171results about How to "High monomer conversion rate" patented technology

Group 4 metal complexes useful as addition polymerization catalysts of the formula:

wherein

• • G¹ is a group containing from 1 to 40 atoms not counting hydrogen;
  • T is a divalent bridging group of from 10 to 30 atoms not counting hydrogen, selected from mono- or di-aryl-substituted methylene or silylene groups or mono- or di-heteroaryl-substituted methylene or silylene groups, wherein at least one such aryl- or heteroaryl-substituent is substituted in one or both ortho-positions with a secondary or tertiary alkyl-group, a secondary or tertiary heteroalkyl group, a cycloalkyl group, or a heterocycloalkyl group,
  • G² is a C_6-20 heteroaryl group containing Lewis base functionality,
  • M is the Group 4 metal,
  • X″″ is an anionic, neutral or dianionic ligand group,
  • x″″ is a number from 0 to 5, and
  • bonds, optional bonds and electron donative interactions are represented by lines, dotted lines and arrows respectively.

The invention relates to a temperature and salt resistant grafted polyacrylamide synthesized by a macromonomer route, belonging to the research field of water-soluble polymer used for displacement of reservoir oil. A method of chain transfer free radical polymerization and terminal group replacement is adopted to obtain a polyacrylamide (N,N-dimethylacrylamide) type macromonomer. Under an oxidation-reduction complex initiation system, temperature and salt resistant monomers, such as the macromonomer, acrylamide, N-polyvinyl pyrrolidone, N,N-dimethylacrylamide, 2-Acryloylamino-2-methyl propanesulfonic acid and the like, are copolymerized to obtain a target product. From molecular design, a functional long-grafted side chain can increase the viscoelasticity of the polymer molecule and lower solution surface tension. The product provided by the invention can be used for three-class oil deposit and provides a possible solution for improving the recovery ratio for chemical displacement of reservoir oil.

The invention relates to a method for preparing monodisperse polymer microspheres. The method comprises the following process steps: adding a dispersion medium with a stabilizing agent dissolved inside to an impinging stream reactor, heating the dispersion medium, adding a monomer with an initiating agent dissolved inside in one step, carrying out constant-temperature polymerization reaction, obtaining polymer microsphere emulsion after stopping cooling, then using an ultracentrifuge to carry out centrifugal sedimentation, adding absolute ethyl alcohol after removing supernatant, carrying out ultrasonic washing multiple times and drying the washed microspheres to constant weight, thus obtaining the monodisperse polymer microspheres. Compared with the prior art, the method has the following advantages: the prepared polymer microspheres have good apparent morphology, good smoothness and monodispersity and uniform grain sizes; the process is simple to operate; the grain sizes of the microspheres can be well controlled according to the formula; and the grain size range applicability is better.

A liquid laundry detergent formulation is described including a surfactant, a polycarboxylate builder and a 2-methyl-1,3-propanediol carrier solvent. A particularly preferred builder comprises a non-hydrophobically modified, acrylic/polyether comb-branched copolymer, wherein the polyether portion comprises moieties derived from at least two constituents selected from the group consisting of ethylene oxide, propylene oxide, and butylene oxide. Preferably, the comb-branched copolymer is made according to a process selected from the group consisting of: (i) copolymerizing an unsaturated macromonomer with at least one ethylenically unsaturated comonomer selected from the group consisting of carboxylic acids, carboxylic acid salts, hydroxyalkyl esters of carboxylic acids, and carboxylic acid anhydrides, and (ii) reacting a carboxylic acid polymer and a polyether prepared by polymerizing a C2-C4 epoxide, wherein the carboxylic acid polymer and the polyether are reacted under conditions effective to achieve partial cleavage of the polyether and esterification of the polyether and cleavage products thereof by the carboxylic acid polymer.

The invention relates to a water soluble polymer reverse micro emulsion with high solid content and low oil-water ratio, which comprises (1) preparing water-soluble vinyl monomer into 40-70% vinyl monomer water solution, (2) feeding high-purity nitrogen into the mixture of oil phase, emulsifier and stabilizer, mixing completely, increasing temperature to 30-50DEG C, adding vinyl monomer water solution, mixing, synchronously adding inducer and polymerization speed control agent, feeding high-purity nitrogen, reacting for 3-5h to obtain reverse micro emulsion. The prepared reverse micro emulsion has 35-42% solid content and 99.5-100% monomer conversion rate, while the stable storage period is longer than half yield, the product is easily dissolved in water and the application effect is better than the water soluble polymer reverse micro emulsion which oil-water ratio is higher than 1:1.

The invention relates to a device for continuously polymerizing lactide monomer, wherein said device comprises a tubular polymer reactor, a meter pump and a fuser, which are serially connected; the tubular polymer reactor is formed by several serially connected tubular stable mixers whose diameters are increased stepped; the meter and the fuser are serially connected to the small end of reactor. The invention also provides a relative method, which comprises: adding material into the fuser, to be fused and mixed; using meter pump to feed the mixture into the small end of reactor, to pass all stable mixers; the polymer will be extruded from the large end. The invention has high transform rate, high yield and high quality.

The invention relates to a method for preparing a silicone acrylic emulsion with high solid content (of over 50 percent), high organic silicon content (of over 15 percent) and low emulsifier consumption (of less than 2.5 percent), in particular a silicone acrylic emulsion for preparing high-grade exterior wall coating materials. The method comprises steps of preparing a vinyl polysiloxane emulsion by using octamethylcyclotetrasiloxane, tetravinyl tetramethylcyelo tetrasiloxane, dodecylbenzene sulfonic acid, sodium dodecyl benzene sulfonate, a non-ionic emulsifier NP-40 and deionized water through acid catalyzed ring opening, and performing silicone acrylic emulsion copolymerization of the vinyl polysiloxane emulsion and acrylic monomers in the presence of a thermal initiator to prepare the stable silicone acrylic emulsion with high solid content, high organic silicon content and low emulsifier consumption. By the method, problems that the silicon content cannot be improved substantially, the solid content is low and the emulsifier consumption is high in the preparation of the silicone acrylic emulsion are effectively solved. The silicone acrylic emulsion has excellent weather resistance, stain resistance, water resistance and the like, and has high cost performance; and the application range of the silicone acrylic emulsion is greatly widened.

The present invention provides a method of preparing UV-curable inkjet pigment ink for textile printing, in which mini-emulsion techniques are used to encapsulate monomer, photo initiator, thermal initiator and pigment in mini-emulsion particles to make a UV-curable pigment paste, and the UV-curable pigment paste is mixed with water-soluble co-solvent, surfactant and water to make a UV-curable pigment ink. The preparation process is simple and easy. The UV-curable inkjet pigment ink of the invention exhibits good fluency during printing, bright color and strong color fastness in printed products.

A process for semi-continuously preparing organofluorine polymer grafted polyether polyol includes such steps as adding mixed solvent, xylene and methylisobutyl methanone to reactor, adding the monomer mixture liquid including vinyl or acryl ester, unsaturated polyether polyol, AIBN, etc and the organofluorine monomer liquid to reactor, and copolymerizing reaction. The product can be used to prepare F-C paint which features high weatherability and resistance to acid, alkali, chemical corrosion and ultraviolet ray, and high adhesion.

The invention relates to a loop reactor for carrying out continuous polymerization reactions for the production of polymers with adjustable polymer properties comprising a three-dimensional tubular loop comprising at least two tube bends with interposed tube segments, the tube bends having a curving angle of greater than 30°, and the distance between two tube bends being at least three times the tube diameter, the tube bends and the tube segments being arranged in a direction reversed to the curving direction of the tube bends arranging in succession.

The invention relates to methods and systems for the use of an oligomer recyclate from a depolymerization product stream. The oligomer byproduct of a polyester depolymerization reaction can be used as a reactant in the formation of a polyester. For example, linear oligomer byproduct can be used as a reactant in a solution polymerization to form a low-acid polyalkylene terephthalate.

The invention discloses an acrylate/silicone-acrylate compound emulsion and a method for preparing the same. Acrylate emulsions are prepared from acrylate as a main monomer, polyoxyethylene alkyl ether ammonium sulfate as emulsifier and various functional monomers containing carboxyl and are compounded with an silicone-acrylate emulsion to prepare the novel compound emulsion. The process for preparing the compound emulsion is simple, and the compound emulsion not only has the good hydrophobicity, stain resistance, washability and recoatability of the silicone-acrylate emulsion, but also has the good film forming performance, glossiness and solvent resistance of the acrylate emulsion. The compound emulsion film has higher mechanical strength and stronger adhesive force, the problems that the silicone-acrylate emulsion film has lower strength, poor adhesion and the like are solved, and the application range of the silicone-acrylate emulsion film is enlarged. The acrylate/silicone-acrylate compound emulsion can be applied to the field of emulsion coatings for coating roofs, internal walls, external walls, kitchens and the like and also can be applied to the water-proof stain-resistance occasions. The acrylate/silicone-acrylate compound emulsion can improve the grade of the emulsion coating.

A preparation method of small particle-sized polybutadiene latex used for the production of ABS is disclosed, which includes putting components comprising 34.00-45.00% by weight of the butadiene, 0-6.0% by weight of the second monomer, 52.11-63.13% by weight of the desalinized water, 0.12-0.22% by weight of the mercaptan(TDM), 0.80-2.60% by weight of the emulsifiers composed of potassium abietate and potassium oleate, into the same polymerization reactor, then heating the mixture of the components and stirring the same at a temperature range of 60-75° C. The reaction lasts for 9-12 hours and the conversion is higher than 97%. The method has the advantages such as higher conversion, shorter reaction period and lower latex viscosity. During the first stage of the reaction, more heat is released by increasing the reaction rate. When the conversion reaches 40-80%, the heat release rate of intermediate stage is depressed by decreasing the reaction temperature. When the conversion is higher than 80%, the reaction temperature reaches the highest. Thus, severe heat release is avoided. Moreover, the butadiene polymerization can be controlled steadily and the reaction period is shortened.

The invention discloses a superfine environment-friendly thermal expansion microcapsule which is prepared from a suspension dispersing liquid of an oil phase composition and a water phase compositionby a microwave radiation emulsion polymerization method. A particle size of the superfine environment-friendly thermal expansion microcapsule is of a submicron level; and the microcapsule is high in foaming ratio, environment-friendly, nontoxic and applicable to the fields of textile, papermaking, printing ink, engineering plastics and the like. The invention further discloses a preparation methodof the superfine environment-friendly thermal expansion microcapsule. The thermal expansion microcapsule is prepared on a basis of a microwave radiation radical emulsion polymerization technology; and the preparation method is easy and simple to operate, simple in preparation technology and high in production efficiency.

The invention discloses a polycarboxylic acid water reducing agent with narrow molecular weight distribution and a preparation method thereof, belonging to the technical field of slump retaining agentpreparation. The polycarboxylic acid water reducing agent with narrow molecular weight distribution and the preparation method thereof realize that the molecular weight distribution and controllability of the obtained polycarboxylic acid high-efficiency water reducing agent are greatly improved. After propyl polyoxyethylene ether is mixed with a water-soluble initiator and a water-soluble activechain transfer agent, the obtained molecular weight distribution is narrower, and the dispersibility of the product is better. At the same time, sodium methacrylate sulfonate and modified acrylate compounds are added to facilitate improving of the early strength, slump retention, reinforcement and other properties of the prepared polycarboxylic acid water reducing agent; moreover, a heat preservation interlayer with an automatic regulation function is arranged in a reaction kettle, is beneficial to realizing the conversion of heat transfer and cold transfer in the heat preservation interlayer,improving the lifting sensitivity of the temperature in the reaction kettle, eliminating the need for manual temperature regulation, and effectively avoiding the influence on the preparation of the polycarboxylic acid water reducing agent caused by large temperature control difficulty.

The invention provides a composite initiator of a hydrophobic associated polymer and a preparation method of the hydrophobic associated polymer. The composite initiator is prepared from the following raw materials in parts by weight: 1-10 parts of potassium persulfate, 1-10 parts of ammonium persulfate, 0.5-5 parts of dibenzoyl peroxide, 1-10 parts of sodium hydrogen sulfite, 1-10 parts of sodium sulfite, 0.1-1 part of triethanolamine, 0.5-5 parts of urea, 0.5-5 parts of thiourea, 0.05-0.5 part of azodiisobutyronitrile and 0.05-0.5 part of azobis(isobutylamidine hydrochloride). The method comprises the following steps: a sequentially adding disodium ethylenediamine tetraacetate, sodium formate, lauryl sodium sulfate, acrylamide, AMPS-Na and DiC8AM to deionized water under a magnetic stirring condition, and fully stirring evenly; b introducing high-purity nitrogen into a mixed solution obtained from the step a, adding the composite initiator, and polymerizing to obtain hydrophobic associated polymer gel; and c coarsely crushing the hydrophobic associated polymer gel obtained from the step b, adding sodium hydroxide, hydrolyzing, drying in a blast drying oven, drying and crushing to obtain the product.

The invention relates to a method for preparing a DMAEMA based amphiphilic block copolymer through single electron transfer living free radical polymerization. The method comprises the following steps: adding an initiator, a monomer, deionized water and a catalyst into a reactor, filling nitrogen, stirring for 20 min, adding a ligand under the protection of nitrogen, maintaining the nitrogen atmosphere, reacting at 0-90 DEG C for 10-150 min, taking out the catalyst, dewatering and vacuum drying to obtain a target product. The catalyst is a copper wire, and the initiator is active polymethylacrylic acid dimethyl amino ethyl ester; and the monomer is oil soluble acrylate. The preparation method provided by the invention is high in polymerization speed, high in monomer conversion rate (67% can be achieved within 60 min) and narrow in molecular weight distribution (the minimum can be 1.40), and the molecular weight of each segment of the block copolymer is controllable. The preparation method is simple, convenient and easy to realize and is clean and environment-friendly, thereby providing convenience for industrial production.

The invention relates to a preparation method of a lignin grafted copolymer. According to the method, a catalyst and a hydrogen peroxide redox triggering agent are used for preparing a grafted copolymer of lignin and a styrene monomer. By adopting the method, the highest yield of graft copolymerization reaction is 96.6%; the conversion rate of the styrene monomer is 96.3%; the grafting ratio is 59.5%; the grafting degree is 53.7%. The lignin grafted copolymer can be widely used as a thermoplastic large-molecular surface active material.