the mechanical strength of the sulphate aluminium cement prepared with the method meets the standard of the sulphate aluminium cement.

The invention discloses a super-long slump-retaining polycarboxylic acid pumping agent, which is prepared from the following components in parts by weight: 15 to 20 parts of water-reducing polycarboxylic acid superplasticizer, 10 to 15 parts of slump-retaining polycarboxylic acid superplasticizer, 1 to 3 parts of reaction type hydration regulator, 0.01 to 0.2 part of air entraining agent, 0 to 2 parts of retarder, 0.5 to 2.5 parts of auxiliary retention agent, 0.3 to 0.8 part of water-retaining agent and the balance of water. Compared with the prior art, a water-reducing polycarboxylic acid superplasticizer and a gradient slow-release slump-retaining polycarboxylic acid superplasticizer which have water-reducing and retaining properties are adopted as mother liquor, so that gradient slow release in a cement system is possible, super-long slump retaining of concrete can be realized, and possibility is provided for long pumping in a relatively far construction site or a relatively long pumping pipeline.

The invention discloses a method for preparing sulfur dioxide and calcium oxide through anaerobic thermal decomposition of calcium sulfite. High-purity calcium oxide and sulfur dioxide are obtained through indirect thermal decomposition of intermediate product calcium sulfite in wet desulfurization of flue gas under the anaerobic condition. Thermal decomposition of calcium sulfite comprises an aerobic drying preheating step, a vacuum deoxidation step and an anaerobic thermal decomposition step, wherein aerobic drying preheating can prevent calcium sulfite from being oxidized into calcium sulfate easily in the air at 450 DEG C or above, in the anaerobic thermal decomposition step, deoxidation of dried calcium sulfite in a micro negative pressure state is realized by use of an air lock valveat the lower part of a cyclone separator and a vacuum fan of a thermal-insulating flow stabilization bin. High-temperature anaerobic thermal decomposition of calcium sulfite is realized by use of a three-stage closed screw decomposition furnace, hot air obtained through anaerobic thermal decomposition performs stepped preheating on a three-stage heat preheater, and recycling of energy is realized. The method has excellent economic, environmental protection and social benefits and is suitable for promotion and application.

The invention provides a process method for preparing chlorosulfonyl isocyanate through continuous reactive distillation, and relates to the technical field of fine chemical engineering, and the process method comprises the following steps: enabling sulfur trioxide and cyanogen chloride to enter a reactor for primary reaction; continuously feeding the reaction liquid into a first reactive distillation tower, extracting heavy components from the bottom of the tower, extracting sulfur trioxide and cyanogen chloride which do not react completely from the top of the tower, and extracting a chlorosulfonyl isocyanate crude product liquid containing a small amount of chlorinated pyrosulfonyl isocyanate after preliminary concentration from a side liquid phase; continuously feeding the crude product liquid into a second reactive distillation tower, extracting a small amount of sulfur trioxide and cyanogen chloride generated by decomposing chlorinated pyrosulfonyl isocyanate from the top of thetower, extracting a small amount of heavy components from the bottom of the tower, and extracting a qualified chlorosulfonyl isocyanate product from a side gas phase. The preparation efficiency of thechlorosulfonyl isocyanate is improved.