844 results about "Residual monomer" patented technology

The present invention provides a highly productive method for manufacturing a water-absorbing resin, the amounts of fine powder and dust of which are small, the amount of residual monomer of which is small, and whose absorption rate is high. That is, the method for manufacturing the water-absorbing resin of the present invention is a method for crosslinking and polymerizing an aqueous solution of an acid-group containing unsaturated monomer, and is characterized in that stationary polymerization is carried out in such a manner that a solid matter is added to the monomer aqueous solution, and an initiation temperature of the polymerization is adjusted to 40° C. or more or a maximum temperature of the polymerization is adjusted to 100° C. or more.

In order to produce inexpensively with high productivity a water-absorbent resin of which: the residual monomer content and the water-extractable content are both low, and the properties are high, and the colorability is low; there is provided a process for producing a water-absorbent resin, which is a process for producing a crosslinked water-absorbent resin by polymerizing a monomer component including acrylic acid and/or its salt in a major proportion wherein the acrylic acid is a product obtained by catalytic gas phase oxidation of propylene and/or propane, with the process being characterized by comprising the steps of: preparing the monomer component from an acrylic acid composition that includes the unneutralized acrylic acid and a methoxyphenol and has a methoxyphenol content of 10 to 160 ppm by weight (based on the unneutralized acrylic acid); and then carrying out radical and/or ultraviolet polymerization of the resultant monomer component.

The present invention relates to high solid content vinyl acetate-ethylene copolymer latex for binder and the synthetic method, including 55 to 75 portion of vinyl acetate, 24 to 45 portion of ethylene, 3 to 5 portion of N-methylol acrylamide, 2 to 4 portion of PVA1788 and PVA0588, 0.4 to 1.0 portion of the compound of nonionic emulsifying agent nonyl phenol polyoxyethylene alkyl ether and anion emulsifying agent alkyl sulphate with 2:1 mixture ratio, 0.2 to 1.0 portion of 35 percents oxydol with 1:1 mixture ratio, 0.05 to 0.4 portion of formol zinc sulphate, 0.1 to 0.5 portion of ferrous sulphate, 0.5 to 1.0 portion of regular dodeca-carbon thiol-alcohol, 0.05 to 0.35 portion of potassium phosphate, 0.1 to 0.5 portion of sodium bicarbonate and 45 to 55 portion of de-ionized water. With the adoption of latex polymerization, low-residual monomer VAE latex with solid content more than 65 percents is synthesized, which is used as binder to be applied in timber processing industry and packaging industry.

A toner suitable for use in electrophotography, etc., is composed of toner particles each containing a binder resin, a colorant and a wax component. Each toner particle has such a microtexture as to provide a cross section as observed through a transmission electron microscope (TEM) exhibiting a matrix of the binder resin, a particle of the wax enclosed with the matrix; and the binder resin dispersed in a particulate form in the wax particle, and the toner particles have a residual monomer content of at most 500 ppm by weight of the toner particles. The colorant may also be dispersed in the wax particle enclosed within the matrix of the binder resin.

A resin to be added to a resist composition and locally distributed on a resist film surface to hydrophobitize the resist film surface includes a residual monomer in an amount of 1 mass % or less to the resin as a whole in terms of solid content.

The present invention provides a process for producing a water-absorbent resin of which the residual monomer content and the extractable content are low. The process for producing a water-absorbent resin comprises the step of polymerizing at least one monomer component including acrylic acid and/or its salt as major components to produce a water-absorbent resin that is a neutralized salt, and this process is characterized in that the acrylic acid is a product obtained by catalytic gas phase oxidation of propylene and/or propane and has a protoanemonin content of not more than 10 ppm, and in that the resultant water-absorbent resin has a neutralization ratio of not less than 50 mol %.

A method for preparing polymer for PAN precursor, by copolymerizing the water phase suspend using ammonium persulphate-ammonium sulfite or ammonium bisulfite as a primosome, is disclosed. The polyacrylonitrile powder material is obtained by adding the first monomer acrylonitrile, the second monomer crylic acid, methyl acrylate or acrylamide, and the third itaconic acid, or the first monomer crylic acid, the second monomer methyl acrylate or itaconic acid, and inorganic oxidation-reduction primosome without any metallic ion which comprises ammonium persulphate, ammonium sulfite or ammonium bisulfite and acidified deionized water into the polymerization kettle in defined proportions, controlling the temperature and stirring to react for a time, and discharging by removing the residual monomer, washing and drying. The average molecular weight is from 17.5 myriads to 26.1 myriads, and the distribution index of molecular weight is from 2.70 to 2.91; the intension of polyacrylonitrile precursor tested by spinning sample is from 4.58 to 6.61 CN/dtex; and the carbon fiber strength is 3.61-5.06MPa.

An adhesive composition comprising at least one tackifier resin and at least one acrylic polymer is provided wherein the tackifier resin comprises monomer repeating units from at least one aromatic monomer and at least one acrylate monomer; and wherein the tackifier resin has a low residual monomer concentration. Processes to produce the adhesive composition is also provided.

The invention relates to a hyper-branched polycarboxylate high-efficiency water reducing agent and a preparation method thereof. The water reducing agent is prepared by polymerizing one of tert-butyl acrylate and methyl tert-butyl acrylate with sodium methyl-acryl sulfonate and allyl polyethenoxy ether to form a copolymer main chain, and then performing condensation polymerization on one of acrylic acid and methacrylic acid with ethylene diamine to form a hyper-branched polyamide structure which is grafted to two ends of the main chain. The preparation method comprises the following steps: (1) preparing the sodium methyl-acryl sulfonate into solution with DMF, and heating the solution in a nitrogen atmosphere; (2) dissolving the other two monomers and an initiating agent into the DMF to prepare mixed solution, and dripping the mixed solution into the step (1) to react for 1 to 20 hours; (3) adding a condensating agent CDI after the reaction and performing condensation reaction by using N-methyl morpholine as an organic base, the ethylene diamine and the acrylic acid as the monomers and the DMF as a solvent; and (4) performing vacuum distillation to remove the residual monomers and the solvent, and refluxing for 2 to 5 hours by using methylene chloride solution of trifluoroacetic acid to obtain the water reducing agent. The hyper-branched polycarboxylate water reducing agent has the advantages of low admixture, high water reducing rate, small slump loss, good compatibility with cement, no corrosivity to steel bars, strong frost resistance and the like.

A polymer polyol comprising 25 to 60 mass % polyol (A) and 40 to 75 mass % of polymer particles (B1) formed by polymerizing ethylenically unsaturated monomer in the polyol (A), the ethylenically unsaturated monomer having the content of acrylonitrile and/or styrene is not less than 50 mass %, wherein (B1) has a particle size of not more than 100 μm and contains not less than 95 mass % of particles with the particle size of 0.01 to 10 μm; and the total content of acrylonitrile and styrene is not more than 20 ppm; and process for producing the polymer polyol. The polymer polyol exhibits a reduced residual monomer content and excellent filtration property and is useful as a raw material in the production of polyurethane or the like.

The invention discloses low-odor low-volatilization modified polypropylene material and a preparation method thereof. The low-odor low-volatilization modified polypropylene material is composed of the following raw materials by weight, polypropylene 65-89%, low-odor low-volatilization absorbent 0.5-3%, inorganic filler 5-15%, polyolefin elastomer (POE) flexibilizer 5-15% and antioxygen 0.1-2%. The low-odor low-volatilization modified polypropylene material has the advantages that nano-zinc oxide which is prepared by a microemulsion method is used for preparing nano-zinc oxide modified active carbon materials and loaded on the surface of multihole active carbon, residual monomers, decomposers and organic acid in base materials of polypropylene are effectively absorbed, obvious effect of absorbing odor is achieved, preparing process is simple, and production cost in low.

Enhanced conversion rates are realized in a suspension polymerization process for styrene through the use of peroxide initiators having one hour half life temperatures from 101° to 111° C. are disclosed. Also disclosed are suitable initiator combinations which provide polymeric products with low residual monomer content at reduced process temperatures, polymerizable compositions containing such initiators and products produced by such processes and compositions.

The invention discloses an acrylic-ester hot-melt pressure-sensitive adhesive and a preparing method thereof. The acrylic-ester hot-melt pressure-sensitive adhesive comprises, by weight, 1-10 parts of hard monomer, 70-95 parts of soft monomer, 1-5 parts of functional monomer, 1-5 parts of polymerizable UV photoinitiator, 0.2-0.5 part of free radical polymerization initiator and 0.01-0.1 part of molecular weight modifier. According to the acrylic-ester hot-melt pressure-sensitive adhesive, storage stability and weather resistance can be improved, the size shrinkage is small during cure crosslinking, coated base material adhesive force is large, adhesive shifting is not prone to occurrence, and the acrylic-ester hot-melt pressure-sensitive adhesive can be widely applied to the food contact field and the medical field. In addition, the body polymerization technology is adopted and is different from the conventional solution polymerization technology and the conventional emulsion polymerization technology, the amount of residual monomer in macromolecule prepolymers is quite small, the content of solid of a polymerization product is 100%, solvent discharging and water volatilization are avoided in the coating process of the pressure-sensitive adhesive, energy consumption is low, and the environment is protected.

The invention discloses a modification method for using low-temperature plasma to initiate gas-phase grafting on the surface of a polyethylene film. The modification method comprises the following steps of: 1) adopting a low-temperature plasma treatment machine with the power being 1KW-20KW and the voltage being 380V to carry out corona treatment on the polyethylene film; 2) after mixing liquid acrylic-acid monomer and an activating agent at the weight ratio being 100: (1-20), vaporizing by a vaporizing chamber with the temperature being 120-200 DEG C, and uniformly spraying on the surface ofthe polyethylene film after corona treatment by a spraying nozzle in a gaseous form; and 3) generating ultraviolet light for irradiation by a high-voltage mercury lamp with the wavelength being 365nmand the power being 500W-5000W, sensitizing the activating agent by the ultraviolet light, initiating the grafting of the acrylic-acid monomer on the surface of the polyethylene film, blowing by hot air with the temperature being 50-80 DEG C, removing the residual monomer and obtaining the polyethylene film with the gas-phase grafted surface. The modification method is high in reaction rate of gas-phase grafting on the surface, is suitable for large-scale continuous production, is lower in cost, the surface tension permanency is improved, and the problem of quality stability of the composite packaging film can be solved.

The invention provides a thermal expansibility microsphere and a method for reducing residual monomers therein. The method comprises a re-initiation step of supplementing an initiating agent of the residual monomers in a process of preparing the thermal expansibility microsphere by using a suspension polymerization method, wherein the initiating agent of the residual monomers is an oxidation reduction initiator system. The preparation method of the thermal expansibility microsphere, provided by the invention comprises the following steps: preparation of a water phase, preparation of an oil phase, suspension polymerization and residual monomer reduction. The technical scheme provided by the invention realizes quick reduction of the residual monomers under a low-temperature condition, is simple in production process, low in consumption and short in processing time, and simultaneously can efficiently reduce the content of the residual monomers in the thermal expansibility microsphere and a suspension reaction medium. The thermal expansibility microsphere prepared by using the method contains a little number of residual monomers and is small in pollution.

The invention relates to a process for the production of post-crosslinkable thermoplastic resins by bulk-polymerizing a polymerizable composition (A) comprising (I) a monomer fluid containing a cyclic olefin (α) having two or more metathetical ring-opening reaction sites in the molecule in an amount 10 wt % or above based on the total amount of the monomers or a monomer fluid containing a norbornene monomer and a crosslinking agent, (II) a metathetical polymerization catalyst, and (III) a chain transfer agent; thermoplastic resins obtained by this process; and a process for producing crosslinked resins or crosslinked resin composite materials which comprises laminating such a thermoplastic resin with a substrate at need and then crosslinking the thermoplastic resin. According to the invention, thermoplastic resins which are free from odor due to residual monomers and excellent in storage stability can be efficiently obtained by a simple process of bulk-polymerizing the composition (A). The process is not only easy and simple but also applicable to continuous production, thus being industrially advantageous. The crosslinked resins and crosslinked resin composite materials obtained according to the invention are excellent in electrical insulation properties, mechanical strengths, heat resistance, dielectric characteristics and so on, thus being useful as electrical materials or the like.

The invention relates to high activity hydroxy terminated polyepichlorohydrin polylol with simple preparation technology and good color, and the preparation method thereof. The high activity hydroxy terminated polyether has the molecular structure including a large quantity of methylene lateral chloro groups and terminated by epoxy ethane or propylene oxide, and the high activity hydroxy terminated polyepichlorohydrin polylol has the average relative molecular mass of 500-9000 and the average hydroxide radical functionality of 2-3. The preparation method comprises the following steps: low molecular mass initiator and dual-metal prussiate complex compound catalyst are added in a pressure-proof reaction kettle, volatile components are removed in a vacuumed mode, part of epoxy chloropropane are added in the low molecular mass initiator and dual-metal prussiate complex compound catalyst, all the reactants are heated to 100-140 DEG to react under the nitrogen protection and the high-speed stirring, and the rest part of epoxy chloropropane is added gradually drop by drop after the activation; after the polymerization reaction is finished, the temperature is reduced to 90-120 DEG C, propylene oxide or epoxy ethane is added drop by drop for end capping, and residual monomer is removed in a vacuumed way after the reaction, thus the hydroxy terminated polyepichlorohydrin polylol is obtained.

The invention provides a styrene acrylic emulsion for interior wall coating material, and a preparation method of the styrene acrylic emulsion; the preparation method comprises the following steps of: (1) mixing water, composite emulsifying agent, acrylate monomer and functional monomer, and emulsifying to obtain pre-emulsified liquid A; (2) adding reactive organic silicon into the pre-emulsified liquid A, and emulsifying to obtain pre-emulsified liquid B; (3) adding mixture of water, composite emulsifying agent, methyl alcohol and sodium bicarbonate into the pre-emulsified liquid A obtained in the step (1), and adding initiator for reaction to obtain seed emulsion C; (4) adding the pre-emulsified liquid B into the seed emulsion C obtained in the step (3), and simultaneously adding initiator water solution into the mixed solution; carrying out heat preservation after dripping, and cooling the emulsion; and (5) removing residual monomer, and adjusting the pH to be 7-8 to obtain the styrene acrylic emulsion for the interior wall coating material. The styrene acrylic emulsion can be used for preparing the interior wall coating material, and is less in adding quantity and better in scrub resistance than that of other emulsions, thus reducing the cost of coating and saving resources.

The present invention relates to water-in-oil polymer dispersions comprising of a continuous organic phase and therein finely dispersed and cross-linked, water-swellable polymerizates, where these have a residual monomer content of less than 1,000 ppm. The present invention relates further to a process for the production of polymer dispersions according to the invention. In addition, the present invention relates to devices for fire prevention and firefighting and to the use of the polymer dispersions according to the invention.