394 results about "Continuous reactor" patented technology

The present invention relates to a method for preparing an acrylic ester polymer syrup by bulk polymerization, and more particularly, to a method for preparing an acrylic ester polymer syrup, which comprises the steps of: supplying a monomer solution and an initiator solution to a monomer solution reservoir and an initiator solution reservoir, respectively; supplying the monomer solution and the initiator solution to a complete-mixing type continuous reactor, while maintaining the dissolved oxygen in the monomer solution reservoir and the initiator solution reservoir at 0.0001 to 3 ppm, separately or after mixing prior to the supply; and performing bulk polymerization continuously while maintaining the solution mixture supplied to the continuous reactor at 70 to 150 ° C. and 1 to 10 atm, with a mean residence time of 30 to 240 minutes. In accordance with the present invention, an acrylic ester polymer syrup can be obtained with a degree of polymerization of 20 to 70% at a low polymerization temperature, even with a small amount of initiator. Productivity can be improved by reducing reaction time with the use of an initiator having a short half-life and polymerization can be performed very stably and continuously without gelation.

The invention includes methods for producing dianhydrosugar alcohol by providing an acid catalyst within a reactor and passing a starting material through the reactor at a first temperature. At least a portion of the staring material is converted to a monoanhydrosugar isomer during the passing through the column. The monoanhydrosugar is subjected to a second temperature which is greater than the first to produce a dianhydrosugar. The invention includes a method of producing isosorbide. An initial feed stream containing sorbitol is fed into a continuous reactor containing an acid catalyst at a temperature of less than 120° C. The residence time for the reactor is less than or equal to about 30 minutes. Sorbitol converted to 1,4-sorbitan in the continuous reactor is subsequently provided to a second reactor and is dehydrated at a temperature of at least 120° C. to produce isosorbide.

Hydrocarbon feeds can be hydrotreated in a continuous gas-phase environment and then dewaxed in a liquid-continuous reactor. The liquid-continuous reactor can advantageously be operated in a manner that avoids the need for a hydrogen recycle loop. A contaminant gas can be added to the hydrogen input for the liquid-continuous reactor to modify the hydrogen consumption in the reactor.

The invention relates to a production method for preparing 2,5-dichloronitrobenzene (DCNB) through continuous nitration, which particularly realizes the recycling of waste acids in the preparing process. The invention provides a technological program capable of recycling acids for preparing 2,5-dichloronitrobenzene (DCNB) through the continuous nitration, which is characterized in that sulfuric acid and nitric acid are prepared into a mixed acid, the mixed acid and paradichlorobenzene are simultaneously fed into a three-stages kettle (ring) type continuous reactor to carry out nitration reaction, a nitration reaction solution discharged form the third-stage kettle (ring) type continuous reactor is stood for layering so as to obtain a nitrifying oil layer and a nitrifying waste acid, and the nitrifying oil layer is subjected to alkali cleaning, water washing and light component removal so as to obtain a 2,5-DCNB finished product; paradichlorobenzene is added into the nitrifying waste acid to extract organic matters in the acid layer, residual HNO3 in the acid layer is consumed, after the extraction is completed, the obtained product is layered so as to obtain an extraction oil layer and an extracted residual waste acid, the extraction oil layer is used for next-batch nitrification, the extracted residual waste acid after being concentrated and nitric acid are prepared into the waste acid for next-batch nitrification, a small amount of emulsion layer is produced in the process of recycling, and the emulsion layer after being combined with the nitrifying oil layer is subjected to alkali cleaning and water washing.

The invention provides a method for treating sewage by Fenton process, which comprises: adopting a multistage serial reactor or a single-stage continuous reactor; adding a catalyst in the initial stage of a reaction; adjusting the pH value to 1.5 to 6.5; sequentially adding an oxidizer in the multistage serial reactor or adding the oxidizer at a plurality of points along water flow direction in the single-stage continuous reactor; and controlling the total additive amount of the oxidizer calculated by mg/L to be smaller than sewage COD value calculated by mg/L. Compared with the conventional method using a single-stage Fenton process, the method requires a greatly reduced amount of the oxidizer and the catalyst for achieving the same treatment effect and reduces treatment cost.

The invention provides a method for realizing simple and direct preparing of high-efficiency cement rubber additive. The method, which has lower cost and takes ammonia, propylene oxide (PO) and ethylene oxide (EO) as raw materials, comprises the following steps that: superfluous ammonia stream and PO stream are fed into a continuous reactor so as to continuously form a mixture containing isopropanolamine, diisopropanolamine and triisopropanolamine; liquid level inside the continuous reactor is maintained to ensure that the stream in the reactor undergoes outer circulation spraying through a circulating pump from the bottom to the top of the continuous reactor, and part of the stream is continuously fed into a flash tower so as to remove unreacted ammonia; then, the stream with ammonia removed is reacted with EO stream so as to continuously generate products. The method ensures that products do not need rectification separation and greatly reduce production energy consumption, thereby reducing the production cost of products.

A method and apparatus for reacting a plurality of different mixtures in parallel in a semi-batch or continuous mode is provided. Each reaction is contained within a reactor vessel, the reactor vessels combined into a reactor block. Reactant(s) to be added during the reaction are kept in a header barrel, which has a plunger to feed reactant(s) from the header barrel through a transfer line into the reactor vessel. The plunger is moved using a drive system. The header barrels are optionally combined in a header block. The header block is sealed to a plate containing the transfer lines, which in turn is sealed to the reactor block. A latch mechanism is provided for easy sealing of the reactor and header blocks to the plate. The entire apparatus may be placed on a rocker or rotating plate for mixture as the reaction is proceeding.

Method to prepare fluids (liquids and gases) containing pure chlorine dioxide which is not contaminated by the starting materials or the byproducts of the chlorine dioxide synthesis or to deliver pure chlorine dioxide into any medium capable of dissolving chlorine dioxide, wherein the chlorine dioxide generated in the process is transported across a pore free polymeric membrane via selective permeation into the target medium. Apparatus to realize the said method, wherein the generation of chlorine dioxide is carried out in such a reactor where some or all walls comprising the reactor, or the walls of a permeator unit attached to the reactor, are made of the said pore free polymer, characteristically some kind of silicone rubber, which is highly permeable to chlorine dioxide, but which is practically impermeable for the acidic and corrosive reagents used for the chlorine dioxide synthesis, its permeability being at least 3 orders of magnitude lower for these contaminating components compared to that of chlorine dioxide. The invention can be realized both by batch and by continuous reactors.

The invention belongs to the field of chemical production, and provides a method for continuously producing acesulfame potassium, which comprises the following steps: continuously mixing and dissolving sulfamic acid and dichloromethane, continuously neutralizing with a triethylamine solution, introducing the neutralized reaction solution and ketene dimer into a continuous reactor, and carrying outaddition acylation reaction to obtain a DKA reaction solution; sulfur trioxide and solvent micro-mixing: S03, enabling dichloromethane to enter a micro-mixer, so as to prepare a cyclizing agent; cyclization and hydrolysis: continuously feeding the DKA reaction solution and a cyclizing agent into a cyclization microreactor to generate a cyclization reaction solution, and continuously feeding the cyclization reaction solution into a hydrolysis microreactor to obtain an acesulfamic acid reaction solution; enabling the acesulfame acid reaction liquid and dichloromethane to enter continuous extraction equipment, enabling an extracted organic phase and a potassium hydroxide aqueous solution to enter a continuous neutralization reactor to obtain acesulfame acid potassium reaction liquid, and subjecting the acesulfame acid potassium reaction liquid to continuous concentration, continuous crystallization, continuous separation and continuous drying to obtain the acesulfame acid potassium finished product. The process has the characteristics of simple process, low cost, good product quality, continuous whole process and the like.

The invention relates to a novel process for the anionic polymerization of lactams, in which:(a) (i) a catalyst capable of creating a lactamate and (ii) a regulator chosen from the amides of formula R1-NH-CO-R2, in which R1 can be substituted with a radical R3-CO-NH- or R3-0- and in which R1, R2 and R3 denote an aryl, alkyl or cycloalkyl radical, are dissolved in the molten lactam; the temperature of this reaction mixture being between the melting point of the lactam and 15° C. higher in order to ensure its good stability,(b) the solution from step (a) is introduced into a mixing device and is then heated to a temperature which is sufficient to obtain bulk polymerization of the lactam in no more than 15 minutes.(b) is usually a continuous reactor, for example an extruder; however, it can be replaced with a mold.

A system and method for continuous decomposition of organic material to produce biogas and compost in which successive reactor zones in a primary reactor are used in turn to receive organic material which is decomposed in situ anaerobically followed by aerobic decomposition and excavation of raw compost from the same reactor zone where it is received into the organic treatment facility. Organic rich liquor recovered during anaerobic decomposition is further decomposed in a secondary reactor from which spent liquor is returned to the primary reactor while biogas harnessed from both the primary and secondary reactors is treated, and optionally used to fuel the operation of the organic treatment facility or for sale as fuel or electricity.

This invention relates to an improved continuous process for the production of low molecular weight polyoxyalkylene polyether polyols. These polyoxyalkylene polyether polyols have a hydroxyl content of from about 3.4 to about 12.1% by weight, and may also be characterized as having an OH number of from about 112 to about 400. The process comprises establishing oxyalkylation conditions in a continuous reactor in the presence of a DMC catalyst; continuously introducing alkylene oxide and a low molecular weight starter into the continuous reactor; recovering a partially oxyalkylated polyether polyol from the reactor; and allowing the recovered partially oxyalkylated polyether polyol to further reactor until the unreacted alkylene oxide content of the mixture is reduced to 0.001% or less by weight.

An acrylic pressure-sensitive adhesive which is produced by advantageous continuous polymerization and has a reduced low molecular component content and therefore hardly contaminates an adherend, and a process of producing such an adhesive. The process comprises continuously feeding a monomer mainly comprising at least one alkyl (meth)acrylate, a radical polymerization initiator and carbon dioxide to a continuous reactor through a mixer and performing continuous bulk polymerization at a polymerization temperature of 50 to 180° C. for a residence time of 0.5 to 60 minutes in a continuous reaction zone of said reactor.

Disclosed are efficient municipal wastewater treatment apparatus and process characterized in that the nitrogen is removed by nitrification and denitrification reaction in the cyclic aeration reactor wherein Anaerobic state, Anoxic state and Oxic state are change into time concept in a single reactor, and the untreated organic materials are further removed by the 24-hour-continuous reactor.

Production of methacrylic acid consists of amidation, hydrolytic reaction and distillation purification. It is characterized by using a set of continuous reactor comprising reaction vessel, tubing reactor, thermal insulating device and amide acceptor. Its advantages include easy reacting temperature control, short reacting period and higher productivity.

A process for preparing modified polymer by withdrawing a slip stream of polymer melt from the discharge line of a continuous polymerization reactor, admixing in a highly modified polymeric additive into the polymer melt within the slip stream, then introducing the modifier containing slip stream late in the manufacturing process prior to the slip stream withdrawal point. The improved processes of the invention have particular utility for large-scale, continuous reactor where transitions and short production runs are economically prohibitive thereby limiting the product breath. The process is particularly suited for producing a family of copolyesters using a continuous melt phase production process.

The invention discloses a process for synthesizing sucrose polyester, particularly a process for synthesizing sucrose polyester by using a rotating film transesterification flow reactor. The process comprises the following steps: methyl oleate, sucrose powder, potassium stearate and potassium carbonate are added into a mixing kettle, and heated while stirring; the materials enter the rotating film transesterification flow reactor to react; the crude fatty acid sucrose polyester product obtained after the reaction enters a product storage tank, and the reaction product methanol enters a methanol receiver after being cooled by a condenser; and the crude product in the product storage tank is neutralized with acetic acid, washed and dried to obtain the sucrose polyester product. The low-boiling-point substances generated in the process provided by the invention are quickly removed out of the reaction system, thereby being beneficial to the generation of the product, greatly increasing the reaction speed and enhancing the product quality. The process can be used for continuous-feeding production, is beneficial to large-scale production, enhances the production efficiency, has the advantages of high yield and simple process, lowers the production cost and raises the resource utilization ratio.

A method for preparing poly-alpha-olefin in a continuous manner is disclosed and comprises the following steps: introducing alpha-olefin into a continuous reactor in a continuous manner, under the existence conditions of a lewis acid catalyst and an optional cocatalyst, performing polymerization reaction on alpha-olefin, so as to form poly-alpha-olefin, and leading out the material flow containing poly-alpha-olefin out of the reactor. The alpha-olefin is one or more selected from C6-C14 alpha-olefins.

The invention relates to a precursor of a lithium ion battery cathode material, a preparation method thereof, a cathode active material of a lithium ion battery, a lithium ion battery, and a continuous reactor, and belongs to the technical field of new energy materials. The preparation method of the precursor comprises following steps: mixing nickel salt, cobalt salt, manganese salt, doped metal salt (D salt), a precipitating agent, and a complexing agent to obtain a reaction system; carrying out reactions under stirring at a temperature of 30-80 DEG C in an inert gas atmosphere, wherein the pH is 10.0-13.0 during the reaction process, raw materials are fed into the system continuously, and reaction products are discharged continuously through overflowing; and aging the overflowed materials for 1 to 5 hours to obtain the precursor. When the granularity of overflowed materials reaches a set value, the reaction system is subjected to an ultrasonic treatment until the granularity of overflowed materials is lower than the set value. The obtained precursor has the advantages of uniform granularity and morphology, and large tap density, and is benefit for the preparation of a lithium ionbattery cathode material with excellent electrochemical properties.

Disclosed are a concentrate of fine ceria particles for chemical mechanical polishing, and a method of preparing the same. The method includes reacting a reactant mixture comprising i) water, ii) an aqueous solution of water-soluble cerium salt compound, and iii) ammonia or ammonium salt at a reaction temperature of 250-700 ? under a reaction pressure of 180-550 bar for 0.01 sec to 10 min in a continuous reactor to obtain a solution containing the fine ceria particles, the cerium salt compound being contained at an amount of 0.01 to 20 wt % in the reactant mixture; and concentrating the solution containing the fine ceria particles in a concentrator having a filter with a pore size of 0.01 to 10 ?. The concentrate is advantageous in that a CMP slurry and a dispersing solution are easily produced by diluting the concentrate and adding an additive to the concentrate.