4026 results about "Ethylenediamine" patented technology

The invention belongs to the technical field of preparation of a carbon nano material, and particularly relates to a method for preparing a carbon dot having a high fluorescent quantum yield from citric acid and different nitrogen-containing molecules. The method comprises the following steps: weighing 1-10 mmol of solid citric acid, and dissolving in 10 ml of deionized water; weighing 1-10 mmol of ethylenediamine, ethylamine, propylamine, butanediamine, n-hexylamine, p-phenylene diamine or urea, adding into the citric acid solution, and uniformly stirring; transferring the solution into a hydrothermal or high-pressure microwave reaction kettle, reacting under hydrothermal or microwave conditions, and naturally cooling the reaction kettle to room temperature, thus obtaining a yellow or brown carbon dot water solution; and finally, purifying the carbon dot water solution, evaporating, and drying to obtain pure carbon dot solid powder. The carbon dot solution can send out bright blue fluorescence under the irradiation of a handheld ultraviolet lamp. The invention has wide application prospects in the fields of biological imaging, fluorescent printing and the like.

A resin composition is prepared by reacting components comprising dibasic acid, diamine, polyol and monoalcohol, wherein (a) at least 50 equivalent percent of the dibasic acid comprises polymerized fatty acid; (b) at least 50 equivalent percent of the diamine comprises ethylene diamine; (c) 10-60 equivalent percent of the total of the hydroxyl and amine equivalents provided by diamine, polyol and monoalcohol are provided by monoalcohol; and (d) no more than 50 equivalent percent of the total of the hydroxyl and amine equivalents provided by diamine, polyol and monoalcohol are provided by polyol. This resin composition may be formulated into, for example, personal care products, fragrance releasing products and candles.

This invention relates to substrates for use in immobilizing biomolecules. More particularly, the invention relates to substrates (e.g. glass slides) having a coating of polylysine covalently attached to a silane layer coating the slide, wherein the polylysine compound has a functional NH2 group which can be coupled directly, indirectly, covalently, or non-covalently to a biomolecule (e.g., a DNA or RNA molecule). Even more particularly, the invention relates to specific prescribed addition of ethanalomine to the polylysine thereby forming a mixture which dramatically enhances the effectiveness of the polylysine for immobilizing DNA. Among other applications, the polylysine coated substrates can be used in the preparation of high density arrays for performing hybridization assays

The present invention relates to heavy metal chelate compositions, which are used as fungicides and bactericides, and methods of using the compositions. In particular, the present invention relates to a chelate, that is an EDDHA (copper-ethylenediamine-di-o-hydroxyphenylacetic acid), combined with a heavy metal, including iron, tin, zinc, manganese, copper, and combinations thereof.

An aqueous hard surface cleaner with improved soil removal is provided and has, as components, the following:(a) either an anionic, nonionic, amphoteric surfactant, and mixtures thereof with optionally, a quaternary ammonium surfactant, the total amount of the surfactants being present in a cleaning effective amount;(b) at least one water-soluble or dispersible organic solvent having a vapor pressure of at least 0.001 mm Hg at 25° C., present in a solubilizing-or dispersion-effective amount;(c) Tetrapotassium ethylenediamine-tetraacetate (potassium EDTA) as a chelating agent, present in an amount effective to enhance soil removal in said cleaner; and(d) the remainder, water.

The invention provides a method for preparing ethylenediamine from reactants of glycol and ammonia in the presence of a solid catalyst with a main component of copper through a hydrogenation and amination one-step method. The method comprises the following steps of: making glycol containing water or not containing water and ammonia enter a reactor filled with the catalyst with a main component of copper, performing dehydrogenation to obtain the ethylenediamine and water and an ethanolamine byproduct, and separating the mixture obtained through reaction to obtain the product of ethylenediamine.

The invention provides a solid catalyst for preparing ethylene diamine through catalytic amination of ethylene glycol. The catalyst takes copper and nickel as main components and zirconium as an auxiliary component; and other metal components can be one or more than one of zinc, aluminum, titanium, manganese and cerium. The invention further provides a preparation method of the solid catalyst. The preparation method is characterized in that the catalyst is prepared through the processes of roasting, reducing and re-roasting by utilizing a coprecipitation method.

The invention discloses a preparing method of a graphene/waterborne polyurethane composite material. The preparing method is characterized in that firstly, a graphene oxide aqueous dispersion is prepared by an improved Hummers method; then, modified graphene oxide is reduced through ethylenediamine so as to obtain a modified graphene aqueous dispersion; a linear polyurethane prepolymer is synthesized by diisocyanate, a dihydric alcohol oligomer and a chain extender; finally, a neutralizer is added into the linear polyurethane prepolymer for neutralization, and the product is mixed with the modified graphene aqueous dispersion so as to obtain the graphene/waterborne polyurethane composite material. The compatibility of two components in the prepared graphene/waterborne polyurethane composite material is good, and the thermostability and the mechanical strength of waterborne polyurethane are improved through graphene modification. The graphene/waterborne polyurethane composite material can be used as an environment-friendly waterborne paint and has a wide application prospect.

A first variant of an adhesive composition for making a lignocellulosic composite includes soy protein and/or lignin; at least one substantially formaldehyde-free curing agent that includes at least one amine, amide, imine, imide, or nitrogen-containing heterocyclic functional group that can react with at least one functional group of the soy protein; and at least one compound selected from a boron compound, a group IA oxide or hydroxide, or a group IIA oxide or hydroxide. A second variant of an adhesive composition includes a first component selected from soy protein and/or lignin; and at least one substantially formaldehyde-free curing agent selected from a reaction product of epichlorohydrin with ethylenediamine, a reaction product of epichlorohydrin with bis-hexamethylenetriamine, or a reaction product of epichlorohydrin with hexamethylenediamine.

The present invention provides a method for manufacturing polycarbonate, which has a high conversion rate of a propylene oxide material into a polymer and can control stereoregularity of the macromolecular structure, and a catalytic compound for the manufacturing method.

The manufacturing method of the present invention is a method for manufacturing a polycarbonate copolymer by copolymerizing an epoxide compound as a monomer with carbon dioxide in the presence of a planar tetracoordinate-type cobalt-Schiff base complex, wherein a ligand of the Schiff base is N,N′-bis(2-hydroxybenzylidene)ethylenediamine, N,N′-bis(2-hydroxybenzylidene)phenylenediamine, or a derivative thereof, and a methyl group substituted with an amino group having an asymmetrical carbon atom or an asymmetrical axis is introduced to the 3- and/or 3′-position of the benzene ring derived from the salicyl group. In addition, the catalytic compound of the present invention is a cobalt-Schiff base complex, wherein a methyl group substituted with an amino group having an asymmetrical carbon atom or an asymmetrical axis is introduced to the 3- and/or 3′-position of the salicyl group.

Compositions and methods for modulating injection site pain associated with rapid acting injectable insulin formulations have been developed for subcutaneous injection. The formulations contain insulin in combination with a zinc chelator such as ethylenediaminetetraacetic acid (“EDTA”), a dissolution/stabilization agent such as citric acid, a magnesium salt, and, optionally, additional excipients. New presentations include rapid acting concentrated insulin formulations and a way to enhance the absorption of commercially available rapid acting analog formulations by mixing them with a vial containing dry powder excipients that accelerate their absorption. Devices for mixing excipient and insulin together at the time of administration, while minimizing residence time of the mixture, are also described.

The invention discloses a Dendrobium officinale culture solution and belongs to the technical field of agricultural planting. The culture solution comprises the following ingredients: potassium nitrate, ammonium nitrate, magnesium sulfate, manganese sulfate, zinc sulfate, monopotassium phosphate, copper sulfate, potassium iodide, cobalt dichloride, boric acid, sodium molybdate, vitamin VB1, vitamin VB6, vitamin VB5, glycine, ferrous sulfate, disodium ethylenediamine tetraacetic acid, calcium chloride, naphthylacetic acid, mashed banana, mashed potato, white sugar, inositol, and powdered agar. The dendrobium officinale culture solution is reasonable in compatibility, can provide comprehensive nutrition for a Dendrobium officinale stem, fast promote the stem to grow out of a root, increase the polysaccharide content and the amino acid content in the Dendrobium officinale, shorten the time for culturing the Dendrobium officinale stem to a complete plant to about 25 days, and significantly improve the transplanting survival rate of the Dendrobium officinale.

The present invention relates to flue gas purifying treatment technology. The equipment consists of chemical compounding tank with stirrer, chemical adding pump, adsorber tower, circulating pump, storing pond for concentrated absorbent liquid, evaporating inlet pump, evaporator, drying inlet pump and drying machine connected via pipeline. It desulfurizes and denitrificates simultaneously through the mixed reaction of flue gas and absorbent liquid in the absorber tower with urea as absorbent and organic amine or phosphate as additive. It has an SO2 eliminating rate up to 95% and NOx eliminating rate up to 80%, with the recovered ammonium sulfate being used as fertilizer.

The invention discloses a polyamide and amine hybridized nanosilicon dioxide hyperbranched polymer and a preparation method thereof. The preparation method of the polymer comprises the following steps of firstly, modifying the surface of nanosilicon dioxide by using a coupling agent; then, carrying out Michael addition reaction and amidation reaction on the modified nanosilicon dioxide by using ethylenediamine and methyl acrylate; finally, carrying out functional modification by using allyl glycidyl ether to obtain a functional polyamide and amine hybridized nanosilicon dioxide monomer, and initiating polymerization reaction on the functional polyamide and amine hybridized nanosilicon dioxide monomer, acrylamide, acrylic acid and a heat-resistant and salt-tolerant monomer by using a redox initiator or azobis(isobutylamidine) initiator. The hyperbranched polymer has a network structure with a polyamide and amine hybridized nanosilicon dioxide unit as a center, has excellent shear resistance, strong thickening property, heat resistance and salt tolerance, and is wide in adaptability and capable of being used as an oil displacement agent for increasing the recovery rate of raw oil in an oil field environment with a high mineralization degree and a wide temperature range; the preparation method of the polyamide and amine hybridized nanosilicon dioxide hyperbranched polymer is reliable in principle, simple and convenient to operate and wide in application prospect.

The invention relates to carbon dots with high fluorescent quantum yield, and an application thereof in fluorescent color development, and belongs to the application field of fluorescent carbon nanomaterials. Specifically, the invention relates to the carbon dots with the high fluorescent quantum yield which are synthesized by using citric acid and ethene diamine as raw materials as a fluorescent ink for writing or fluorescent printing, and further broadens the application thereof in fluorescent electrospining, fluorescent micro arrays and fluorescent composites. The carbon dots with the high fluorescent quantum yield are obtained by blending 1-100 mmol of citric acid and 1-100 mmol of ethene diamine in 5-100 mL of deionized water and transferring the mixture into a reaction kettle; carrying out a hydrothermal reaction for 2-10 hours at a temperature of 100-500 DEG C; cooling the reaction kettle to a room temperature after the reaction is finished to obtain a water solution of the carbon dots with the high fluorescent quantum yield; pouring the water solution of the carbon dots in a dialysis bag with a molecular weight of 3,500; dialyzing for 48-60 h; spin drying a dialysis outer solution and vacuum drying.

The present invention describes the use of porous metal oxides for the preparative purification of antibodies and biomolecules within a range of particle physical characteristics. Typically, particles from 15 to 100 microns in average diameter with pores sizes ranging from 400 to 600 angstroms and surface areas from 10 to 50 square meters per gram, and pore volumes from 0.1 to 0.4 mL/gram can be used for purification processes. The metal oxide particles that fall within this range of physical properties show enhanced utility and greater chromatographic capacity for antibodies than materials oxide particles falling outside of this range. Metal oxides such as zirconia, titania and alumina can all be modified with a multi-Lewis base moiety such as an organophosphate ethylenediamine-N,N-tetra(methylenephosphonic) acid (EDTPA), to produce a bio-compatible purification media for, biomolecules.

The invention discloses a super-hydrophobic reduced graphene oxide/sponge composite material and a preparation method thereof. The method includes: employing a microwave-ultrasonic wave method and using ethylenediamine as the reducing agent to reduce graphene oxide into reduced graphene oxide, and under the action of hole and other sound waves, dispersing and attaching the reduced graphene oxide to a commodity sponge, thus obtaining the super-hydrophobic reduced graphene oxide/sponge composite material. The method provided by the invention has the characteristics of simple operation, low cost, short reaction time, high efficiency and low energy consumption, and is beneficial to industrial mass production. The reduced graphene oxide/sponge composite material prepared by the method provided by the invention has excellent hydrophobic and oil absorption properties, large adsorption capacity and good stability, and can be used as a selective adsorbent for oily wastewater treatment.

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 polishing composition which achieves surfaces with high planarity and the reduction of corrosions in the wiring metal surface at the same time is provided.

Such compositions include

• • (A) an oxidizing agent;
  • (B) at least one acid selected from an amino acid, a carboxylic acid of no more than 8 carbon atoms, and an inorganic acid;
  • (C) a sulfonic acid having a concentration of 0.01% by mass or more and having an alkyl group of 8 or more carbon atoms;
  • (D) a fatty acid having a concentration of 0.001% by mass or more and having an alkyl group of 8 or more carbon atoms; and
  • (E) at least one compound selected from a pyridine carbonyl compound, a nonionic water-soluble polymer, 2-pyrrolidone, N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, gramine, adenine, N,N′-diisopropylethylenediamine, N,N′-bis(2-hydroxyethyl)ethylenediamine, N,N′-dibenzylethylenediamine, and N,N′-diphenylethylenediamine.

The invention relates to a preparation method of waterborne polyurethane capable of selfreparing. The preparation method includes the steps that hydrophilic chain extender is added to dihydric alcohol, heating for dehydration is conducted under a vacuum condition, the mixture is cooled to 70-85 DEG C, diisocyanate is added, stirring is conducted for a reaction, then the temperature is cooled to 50-55 DEG C, butanone is added, then a catalyst and the chain extender containing disulfide bonds are added, a reaction is conducted for 0.5-3 hours, then the temperature is cooled to 30-35 DEG C, neutralizer is added, then the mixture is cooled to 20-25 DEG C, distilled water is added, the mixture is stirred till emulsion and dispersion are achieved, ethidene diamine is added, chain extension is conducted for 0.5-1 hour, the butanone is removed, vacuum defomaing is conducted, and waterborne polyurethane capable of being self-repaired is obtained. The waterborne polyurethane prepared through the method can be self-repaired under the heating condition, the required condition is mild, the repairing effect is good, emulsion dispersion stability is good, operation is simple, and environmental friendliness is good.

A process for preparing a naphtha reforming catalyst has been developed. The process involves the use of a chelating ligand such as ethylenediaminetetraacetic acid (EDTA). The aqueous solution of the chelating ligand and a tin compound is used to impregnate a support, e.g., alumina extrudates. A platinum-group metal is also an essential component of the catalyst. Rhenium may also be a component. A reforming process using the catalyst has enhanced yield, activity, and stability for conversion of naphtha into valuable gasoline and aromatic products.