6048 results about "Pyrrolidinones" patented technology

The invention relates to the preparation of a hydrogel surface useful in the formation and manipulation of arrays of molecules, particularly polynucleotides and to the chemical modification of these and other arrays. In particular, the invention relates to a method of preparing a hydrogel immobilised to a solid support comprising polymerising on the support a mixture of a first comonomer which is acrylamide, methacrylamide, hydroxyethyl methacrylate or N-vinyl pyrrolidinone and a second comonomer which is a functionalised acrylamide or acrylate.

The invention relates to novel crosslinkable copolymers which are obtainable by (a) copolymerizing at least two different hydrophilic monomers selected from the group consisting of N,N-dimethyl acrylamide (DMA), 2-hydroxyethyl acrylate (HEA), glycidyl methacrylate (GMA), N-vinylpyrrolidone (NVP), acrylic acid (AA) and a C₁-C₄-alkoxy polyethylene glycol (meth)acrylate having a weight average molecular weight of from 200 to 1500, and at least one crosslinker comprising two or more ethylenically unsaturated double bonds in the presence of a chain transfer agent having a functional group; and (b) reacting one or more functional groups of the resulting copolymer with an organic compound having an ethylenically unsaturated group.

Processes for the production of metal nanoparticles. In one aspect, the invention is to a process comprising the steps of mixing a heated first solution comprising a base and/or a reducing agent (e.g., a non-polyol reducing agent), a polyol, and a polymer of vinyl pyrrolidone with a second solution comprising a metal precursor that is capable of being reduced to a metal by the polyol. In another aspect, the invention is to a process that includes the steps of heating a powder of a polymer of vinyl pyrrolidone; forming a first solution comprising the powder and a polyol; and mixing the first solution with a second solution comprising a metal precursor capable of being reduced to a metal by the polyol.

The present invention provides an assembly for the preparation of a medical device having a porous coating comprising hydrogen peroxide. Particularly interesting medical devices are catheters (such as urinary catheters), endoscopes, laryngoscopes, tubes for feeding, tubes for drainage, guide wires, condoms, urisheaths, barrier coatings e.g. for gloves, stents and other implants, extra corporeal blood conduits, membranes e.g. for dialysis, blood filters, devices for circulatory assistance, dressings for wound care, and ostomy bags. The coating is in particular a hydrophilic coating formed from cross-linked polyvinylpyrrolidone. In one embodiment, the assembly holds a dry catheter element in one compartment of a package and an aqueous hydrogen peroxide solution in another compartment. The solution may also comprise stabilizers, e.g. chelators, and osmolality increasing agents. The catheter for insertion in the urethra is useful for the treatment, alleviation or prophylaxis of microbial infections such as urinary tract infections (UTI).

The invention discloses high-performance environment-friendly type water-borne polyurethane. The high-performance environment-friendly type water-borne polyurethane is mainly prepared from the following materials in parts by weight: 80-100 parts of polyester polyol, 20-56 parts of aliphatic diisocyanate, 3.5-10 parts of hydrophilic chain extender, 0-8 parts of micromolecule chain extender, 0.01-0.05 part of environment-friendly type catalyst, 5-30 parts of solvent with a low boiling point, 3-12 parts of neutralizer, 0-10 parts of post chain extender and 160-400 parts of deionized water. The invention further discloses a preparation method of the polyurethane. The polyurethane is free of toxic and harmful substances including an organic tin catalyst, N-methylpyrrolidone, a solvent with a high boiling point and the like, capable of satisfying the requirements of latest EU environmental standard rules, anti-yellowing, extremely good in water and heat resistance, good in adhesion resistant adhesion, strong in storage stability, good in gloss, high in solid content and excellent in comprehensive performance.

The invention discloses preparation and application of magnetic nano-composite material gamma-Fe2O3/PDA (Polydopamine)-GA (Gallic Acid). The preparation comprises the following steps of carrying out a hydrothermal reaction and calcinations to obtain a gamma-Fe2O3 nano particle carrier by taking FeCl3.6H2O with low price as an iron source, ethylene glycol (EG) as a reducing agent, polyvinylpyrrolidone (PVP) as a dispersing agent and a protective agent, and natrium aceticum (NaAc) as an alkali source; then wrapping a layer of polydopamine (PDA) in a buffer solution of tris (hydroxymethyl) aminomethane-hydrochloric acid (Tris-HCl) with pH of 8.5; and finally introducing gallic acid (GA) to an ethanol system by using 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride and n-hydroxysuccinimide as cross-linking agents, wherein a specific synthetic schematic diagram is seen in attached drawing 1. Then the adsorption effects of the synthesized magnetic nano-particle on metal ions Cu<2+> and Pb<2+> are discussed, the detection effects of a glassy carbon electrode modified by the magnetic nano-particle on the metal ions Cu<2+> and Pb<2+> are researched. Results show that gamma-Fe2O3/PDA-GA has excellent detection and adsorption effects on heavy metal ions in a water environment.

The invention discloses preparation method of lithium ion battery positive pole size. The preparation method comprises the following steps: firstly mixing polyvinylidene fluoride and N-methyl pyrrolidone to prepare glue solution; mixing a relatively thick mixture of N-methyl pyrrolidone, a carbon nano tube, graphene and conductive carbon black at a high speed and dispersing to obtain conductive agent size; adding lithium iron phosphate and a certain amount of N-methyl pyrrolidone for twice to obtain a relatively thick mixture to mix at a high speed; and adding the N-methyl pyrrolidone to mix at a high speed, adding the glue solution to mix; and finally adjusting the viscosity and screening to obtain the lithium ion battery positive pole size which is good in performance.

The invention discloses a method for preparing poly(arylene ether nitrile) resin powder, and belongs to the technical field of high polymer materials. 2,6-dichlorobenzonitrile and aromatic dihydric phenol are taken as raw materials, 1-methyl-2-Pyrrolidinone is taken as a solvent, anhydrous potassium carbonate or anhydrous sodium carbonate is taken as a catalyst, and methylbenzene or dimethylbenzene is taken as a dehydrating agent; and the method comprises the following steps of: performing reflux reaction at the temperature of between 130 and 160 DEG C for 2 to 4 hours in a reactor, slowly evaporating out water and the dehydrating agent, and raising the temperature to 180-200 DEG C until a macromolecular rod-climbing phenomenon happens; adding the solvent into the reactor, and diluting the reaction products to the mass concentration of 2 to 15 percent; and adding a precipitator into the reactor, continuously stirring, performing centrifugal solid-liquid separation, washing the solid in acidic boiling water, filtering and drying to obtain the poly(arylene ether nitrile) resin powder. The prepared poly(arylene ether nitrile) resin powder has the characteristics of superfine granularity (reaching 100-400 meshes), uniform granularity, high purity, stable performance, and excellent electrical property, and can be widely applied in the fields such as electronics, precision machines, aerospace, new energy and the like.

The present invention relates to aqueous polyurethane dispersions that are free from N-methylpyrrolidone and other solvents and wherein the polyurethanes are the reaction products of A) a mixture of 25% to 90% by weight of 1-isocyanate-3,3,5,-trimethyl-5-isocyanatomethylcyclohexane (IPDI) and 10% to 75% by weight of 4,4′-diisocyanatodicyclohexylmethane, wherein the preceding percentages are based on the weight of component A), with B) one or more polyols having average molarcular weights (Mn) of 500 to 6000, C) one or more compounds which have at least one OH— or NH-functional group and contain a carboxyl and/or carboxylate group, wherein at least 50 mol % of the acid groups, based on the total moles of acid incorporated into the polyurethane, are incorporated by dimethylolpropionic acid, D) one or more polyols and/or polyamines having average molecular weights (Mn) of below 500, and E) optionally one or more monoalcohols and/or monoamines. The present invention also relates to a process for preparing the aqueous polyurethane dispersions and to the use of the polyurethane dispersions for preparing coatings or adhesives.

A purified cannabidiol (CBD) extract and/or cannabidiolic acid (CBDA) extract is isolated from industrial hemp and comprises less than 0.5 wt % organic impurities as measured by HPLC and ¹H NMR spectroscopy exhibits no detectable peak at 4.07 ppm as measured by ¹H NMR spectroscopy. The CBD and/or CBDA extract is in crystalline form. The CBD extract exhibits a melting point as measured by differential scanning calorimetry (DSC) of 69-70° C. Dry powder compositions comprise such extracts. Additional dry powder compositions comprise polyvinylpyrrolidone and an amorphous CBD extract. An adduct comprises CBD and/or CBDA bonded to a paramagnetic trivalent lanthanide (III) metal chelate.

The invention relates to a blocking remover of a gas well shaft. The blocking remover comprises, by weight, 5-25% of an alcohol ether compound, 0.5-10% of a dispersant, 1-10% of a cleaning agent, and 0.5-5% of chelating agent, with the balance being a nitrogen-containing polar solvent, wherein the nitrogen-containing polar solvent is one selected from N,N dimethyl formamide, N,N dimethyl acetamide, and N-methyl pyrrolidone, the alcohol ether compound is one selected from glycol-ether, glycol-propyl ether, glycol-butyl ether, and diglycol-ether, the disperant whose micelle particle size is from 20nm to 100nm is a middle-phase microemulsion-type dispersant mixed by kerosene, water, a surfactant and a cosurfactant, the cleaning agent is one selected from allene diamine, acetonitrile and pentylamine, and the chelating agent is one selected from sodium citrate and EDTA. The blocking remover has the advantages that corrosivity is weak, that the speed of dissolving blockage is fast, that the product performance is stable in high temperatures, and that the blocking remover can reduce damages caused by water locking and fouling in areas close to gas wells, and can recover the permeability of storing layers.

The invention relates to a preparation method of cerium oxide nanoballs, and belongs to the technical field of the preparation processes of the inorganic nanomaterials. The key points of the method of the invention include: stirring and mixing cerium salt and a certain amount of surfactant at room temperature, dissolving the mixture in a mixed solution of water and an organic solvent and ultrasonically processing the mixture for 5 to 10 minutes, wherein the cerium salt is optimally cerium nitrate; the surfactant is most preferably polyvinylpyrrolidone; and the belonged organic solvent is most preferably diglycol; then transferring the mixed solution into a high pressure reaction kettle to perform a solvothermal reaction; heating the mixed solution to perform reaction for 24 to 28 hours at the temperature of 100 to 200 DEG C so as to obtain the cerium oxide nanoball sol; evaporating the sol at the temperature of 1500 o 180 DEG C to dryness; and forging the obtained powder for 1 to 4 hours at the temperature of 400 to 600 DEG C; and finally obtaining the cerium oxide nanoballs in the shape of yellow solid powder. The nanoballs have a particle size ranging from 30 to 160nm and high performance and can be applied in fields of ultraviolet light shielding, mechanical polishing and automobile exhaust catalyzation and the like.

The invention relates to a multicomponent copolymerization oil well cement fluid loss additive and a preparation method thereof. The method comprises: 10-120 portions of 2-acrylamide-2-methyl-1-AMPSA, 1-5 portions of acrylic acid and 15-50 portions of deionized water are added, stirred and then added with sodium hydroxide aqueous solution with the mass fraction of 5-10 percent for neutralizing to pH equal to 3-11; then 10 portions of acrylamide, 0.1-1 portion of complexing agent EDTA and 0.01-1 portion of chain transfer agent are added, the chain transfer agent is isopropyl alcohol or sodium benzoate, the temperature is controlled between 30 DEG C and 60 DEG C and N2 is introduced for 30 minutes; 2-10 portions of N-vinyl pyrrolidone and 0.01-0.5 portion of initiator are added, the initiator is potassium persulfate or ammonium persulfate, and the reaction is carried out for 4-12 hours. The solution keeps still for 5 hours at the temperature of 180 DEG C, and is cooled through flowing water after being taken out, without sedimentation or water separating; and the water loss is zero at the temperature of 180 DEG C according to the standards of drilling fluid, and the water loss is 48ml according to the standards of cement.

The present invention relates to an aligning agent for liquid crystal containing at least a polymer and solvent selected from polyamic acid and polyimide gained by dewatering closed-loop, the solvent contains: (A) a first solvent containing compound with formula (I); (B) a second solvent selected from at least one of N-methyl-2-pyrrolidone, gamma-butyrolactone, 1,3-dimethyl-2-imidazolone, N, N-dimethylformamide and N, N- dimethylacetylamide; and (C) a third solvent selected from at least one of butyl cellosolve, diacetone alcohol, carbonic sub-propyl ester, diethylene glycol diethyl aether and ethyl-3- oxethyl propionic ether. (In formula (I) the R respectively represents alkyl with 3 to 10 carbon atoms).

The invention discloses a preparation method of a modified graphene aqueous dispersion. The preparation method comprises the following steps: preparing graphene oxide slurry and cleaning the graphene oxide slurry to be neutral; covalently modifying by virtue of surfactants such as polyvinylpyrrolidone, polyoxyethylene and sodium polystyrenesulfonate; then, obtaining graphene which is covalently modified by surfactants such as polyvinylpyrrolidone in one step by means of a reducing action; and carrying out ultrasonic dispersion to obtain the modified graphene aqueous dispersion. The modified graphene aqueous dispersion disclosed by the invention is high in stability, good in dispersibility, low in production cost and simple in process. The required equipment is simple, the yield is high and industrialized production is easy to realize.

The invention relates to a self-lubricating wear-resistant coating swash plate, which consists of a metallic matrix and a self-lubricating wear-resistant coating, wherein annular planes on two sides of the metallic matrix are coated with the self-lubricating wear-resistant coating, and the components of the self-lubricating wear-resistant coating comprise a main material of high molecular materials, fluoroplastics, solid lubricants and inorganic matters. A process for producing the self-lubricating wear-resistant coating swash plate comprises that: the self-lubricating wear-resistant coating is coated on the swash plate after being prepared into a liquid coating, and a method for preparing the liquid coating comprises the steps of using a solvent of N-methyl pyrrolidone or dimethyl acetamide to dissolve the main material of the high molecular materials first, and then adding the fluoroplastics, the solid lubricants and the inorganic matters into the mixture to perform sufficient stirring and dispersion so as to prepare the liquid coating with certain solid content. The swash plate has the advantages of good self-lubricating and wear-resistant performance, simple production process and low production cost, and does not contain metallic lead which is harmful to human bodies and the environment.

Photostable cosmetic compositions contain, formulated into a cosmetically acceptable vehicle, at least one UV-screening system that includes:

• • (a) at least one dibenzoylmethane compound, and
  • (b) at least one 2-pyrrolidinone-4-carboxy ester compound having the following formula (I):

in which:

• • R¹ is a linear or branched C₁-C₂₀ alkyl radical, and
  • R² is a linear or branched C₁-C₂₀ alkyl radical which optionally includes a C₅-C₆ ring member, the phenyl radical, the benzyl radical or the phenethyl radical.

The invention relates to a gold nucleus and silver shell double-metal nanocrystal and a preparation method thereof. The crystal is in a rod-shaped structure with a regular crystalline form, wherein the rod-shaped structure is focused on a {100} surface and comprises a double-cube triangle, a cube and a five-twin crystal section, and simultaneously the side surface of the rod-shaped structure is a {100} type crystal surface. The preparation method comprises the following steps of: heating a polyhydroxy-alcohol solution containing chloroauric acid, polyvinylpyrrolidone and silver nitrate, cooling at a room temperature and carrying out centrifugal precipitation to obtain a gold crystal seed; and adding the gold crystal seed obtained by centrifugal separation to a polyhydroxy-alcohol solution containing the polyvinylpyrrolidone, adding the silver nitrate in a molar ratio [AgNO3]/[HuAuCl4], heating by using an oil bath to obtain a product solution, and then carrying out centrifugation to obtain a product. In the first step of reaction in the preparation method, a certain trace of silver nitrate is added to the solution so that the shape of a gold nucleus is effectively controlled, the crystal with a regular crystalline form is obtained, and the shape of a silver shell is finally decided on the shape of the gold seed. The preparation method realizes rapid and batch controllable preparation of a silver-coated gold nano nucleus/silver structure crystal forced on the {100} surface.