2424results about How to "Increase polarity" patented technology

Compositions and methods for conferring tolerance to glyphosate in bacteria, plants, plant cells, tissues and seeds are provided. Compositions include novel EPSP synthase enzymes and nucleic acid molecules encoding such enzymes, vectors comprising those nucleic acid molecules, and host cells comprising the vectors. The novel proteins comprise at least one sequence domain selected from the domains provided herein. These sequence domains can be used to identify EPSP synthases with glyphosate resistance activity.

Disclosed is an organic / inorganic composite porous film comprising: (a) a porous substrate having pores; and (b) an active layer formed by coating a surface of the substrate or a part of the pores in the substrate with a mixture of inorganic particles and a binder polymer, wherein the inorganic particles in the active layer are interconnected among themselves and are fixed by the binder polymer, and interstitial volumes among the inorganic particles form a pore structure. A method for manufacturing the same film and an electrochemical device including the same film are also disclosed. An electrochemical device comprising the organic / inorganic composite porous film shows improved safety and quality, simultaneously.

The present invention relates to no-phosphate corrosion and scale inhibitor and its application. The no-phosphate corrosion and scale inhibitor consists of polyaspartic acid and / or polyepoxy succinic acid 10-20 wt%, polymaleic anhydride 20-30 wt%, copolymer of acrylic acid and 2-acrylamido-2-methyl propenyl sulfonic acid 15-20 wt%, zinc salt 3-5 wt%, natural organic high molecular compound 5-12 wt%, molybdate 5-8 wt%, and other components 5-20 wt%. It has excellent corrosion retarding performance, high scale inhibiting performance and environment friendship.

It is intended to easily separate saponins from isoflavones extracted from starting soybeans thereby giving highly pure saponins at a high yield on an industrial scale. Saponins can be highly efficiently separated from isoflavones by performing multistage extraction under mild conditions such that malonyl isoflavone glycoside, from among isoflavones contained in the starting soybeans, is not converted into isoflavone glycoside, acetyl isoflavone glycoside or isoflavone aglycon. Thus, highly pure saponins can be obtained at a high yield on an industrial scale.

A chemical amplifying type positive resist composition, excellent in adhesion to a substrate and good in resist performances and suitable for exposure using a KrF excimer laser, ArF excimer laser, or the like, which comprises a resin having a polymerization unit of 2-alkyl-2-adamantyl (meth)acrylate and a polymerization unit of a monomer selected from 3-hydroxy-1-adamantyl (meth)acrylate and (meth)acrylonitrile, and an acid generator is provided.

A pattern forming method includes (a) coating a substrate with a resist composition including a resin that includes a repeating unit represented by a following general formula (NGH-1), and, by the action of an acid, increases the polarity and decreases the solubility in a negative developing solution; (b) exposing; and (d) developing with a negative developing solution:wherein RNGH1 represents a hydrogen atom or an alkyl group; and RNGH2 to RNGH4 each independently represents a hydrogen atom or a hydroxyl group, provided that at least one of RNGH2 to RNGH4 represents a hydroxyl group.

Disclosed are novel organopolysiloxane compositions that provide good deposition to the surface of fabric and hair. When incorporated in fabric treatment compositions, they provide anti-wrinkle benefit, softness, and anti-static benefit. When incorporated in hair conditioner compositions, they provide conditioning benefit and anti-static benefit.

A serious of nitro heterocyclic derivatives including a structure of formula (I) are provided. In formula (I), P, Q and R1 to R8 are defined in the specification. The derivatives disclosed in the present invention are characterized in inhibiting tubulin polymerization, and treating cancers and other tubulin polymerization-related disorders with a suitable pharmaceutical acceptable carrier.

The invention discloses a method for preparing cycloxylidin, which belongs to the technical field of pesticides preparation. The method comprises the following steps: under nitrogen protection, N-nitroiminoimidazolidine and an organic solvent are added in a reactor, then sodium hydride is added in batches, and the material is heated to the temperature of 50-60 DEG C, chloropropylene oxide is added drop by drop in the reactor, after the reaction product is cooled, chloroform is added, and the product is filtered by diatomite, then evaporative crystallization is carried out, and the crystals can be precipitated, vacuum distillation is carried out on a processed filtrate to obtain a light yellow dense solid, then heat chloroform is used for extraction, and finally heat ethanol or acetone is used for recrystallization to obtain cycloxylidin: 1-(2,3-glycidyl)-N-nitroimidazoline-2-ylamine, wherein the yield is about 83%. The method has the advantages of short reaction time, high yield and green environmental protection, and is more suitable for large-scale industrial production.

The invention discloses a method for preparing 5-hydroxymethylfurfural by solid acid catalysis. The method comprises the following steps of taking lignin residue hydrolyzed by biomass as carrier raw material of solid acid; synthesizing the raw material into solid acid through a two-step way of carbonization and sulfonation, so that the waste material is recycled and the problem of disposal of pollutants is solved. In the dehydration reaction of lignin-based solid acid catalyzed fructose and glucose, the yield of 5-hydroxymethylfurfural can be respectively 84% and 68%; after the dehydration reaction, the lignin-based solid acid is easy to separate and reusable, the acid density of the solid acid can be reduced after being reused five times, and the yield of the 5-hydroxymethylfurfural is still higher than 75%. The method provided by the invention can be used for realizing emission without pollution, and is helpful for realizing environment-friendly producing process of 5-hydroxymethylfurfural.

A pattern forming method includes (a) coating a substrate with a resist composition including a resin that includes a repeating unit represented by a following general formula (NGH-1), and, by the action of an acid, increases the polarity and decreases the solubility in a negative developing solution; (b) exposing; and (d) developing with a negative developing solution:wherein RNGH1 represents a hydrogen atom or an alkyl group; and RNGH2 to RNGH4 each independently represents a hydrogen atom or a hydroxyl group, provided that at least one of RNGH2 to RNGH4 represents a hydroxyl group.

There is provided a composition comprising one or more photoactive compounds and one or more optimization agents. Surprisingly, the composition requires a small amount of optimization agent to efficiently optimize the polarity, critical wavelength, SPF, PFA, Star Rating, photostability, or any combinations thereof, of the composition. Subsequently, an efficient sunscreen composition is achieved.

The present invention is one kind of thick oil demulsifier and its preparation process, and belongs to the field of petrochemical technology. The present invention features that phenol-amine resin as the initial material is block polymerized with epoxy propane ad epoxy ethane under the action of catalyst to obtain stereo netted macromolecular polyether as the thick oil demulsifier. The polyether as the thick oil demulsifier may be further chain expanded for even high demulsifying effect. The thick oil demulsifier can reach the oil-water interface fast to lower the elasticity and viscosity of the interface film, speed the aggregation of liquid drops and demulsify effectively. The thick oil demulsifier has simple preparation process, is suitable for industrial production, and may be used in the efficient dewatering of oil field produced liquid with different water contents.

A high boiling-point solvent, included in a fluorescent color conversion film, suppresses degradation in color conversion characteristic by compensating for a decrease in dielectric constant due to solidification of the matrix system. The fluorescent color conversion film of the present invention includes, in addition to the high boiling point solvent, organic fluorescent dyes, which absorb light in a near ultraviolet to visible light region and emit visible light of a different wavelength, and a matrix resin bearing the organic fluorescent dye. The high boiling point solvent has a boiling point of 150° C. or higher and a vapor pressure of 5 mmHg or lower at the temperature of 20° C. The fluorescent color conversion film is useful in a fluorescent color conversion filter, which itself is useful in light-emitting devices, such as self-emitting multi-colored- or full colored-displays, display panels and backlights.

The invention provides a grinding aid for slag cement. The grinding aid provided by the invention comprises the following components by weight percent: 5-20wt% of alcohol amine compound, 0.1-5wt% of hydroxypropyl methyl cellulose, 5-30wt% of polyhydric alcohol compound, 0.5-10wt% of sodium hexametaphosphate, 1-10wt% of soluble sulfate, 1-8wt% of sodium dodecyl benzene sulfonate and the balance of water. In the grinding agent provided by the invention, the hydroxypropyl methyl cellulose is beneficial for stimulating the activity of the slag, forming stable hydrous products in the reaction process, improving the property of the cement, improving the strength of the cement and improving the stability of the liquid grinding aid at the same time. Experimental result shows that the grinding aid is capable of increasing the breaking strength of the cement to 9.5MPa and increasing the compressive strength to about 55MPa.

The use of lithium bis(oxalate)borate (LiBOB) as an additive in a lithium secondary battery provides improved battery performance such as long life and high capacity retention after high temperature storage.

The invention provides a preparation method of a semi-interpenetrating network polymer gel electrolyte membrane. The method comprises the following steps: (A) adding a linear polymer and a solvent to a sample bottle, stirring and dissolving the linear polymer and the solvent, adding polyethylene glycol dimethyl acrylic ester, vinylene carbonate and a photoinitiator, and mixing the polyethylene glycol dimethyl acrylic ester, the vinylene carbonate and the photoinitiator evenly to form a solution; (B) coating a glass plate with the solution, covering a layer of glass plate to form a sandwich structure, and curing the sandwich structure to obtain an ultraviolet-cured semi-interpenetrating network polymer membrane; and (C) immersing the ultraviolet-cured semi-interpenetrating network polymer membrane into liquid electrolyte. According to the gel electrolyte provided by the invention, the balance between the ionic conductivity and the mechanical property is relatively well realized; the ionic conductivity at room temperature can be up to 1.49*10<-3>S cm<-1>; the mechanical property is good; the heat stability is good; the electrolyte can be prevented from leaking; the interface stability is good; and a lithium iron phosphate / metal lithium battery assembled by the gel polymer electrolyte membrane has excellent cycle performance and rate performance.

The invention relates to a method for preparing a formaldehyde scavenging agent. The method comprises the following steps of: preparing raw materials such as natural mineral micro powder, water, a binder and amino acid in a mass ratio of 100:(50-1,000):(0.5-5):(1-20), wherein the particle size of the natural mineral micro powder is 0.3 to 5mm; mixing and stirring the natural mineral micro powder and the water at the temperature of between 15 and 30 DEG C for 1 to 3 hours to form suspension; adding the binder, and mixing and stirring at the temperature of between 15 and 30 DEG C for 0.5 to 2 hours to form suspension; adding the amino acid, and mixing and stirring at the temperature of between 15 and 30 DEG C for 0.5 to 1 hour to form suspension; feeding into a spray dryer, and preparing dry porous spherical particle fine powder at the temperature of between 80 and 250 DEG C; and putting the fine powder into a packaging bag, and sealing. The raw materials are cheap and readily available, efficiency is high, energy consumption is low, and the prepared formaldehyde scavenging agent is high in adsorption capacity and long in action time.

The invention discloses a polar monomer graft-modified amorphous poly-alpha-olefin and a preparation method thereof. The polar monomer graft-modified amorphous poly-alpha-olefin is prepared by carrying out grafting reaction on amorphous poly-alpha-olefin, a peroxide initiator, a polar monomer and an auxiliary grafting agent under molten or dissolved conditions. The polar monomer graft-modified amorphous poly-alpha-olefin is prepared from the following raw materials: 100 parts of amorphous poly-alpha-olefin, peroxide initiator accounting for 0.1-1 wt% of the amorphous poly-alpha-olefin, polar monomer accounting for 0.5-10 wt% of the amorphous poly-alpha-olefin, auxiliary grafting agent accounting for 0.1-5 wt% of the amorphous poly-alpha-olefin, solvent accounting for 0-300 wt% of the amorphous poly-alpha-olefin, and antioxidant accounting for 0.05-2 wt% of the amorphous poly-alpha-olefin. The amorphous poly-alpha-olefin has the characteristics of high grafting ratio, light color, high polarity, favorable flowability, favorable storage capability and no risk in moisture crosslinking.

The present invention relates to high nitrogen doped corrugated carbon nanotube material and its synthesis process. The synthesis process includes the following steps: mixing Fe source and proper amount of distilled water, soaking porous molecular sieve to carry ferric oxide or ferrous oxide, stoving and roasting at 300-1000 deg.c for 0.5-24 hr to obtain catalyst; setting the catalyst inside a pipe furnace, leading organic amine into the furnace under the protection of Ar or N2 and reacting at 650-1000 deg.c for 0.2-4.0 hr to obtain high nitrogen doped corrugated carbon nanotube mixture containing the catalyst; soaking the mixture in proper amount of or excessive hydrofluoric acid, sulfuric acid, nitric acid or acid for 0.5-24 hr; and washing in distilled water, suction filtering and drying to obtain high nitrogen doped corrugated carbon nanotube material. The material has nitrogen content of 10-40 %, reinforced surface polarity, etc, and is suitable for industrial production.

Improved synthesis of seco(−)CBI (5-hydroxy-3-amino-1-[S]-(chloromethyl)-1,2-dihydro-3H-benz(e)indole):and improved syntheses therefrom of a wide variety of CC-1065 analogs that comprise a cyclopropabenzidole (CBI) alkylating moiety, and which are collectively DC1 and its derivatives, for the synthesis of cell-targeted therapeutic agents.

The invention discloses a solvent-free polyurethane adhesive for a flexible package, which is prepared by at least mixing a component A and a component B, wherein the component A is an endcapped polyurethane prepolymer containing terminal isocyanate groups, and the B component is a combination which is formed by compounding polyether polyol and polyester polyol of liquid styrene butadiene rubber containing terminal hydroxy groups and / or liquid acrylonitrile butadiene rubber containing terminal carboxyl groups. The solvent-free polyurethane adhesive of the invention is suitable for solvent-free compounding of the flexible package and has the advantages of low cost, wide compound substrate range (substrates such as plastic films, aluminum-coated films, aluminum foil and the like can be compounded), high bonding strength (the peeling strength of BOPP / PE reaches more than 4N / 15mm, the peeling strength of PET / VMPET reaches more than 4.5N / 15mm, and the peeling strength of the inner film of PET / AL / PE reaches more than 6N / 15mm), wide application temperature range (25-55 DEG C), long service life of a plastic plate (the service life is longer than 40 minutes when the plastic plate is used at 50 DEG C), good leveling property, no solvent discharge, environmental friendliness and the like.

The invention provides a process for making hollow microparticles. The process comprises providing a dispersion having a continuous aqueous phase and a discontinuous organic phase and polymerising a monomer in the dispersion to form hollow polymeric microparticles. The continuous aqueous phase of the dispersion comprises a stabiliser and the discontinuous organic phase of the dispersion comprises the monomer and an organic liquid. The monomer has two or more polymerisable groups per molecule. Prior to the step of polymerising the monomer, the discontinuous organic phase does not contain a polymer.

The invention provides an ink-jet recording material and a preparation method thereof as well as a method for preparing an ink absorption layer coating liquid, and relates to an ink-jet material and a preparation method thereof as well as a method for preparing an ink absorption layer coating liquid, so that the problems of poor ink absorption effect, nonuniform color distribution of printed images, unclear printed images and higher preparation cost of the existing ink-jet recording material can be solved. The ink-jet recording material is prepared from the ink-jet layer coating liquid which is prepared from PVC (polyvinyl chloride) serving as a base material, a 20-30% polyacrylic acid emulsion serving as a primer, an inorganic nano-pigment with the thickness of 10-100nm, a dispersing agent, acetic acid, deionized water and an adhesive aqueous solution. The prepared ink-jet recording material prepared through PVC material corona treatment, PVC substrate glue coating, drying, ink absorption layer coating and drying has the advantages that that the printed image is clear, the ink droplet does not diffuse, and the color is distributed uniformly; and the ink-jet recording material has excellent performances of color definition, color saturation, glossiness and the like. The raw material cost and the manufacture cost are low, so the ink-jet recording material is advantageous to industrial production, popularization and application.