2412 results about "Ethylenediamines" patented technology

The invention discloses high-quantum-yield fluorescence carbon quantum dots and a preparation method thereof. The method comprises the following steps: by using chitosan as a carbon source, adding glacial acetic acid and ethylenediamine, and sufficiently stirring to obtain a paste; reacting in a microwave oven to finally obtain a black solid; taking out, naturally cooling, adding a certain amount of secondary water, dissolving by stirring to obtain a brown solution, removing the insoluble substance to obtain a brown solution, dialyzing to remove impurities to obtain a fluorescence carbon quantum dot water solution, and carrying out freeze-drying to obtain the fluorescence carbon quantum dots. The method has the advantages of simple technique, wide raw material sources, low price, low requirements for preparation conditions and higher quantum yield of the obtained carbon quantum dots. The obtained fluorescence carbon quantum dots can be used for detecting Fe<3+> in a water body, and can also be used in living cell fluorescence imaging.

The invention relates to a method for preparing ethylenediamine modified chitosan composite magnetic microspheres and application thereof. The method specifically comprises the following steps of: mixing acidic aqueous solution of chitosan and a water-based magnetofluid first, then crosslinking by using glutaraldehyde, then adjusting the pH value to form a gelatinous precipitate, then modifying by using ethylenediamine and epichlorohydrin, and washing and drying to obtain a final product. The product has good absorption effect on radionuclide aranium and metal ions such as heavy metal Pb, Cr and the like; the removal rate reaches over 95 percent when the initial concentration of various ions is within the range of 200mg/L; and the product has quick absorption rate and good regeneration performance. The ethylenediamine modified chitosan composite magnetic microspheres can be used for metal recovery and pollution remediation in mines, radioactive waste water, smelteries, electronics factories and waste water of electroplating factories.

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 invention discloses graphene aerogel and a preparation method thereof. The method comprises the following steps: (1) uniformly mixing graphene oxide dispersion liquid with an amine water-soluble compound to obtain graphene oxide mixed liquid, wherein the amine water-soluble compound is selected from one or more of diethylamine, ethidene diamine, propane diamine, butane diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, allylamine polymer and N,N'-bis(2-aminoethyl)-1,3-propane diamine; (2) irradiating the graphene oxide mixed liquid by high-energy rays under the anaerobic condition to obtain amino-modified graphene aerogel; (3) performing freeze-drying or supercritical CO2 drying to obtain the graphene aerogel. The graphene aerogel adopts a porous and macroporous structure, is relatively uniform in structure, and can be used for adsorbing an organic solvent; moreover, the preparation method is simple and environment-friendly.

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 discloses a phenyl bistriazole compound, and a preparation method and application thereof, and particularly relates to a 1-[4-(1H-1,2,4-triazole-1-yl)phenyl]-1H-1,2,4-triazole single crystal and a preparation method of 1-[4-(1H-1,2,4-triazole-1-yl)phenyl]-1H-1,2,4-triazole. The organic compound is prepared by heating ethylenediamine, 1H-1,2,4-triazole, potassium carbonate, 1,4-diiodobenzene and cuprous iodide through a one-pot method. The preparation method disclosed by the invention has the characteristics simple process operation, low production cost and less environmental pollution, and is suitable for large-scale industrial production. The 1-[4-(1H-1,2,4-triazole-1-yl)phenyl]-1H-1,2,4-triazole single crystal prepared by the invention can be used in the aspect of photoelectric materials, especially dye and luminescent agents.

The invention discloses an adsorbent used for efficiently separating formaldehyde from air and a preparation method thereof. An adsorbent carrier is active carbon, the surface of which is attached with one or more of -NH, -NH2 and -NH3. The precursor of -NH, -NH2 and -NH3 is one of salvolatile, ammonium bicarbonate, ammonium sulfate, ammonium nitrate, ammonium chloride, ethene diamine, hexamethylenediamine, aniline and urea. The adsorbent can absorb and separate formaldehyde in air when space velocity is 20000-80000h<-1> at room temperature. Especially when the formaldehyde and benzene seriesin the air coexist, the adsorbent not only can absorb and separate formaldehyde but also can absorb and separate the benzene series. Therefore, the adsorbent can be widely applied to the purifying treatment of air in hermetic and semi-hermetic limited spaces, such as building interiors, spacecrafts, submarines, undergrounds and the like.

The invention discloses acrylate grafted aqueous polyurethane emulsion and a preparation method thereof. The emulsion is characterized is prepared from polyether polyol, dimethylol propionic acid, isophorone diisocyanate, ethylenediamine, hydroxyethyl acrylate and the like. The preparation method comprises the following steps: carrying out prepolymerization on polyether polyol, dimethylol propionic acid and isophorone diisocyanate so as to introduce a hydrophilic monomer; adding ethylenediamine and hydroxyethyl acrylate to carry out chain extension so as to introduce a functional monomer; adding an acrylate mixed monomer so as to reduce system viscosity; adding triethylamine for neutralization; adding deionized water for emulsification and dispersion under the condition of high-speed shearing to obtain emulsion; then dropwise adding the acrylate mixed monomer and an initiator, raising the temperature and carrying out reaction; and cooling to obtain the PUA (polyurethane-acrylate) emulsion. The emulsion prepared by the method has small grain size and excellent performances such as mechanical performance, is narrowly distributed and can be widely applied to industry fields such as leather finish, coatings, adhesives and fabric coatings.

The invention relates to an ester type fire-resistant hydraulic fluid. The hydraulic fluid comprises the following raw materials by weight percent: 95-99% of base oil, 1.0-5.0% of diphenol propane, 0.005% of dimethylsilicone fluid or dimethylsilicone grease, 0.05% of tricresyl phosphate, 0.1% of benzotriazole, 100 parts per million (PPM) demulsifying agent T1001 or LZ5957 and 0.2-0.3% of triazole derivative, thiadiazole derivative, N-salicylidene ethylamine, N, N'-bis(salicylidene)ethylenediamine, N, N'-bis(salicylidene)propylene diamine or ethylenediamine tetraacetic acid. A preparation method of the ester type fire-resistant hydraulic fluid comprises the following steps of sufficiently and evenly stirring various materials at room temperature according to a formula, and then filtering. The ester type fire-resistant hydraulic fluid has the beneficial effects that the high temperature use performance of the product is greatly improved, the service life of a hydraulic system and the oil changing period of oils are prolonged, and the ester type fire-resistant hydraulic fluid has a good flame-retardant effect and is safe to use. The preparation method has the advantages that operation is convenient, technology and equipment are simple, energy consumption is low, cost is low, and the like.

The invention discloses a preparation method of a graphene/polyacrylic ester-silicon-containing hyperbranched waterborne polyurethane multi-element composite emulsion. The method comprises the following steps: preparing graphene oxide (GO) by an improved Hummers method, modifying the GO by ethanediamine, enabling reaction with butyl acrylate to introduce double bonds to obtain MGO (ethylenediamined graphene oxide), and performing solution polymerization on the MGO and an acrylic ester monomer in DMF to prepare an MGO/PA solution; and grafting a partial double-bond end-sealed hydroxyl silicone oil modified linear polyurethane prepolymer, which is prepared by in-situ polymerization, on the periphery of a polyhydroxyl hydrophilic hyperbranched polyurethane core by diisocyanate, an oligomer dihydric alcohol and a chain extender and by a hyperbranched polymer chain extending method, mixing with the MGO/PA, and performing polycondensation and crosslinkage to obtain aminated graphene oxide/polyacrylic ester-silicon-containing hyperbranched polyurethane quaternary composite emulsion.

The invention relates to the technical field of textile printing and dyeing and provides a low-temperature soaping agent. The low-temperature soaping agent can soap surface dyeing of a dyed object at a lower temperature (60 DEG C), is not easy to foam, can chelate metal ions, has stronger combined dyeing capability and effectively prevents from staining. Meanwhile, the invention further provides a method for preparing the low-temperature soaping agent and an application of the low-temperature soaping agent. The low-temperature soaping agent is prepared from the following components in percentage by weight: 50-75% of maleic-acrylic copolymer, 5-15% of a surfactant, 0.1-0.5% of a de-foaming agent, 1-5% of ethanediamine di-o-hydroxyphenyl sodium acetate and the balance of de-ionized water.

The invention relates to a preparation formula of a polishing solution for precision polishing of an LED sapphire substrate. The polishing solution comprises the following components in percentage by weight: 0.7-1.0% of organic base diethanol amine, 25-35% of silica solution with grain diameter of 50-70nm, 0.4-0.7% of dispersing agent ethanediamine, and 0.1-0.3% of activating agent nonylphenol polyoxyethylene ether. The removal rate of the polishing solution can be up to 28 nm/min; the surface roughness Ra is smaller than 0.5 nm, which can meet the main performance index requirements for sapphire substrate CMP (chemical mechanical polishing). The polishing solution has the advantages of high removal rate, low surface roughness and cost, non-pollution to the environment and non-corrosion to equipment.

The invention relates to a palladium coordination polymer molecule aggregate catalysis material as well as a preparation method and an application thereof. The catalysis material is a coordination polymer molecule aggregate catalysis material formed by self-assembling on the surface of a solid substrate, the precursor of the catalysis material comprises palladium coordination ion as well as pyridine containing multidentate ligand or high molecular ligand, wherein the palladium coordination ion is selected from one of tetrachloro combined palladium acid radical, dichloro-2, 2'-dipyridine palladous, and dichloroacetamide palladous, and the pyridine containing multidentate ligand or high molecular ligand is selected from one of 4, 4'-combined pyridine, 2, 4, 6- collidine triazine, metal or hollow tetra pyridyl porphyrin, trans-1, 2- collidine ethylene, combined dipyridylzinc thiocyanate and polyethylene pyridine. LB film preparation technology or layered assembly method is adopted for organism selective ethylenic bond organic hydrogenation reaction, thus having high catalysis efficiency, easy realization in separation of catalyst and reactant and product, convenient operation and low cost.

The invention relates to a method for preparing cyclic carbonate by reacting normal pressure carbon dioxide with epoxide. Propylene carbonate or ethylene carbonate is prepared by reaction under normal pressure carbon dioxide by taking epoxypropane or ethylene oxide as a substrate, corresponding propylene carbonate or ethylene carbonate as a solvent and Salen-Zn and tetraethyl ammonium bromide as a dual component catalyst, wherein the Salen-Zn is bissalicylaldehyde ethylenediamine-Zn, salicyladehyde cyclohexanediamine-Zn or bis-salicylaldehyde o-phenylenediamine-Zn. The method provided by the invention has the advantages that the catalyst is convenient to prepare, low in cost and less in use level; by using the product as the solvent, posttreatment is convenient; the method is low in reaction pressure, great in rate, safe to operate and suitable for scaled industrial production.

The invention belongs to the technical field of nanomaterials and particularly relates to a doped carbon dot and graphene compound as well as a preparation method and an application thereof. The preparation method comprises the steps as follows: lipoic acid, ethylenediamine, phytic acid and the like are used as mixed element precursors to be dissolved in deionized water and uniformly mixed, and doped carbon dots are obtained through a hydrothermal reaction in a reaction kettle; the carbon dots are added to a graphene oxide aqueous solution to be subjected to a hydrothermal reaction, then washing and drying are performed, and the doped carbon dot and graphene compound is obtained. The electro-catalysis effect best for oxygen reduction can be obtained by adjusting the type of mixed elements in the carbon dots and the proportion of the carbon dots to graphene. The preparation method is simple and easy to implement and low in cost; the chemical and physical properties of the obtained material are stable, a representative nitrogen and sulfur double-doped carbon dot-graphene composite can realize the four-electron transfer process for oxygen reduction, the reduction overpotential is obviously smaller than that of single-doped samples and other doped samples, and the material can be applied to electro-catalysis of oxygen reduction reactions on cathodes of fuel cells.

The invention discloses a nitrogen doped reduced graphene oxide aerogel (NGA) wave-absorbing material and a preparation method thereof. According to the preparation method, nitrogen doped reduced graphene oxide hydrogel is formed through in-situ self-assembly of a one-step hydrothermal method by taking graphene oxide (GO) aqueous dispersion as a template and ethylenediamine (EDA) as a nitrogen doping agent and reducing agent, and the nitrogen doped NGA wave-absorbing material through dialysis and lyophilizing. The preparation method is environment-friendly, and has the advantages of no toxic or side product generation, simple preparation process, mild reaction condition and low cost. The aerogel wave-absorbing material has strong electromagnetic wave absorbing performance, wide absorptionfrequency band, low density and low packing ration, electromagnetic waves at different wavebands can be effectively absorbed by adjusting the nitrogen doping amount and thickness of a wave-absorbing coating, so that the NGA wave-absorbing material has an important application value in the field of electromagnetic absorption and electromagnetic shielding.