1539 results about "Ethylenediamines" patented technology

The invention discloses a CO2 trapping absorbent which comprises 20%-50% of proton type ionic liquid, 20%-50% of a phase conversion driving agent and 20%-40% of water, and the phase inversion driving agent is one or a mixture of more of N, N-dimethyl formamide, N-methyl pyrrolidone, pentamethyldiethylenetriamine, tetramethylethylenediamine, tetramethylethylenediamine, tetramethylenediamine, tetramethylethylenediamine and dimethyl piperazine, and the phase inversion driving agent is one or a mixture of more of N, N-dimethyl formamide, N-methyl pyrrolidone, pentamethyldiethylenetriamine, tetramethylethylenediamine, tetramethylethylenediamine and dimethyl piperazine. The absorbent disclosed by the invention has the outstanding advantages of low viscosity, high absorption rate, high regeneration efficiency, high circulation capacity and low regeneration energy consumption, and has a good application prospect.

The invention discloses an absorbable suture line for surgical suture and a preparation method thereof, and relates to the technical field of medical materials. The absorbable suture line for surgical suture is prepared from the following raw materials in parts by weight: 50 to 65 parts of polylactic acid, 15 to 20 parts of polyglycolic acid, 3 to 5 parts of sodium carboxymethyl cellulose, 3 to 8 parts of a toughening agent, 3 to 6 parts of an antibacterial agent, 0.3 to 0.8 part of a lubricating agent, 1 to 2 parts of sodium hyaluronate and 5 to 10 parts of polyvinyl alcohol. The toughening agent is obtained by reacting hydroxyethyl acrylate with ethylenediamine to generate a four-arm compound and then reacting with 6-caprolactone and DL-lactide. The absorbable suture line for surgical suture prepared by the invention has excellent tensile property and antibacterial property, and can meet the application requirements of clinical medical treatment.

The invention discloses an organic amine composite absorbent for carbon capture and application thereof, and belongs to the technical field of carbon dioxide capture, the organic amine composite absorbent for carbon capture is in a solution state and comprises the following components: a main agent, an auxiliary agent, an accelerant A, an accelerant B and water; wherein the mass ratio of the main agent to the auxiliary agent is 2: (1-2); the mass ratio of the auxiliary agent to the accelerant A is 2: (1-2); the mass ratio of the accelerant A to the accelerant B is 2: (1-2); the total mass concentration of the main agent, the auxiliary agent, the accelerant A and the accelerant B in the organic amine composite absorbent for carbon capture is 30-40 wt%; the main agent is selected from N-methyldiethanolamine or N, N-diethyl ethanolamine, the auxiliary agent is selected from piperazine or hydroxyethyl ethylenediamine, the accelerant A is selected from triethylene glycol monomethyl ether and / or ethylene glycol monomethyl ether, and the accelerant B is selected from ethyl butyl ether and / or isobutyl ether. The organic amine composite absorbent for carbon capture has a wide application prospect in removal of carbon dioxide in flue gas.

The invention discloses a preparation method of an In2O3-Cu-Cu2O ternary heterojunction catalyst and a preparation method of the In2O3-Cu-Cu2O ternary heterojunction catalyst. The method comprises the following steps: at room temperature and normal pressure, firstly, dissolving indium chloride tetrahydrate in a mixed solvent of ethylenediamine-ethylene glycol (the volume ratio is 1: 20-1: 30) and dihydric alcohol amine to obtain a homogeneous solution; then transferring the solution to a hydrothermal kettle, adding deionized water and Cu2O powder with different volumes, and carrying out hydrothermal crystallization at 160-200 DEG C for 10-14 hours; and centrifuging the obtained precipitate, alternately washing with water and alcohol for 2-3 times, carrying out vacuum drying at 60 DEG C for 5-7 hours, heating to 600 + / -10 DEG C at a speed of 3-5 DEG C / min in an N2 atmosphere, calcining for 3 hours, and cooling along with a furnace to obtain a target product. By adjusting the adding amount of the deionized water, the mass proportion of the three phases of In2O3, Cu and Cu2O can be continuously adjusted and controlled, and controllable preparation from'rich copper 'to'rich cuprous oxide' and'stable ternary 'is achieved.

The invention discloses a glue solution for a copper-clad plate and a preparation method of the glue solution, and relates to the technical field of copper-clad plates. According to the prepared glue solution for the copper-clad plate, the composite epoxy resin, the curing agent, the accelerant, the solvent, the flexibilizer and the inorganic filler, the composite epoxy resin comprises bisphenol A epoxy resin, epoxy phenyl polysiloxane, itaconic acid polyaryletherketone and hydroxyl-terminated fluorine-containing vinyl polysiloxane, so that the interface bonding force with the copper plate is enhanced; the dielectric constant and the dielectric loss are effectively reduced, the peel strength and the toughness of the material are also remarkably improved, and the toughening agent is modified polyether sulfone microspheres; the modified polyethersulfone microspheres are prepared by coating polyethersulfone microspheres with hexamethylenediamine tetrapropionamide diamine, the hexamethylenediamine tetrapropionamide diamine is prepared by carrying out acylation condensation reaction on hexamethylenediamine tetramethyl propionate and ethylenediamine, and the polyethersulfone microspheres are prepared by carrying out electrostatic spinning on a spinning solution of polyethersulfone and vinylpyridine, so that the peel strength of the glue solution is remarkably improved.

The invention discloses photocuring conductive hydrogel as well as a preparation method and application thereof. According to the invention, methacryloylethyl sulfobetaine (SBMA), acrylic acid (AA) and hydroxyethyl methylacrylate (HEMA) are used as comonomers, deionized water is used as a solvent, N, N '-methylenebisacrylamide (MBAA) is used as a cross-linking agent, ammonium persulfate (APS) is used as an initiator, tetramethylethylenediamine (TEMED) is used as an accelerator, and 2-hydroxy-4'-(2-hydroxyethoxy)-2-methyl propiophenone (Irgacure2959) is used as a photoinitiator; the conductivity is improved by adding an ionic compound potassium chloride (KCl), and the photocuring conductive hydrogel is prepared in a free radical polymerization manner by adopting an LED-UV curing box. The conductive hydrogel disclosed by the invention has the characteristics of good adhesion property, conductivity, mechanical property and the like, and has wide application in the fields of wearable strain sensors and other flexible electronics.

The invention provides a modified porous chitosan gel bead, a preparation method thereof and application of the modified porous chitosan gel bead in cobalt-nickel separation, and belongs to the technical field of chitosan preparation. The preparation method comprises the following steps: firstly, modifying chitosan by using polyethylene glycol and glutaraldehyde to obtain a porous chitosan gel bead with a cross-linked structure, and then grafting by using epichlorohydrin, ethylenediamine and 2-chloromethylpyridine hydrochloride to obtain the modified porous chitosan gel bead containing an aminomethylpyridine functional group. The modified porous chitosan gel bead has excellent selective adsorption on nickel ions in a cobalt-nickel solution with the pH value range of 2-5, and nickel-cobalt separation can be achieved. In addition, the modified porous chitosan gel bead also has a good nickel-cobalt separation effect in a salt-containing system. The preparation method of the modified porous chitosan gel bead provided by the invention is simple in process, and the raw material chitosan is wide in source, non-toxic and environment-friendly.

The invention belongs to the technical field of preparation of blocking removers, and particularly relates to a composite chelating blocking remover for an oil field and a preparation method of the composite chelating blocking remover. The composite chelating blocking remover for the oil field is prepared from the following raw materials in percentage by mass: 7 to 9 percent of 1-butyl-3-methylimidazole dodecyl sulfonate, 5 to 7 percent of erucamide propyl hydroxypropyl sulfobetaine, 3 to 4 percent of di-(2-ethylhexyl) sodium sulfosuccinate, 4 to 5 percent of ethylenediamine di-o-hydroxyphenylacetic acid, 5 to 7 percent of N, N '-di (2-hydroxybenzyl) ethylenediamine-N, N'-bis (2-hydroxybenzyl)-N, N '-bis (2-ethylhexyl)-N, N'-bis (2-hydroxybenzyl)-N, N '-bis (2-hydroxybenzyl)-N, N'-bis (2-hydroxyphenyl)-N, N '-bis (2-hydroxyphenyl)-N, N'-bis (2-hydroxyphenyl)-N The cleaning agent is prepared from the following components in percentage by weight: 3 to 4 percent of N, N '-diacetic acid, 2 to 3 percent of O-(3-(benzyloxy) propyl) hydroxylamine, 1 to 2 percent of heptadecenyl hydroxyethyl imidazoline quaternary ammonium salt, 1 to 1.5 percent of dimethyl diallyl ammonium chloride homopolymer and the balance of water. The composite chelating blocking remover for the oil field has excellent scale dissolution rate and paraffin inhibition rate when being applied to complex scale blocking removal of the oil field.

The invention discloses an implantable absorbable PLA composite material and a preparation method thereof, and relates to the technical field of medical materials. The implantable absorbable PLA composite material is prepared from the following raw materials in parts by weight: 60 to 70 parts of PLA, 5 to 10 parts of poly (lactic-co-glycolic acid), 8 to 12 parts of polycaprolactone, 5 to 8 parts of modified hydroxyapatite, 2 to 3 parts of a toughening agent and 0.2 to 0.6 part of an antioxidant, the toughening agent is prepared by the following steps: reacting hydroxyethyl methylacrylate with ethylenediamine to prepare a four-arm compound, reacting the four-arm compound with 1-chloro-4-isocyanatobutane to prepare an isocyanate compound, and finally reacting the isocyanate compound with polyethylene glycol. The implantable absorbable PLA composite material prepared by the invention has excellent tensile property and impact resistance, and can meet the application requirements of clinical medical treatment.

The invention provides an all-solid waste geopolymer grouting material and a preparation method thereof, and relates to the technical field of solid waste resource utilization and geopolymer grouting material preparation. The all-solid waste geopolymer grouting material comprises the following raw materials in parts by weight: 100-200 parts of an all-solid waste mixture, 40-50 parts of an alkaline activator, 0.1-0.5 part of an early strength agent, 0.5-1 part of a water reducing agent, 3-7 parts of a modifier and 70-90 parts of water, the all-solid waste material comprises slag powder, steel slag powder, phosphogypsum and fly ash; the modifying agent is prepared from aluminum dihydrogen phosphate, vinyl triacetoxysilane and ethylenediamine terminated polyethyleneimine. The all-solid waste geopolymer grouting material provided by the invention has the characteristics of good working performance, high early strength, micro-expansibility and the like.

The invention relates to the technical field of high-performance fibers, in particular to a high-performance fiber containing carbon nanotubes and a preparation method of the high-performance fiber. The preparation method comprises the following steps: adding ammonium polyphosphate, alkylphenol polyoxyethylene ether and tetraethyl orthosilicate to obtain a silicon-coated ammonium polyphosphate material; then adding a silicon-coated ammonium polyphosphate material and gamma-aminopropyltriethoxysilane, so as to obtain a modified silicon-coated ammonium polyphosphate material; and mixing the modified silicon-coated ammonium polyphosphate material, tannic acid and a buffer solution to obtain the double-layer coated ammonium polyphosphate material. The fiber is obtained by adding a carbon nanotube material, a double-layer coated ammonium polyphosphate material, polytrimethylene terephthalate, a compatilizer and polypropylene and carrying out melt spinning. And then the fibers are sequentially soaked in an ethylenediamine solution, a polyglutamic acid solution and a chitosan solution, and the high-performance fibers are obtained. The obtained high-performance fiber has good flame retardance and antibacterial property, so that the high-performance fiber has a wide application prospect in the technical field of high-performance fibers.

The invention relates to an ultraviolet deoxidizing and fresh-keeping packaging material and application thereof, and belongs to the technical field of packaging materials. According to the invention, trimethylolpropane triacrylate and ethylenediamine are used as raw materials, a hyperbranched polymer with terminal double bonds is constructed based on Michael addition, then a sulfydryl-containing hindered amine light stabilizer obtained by ester exchange of methyl thioglycolate and pentamethylpiperidinol is added, and the hindered amine light stabilizer and alkyl mercaptan are subjected to a sulfydryl-alkene click reaction together. The light stabilizer and plastic are subjected to melt blending and then subjected to curtain coating to form a film to serve as an outer layer, and one face of the outer layer is coated with coating liquid prepared from a dispersing agent, PET, an active substance capable of generating triplet excitons under irradiation of ultraviolet light, an antioxidant, an ultraviolet light absorber and a stabilizer. When the ultraviolet deoxidization fresh-keeping packaging material is applied to packaging of articles, deoxidization can be achieved through irradiation of ultraviolet light, and the degradation effect of the ultraviolet light on the outer layer is very little.

The invention discloses a long-life phosphorescent sulfur quantum dot, a multicolor long-life phosphorescent sulfur quantum dot composition and a preparation method and application thereof, and belongs to the technical field of phosphorescent materials and information encryption. The preparation method comprises the following steps: carrying out solvothermal reaction on a sulfur source and ethylenediamine to obtain sulfur quantum dots, and adding a sulfur quantum dot aqueous solution into a boric acid matrix to react to prepare long-life phosphorescent sulfur quantum dots (SQDs-MA); the long-life phosphorescent sulfur quantum dots and a rhodamine B aqueous solution are blended and dried to prepare the multicolor long-life phosphorescent sulfur quantum dot composition (RhB / SQDs-MA). When excited by ultraviolet light, the SQDs-MA shows a wide absorption range of 200 to 700 nm. When excitation is carried out at 362 nm, the SQDs-MA shows a blue fluorescence emission peak at 436 nm. The SQDs-MA powder emits bright green phosphorescence after the irradiation of an ultraviolet lamp is turned off, and under the optimal excitation of 373 nm, the maximum phosphorescence emission value is displayed at 526 nm. Under the irradiation of ultraviolet light, the RhB / SQDs-MA can emit yellow, orange and red phosphorescence at the wavelength of 584 nm, 600 nm and 620 nm.

The invention belongs to the technical field of preparation of hot melt adhesives, and particularly relates to a high-strength quick-curing bio-based hot melt adhesive and a preparation method thereof. The preparation method comprises the following steps: preparing a dimer acid polymer from dimer acid, sebacic acid, polyether amine, ethylenediamine, an antioxidant and a catalyst, and mixing the dimer acid polymer with a beta nucleating agent toughened polypropylene / SiO2 nano-composite and an organic borosiloxane polymer to obtain the high-strength quick-curing bio-based hot melt adhesive. The prepared hot melt adhesive has good mechanical property, viscosity and self-healing property.

The invention provides a rapid visual D-limonene detection method and application thereof, and belongs to the technical field of analytical chemistry, the method comprises the following steps: uniformly mixing ethanol and water to form a solvent system, sequentially adding template agents Pluronic P123 and Pluronic F127, phloroglucinol, 1, 3, 5-trimethylbenzene and ethylenediamine, and uniformly stirring at room temperature; after the reaction is completed, washing, centrifuging, drying and calcining an obtained sample to obtain DNCzyme; the method comprises the following steps: adding TMB, H2O2 and DNCzyme into an acetic acid-sodium acetate buffer solution HAc-NaAc, finally adding D-limonene, incubating, and carrying out visual detection on the solution. The method for detecting the D-limonene through colorimetric sensing is rapid, simple, convenient, low in cost, high in sensitivity and good in selectivity, and visual detection is achieved by combining a smart phone.

The invention belongs to the technical field of photovoltaic coatings, and discloses a photovoltaic coating as well as a preparation method and application thereof. The photovoltaic coating is prepared from the following raw materials: a solvent, an ultraviolet light absorber, a wetting agent, an antistatic agent, modified hydrophilic silicon dioxide, nano magnesium fluoride and nano tin dioxide, the modified hydrophilic silicon dioxide is hydrophilic silicon dioxide modified by ethylenediamine and glacial acetic acid. A coating formed by the photovoltaic coating is high in adhesive force and resistant to aging, and the light transmittance, the self-cleaning property and the antistatic property of photovoltaic glass can be obviously improved.

The invention relates to the technical field of battery current collectors, and discloses a high-conductivity stainless steel foil for a positive current collector and a preparation method of the high-conductivity stainless steel foil. Comprising the following operation steps that 1, stainless steel foil is subjected to acid pickling and then dried, the stainless steel foil is soaked in an ethylenediamine tetramethylenephosphonic acid ethanol solution to be stirred for 2-3 h in the nitrogen atmosphere, the stainless steel foil is taken out to be cleaned and cured for 3-4 h at the temperature of 120-125 DEG C, after the stainless steel foil is cooled to the room temperature, washing and nitrogen drying are conducted, and prefabricated stainless steel foil is obtained; and 2, the prefabricated stainless steel foil is soaked in the anti-oxidation conductive copper composite sol for 25-40 s, taken out, dried, coated with an aluminum grid, ground, soaked in the graphene / carbon nanotube composite sol for 20-30 s, taken out, dried for 4-6 min at the temperature of 100-120 DEG C, ground and dried, and the high-conductivity stainless steel foil is obtained.

The invention discloses a method for enhancing Candida albicans biofilm resistance of azole drugs by using a zinc ion chelating agent, through the combined action of the zinc ion chelating agent N, N, N ', N'-tetra (2-picolyl) ethylenediamine (TPEN) and fluconazole, the activity of the Candida albicans biofilm can be reduced, and the Candida albicans biofilm can be enhanced. The early-stage adhesion process, the medium-stage yeast-to-hypha conversion process and the late-stage maturation process formed by the candida albicans biological membrane are inhibited, the structure of the candida albicans biological membrane is destroyed, then the high drug resistance of the candida albicans biological membrane to fluconazole is reversed, and the pathogenicity of the fluconazole is reduced; the problems of high drug resistance and sustained infection caused by the formation of a candida albicans biofilm are hopefully solved, and a direction is provided for the treatment of clinical fungal infection and the research and development of drugs.

The invention provides a gel composite adsorbent with a foaming structure as well as a preparation method and application thereof, and the preparation method comprises the following steps: S1, dissolving acrylamide powder in deionized water, and stirring to obtain a solution A; s2, dissolving sodium alginate in the solution A for thickening to obtain a solution B; s3, transferring the solution B into an ice-water bath; s4, adding N, N-methylene bisacrylamide into the solution B, stirring until the N, N-methylene bisacrylamide is completely dissolved, then adding N, N, N ', N'-tetramethylethylenediamine, and stirring until the N, N, N ', N'-tetramethylethylenediamine is uniform to obtain a solution C; s5, adding ammonium persulfate into the solution C, and stirring until the ammonium persulfate is completely dissolved to obtain a solution D; s6, the solution D is poured into a mold and then vacuumized to form gel, and a hydrogel sample is obtained after gel forming; s7, drying the hydrogel sample, and then soaking the dried hydrogel sample in a salt solution to obtain a soaked gel material; and S8, drying the soaked gel material to obtain the finished product composite adsorbent.

The invention discloses a carbon-based catalyst and a preparation method and application thereof to isomerization of glucose into fructose, the catalyst comprises an active component loaded on a carbon-based catalyst carrier and a chelating agent complexed with the active component, metal salts in the active component are Mg and K, the chelating agent is one or more of citric acid, triacetic acid, triethylamine ethylenediamine and potassium sodium tartrate. The chelating agent adjusts alkali active sites of a reaction system through acidic functional groups of the chelating agent, maintains an acid-base environment required by the reaction, and promotes an isomerization reaction from glucose to fructose. Meanwhile, the chelating agent and the metal ions form a stable complex to prevent metal salt from inactivation, and the metal ions are ensured to be uniformly distributed on the surface of the carrier and prevented from being agglomerated through the dispersity of the chelating agent, so that the activity and stability of the catalyst are improved. By controlling the dosage of the chelating agent and coordination of metal ions, the selectivity of the glucose isomerization reaction and the fructose yield are effectively improved, side reactions are inhibited, and the overall efficiency of the reaction is remarkably improved.

The invention provides an efficient and environment-friendly reverse osmosis membrane scale inhibition cleaning agent based on a composite formula, and relates to the field of reverse osmosis membrane cleaning. Comprising effective components and water, and the effective components comprise the following raw materials in percentage by mass: 10-15% of a surfactant, 10-15% of a sterilizing agent, 30-40% of a composite chelating agent, 10-20% of slow-release organic acid, 5-10% of compound enzyme, 5-10% of an oxidizing agent and 1-5% of a defoaming agent; the composite chelating agent is a compound which takes attapulgite and montmorillonite as carriers and is loaded with hydroxyethyl ethylenediamine triacetic acid trisodium salt; the slow-release organic acid is citric acid modified by carboxymethyl chitosan. The cleaning agent provided by the invention contains the composite chelating agent, the slow-release organic acid, the compound enzyme, the surfactant, the sterilizing agent and the like in effective components, is prepared into the cleaning agent with water, has the effect of efficiently cleaning the reverse osmosis membrane, and is high in cleaning efficiency and small in damage to the reverse osmosis membrane.

The invention discloses a method for preparing ethylenediamine and piperazine from ethylene glycol, which comprises the following steps: in a system containing ethylene glycol, ammonia gas, hydrogen, a solvent and a catalyst, carrying out dehydrogenation, amination and hydrogenation on ethylene glycol and ammonia gas under the action of the catalyst to generate ethanolamine; the ethanolamine is further aminated to generate ethidene diamine; and further reacting ethylene glycol, ethanolamine and ethylenediamine to generate piperazine. According to the present invention, the solubility of ethanolamine and ethylenediamine is increased by introducing the solvent with the high polarity into the reaction system, such that the high ethylene glycol conversion rate is achieved under the mild reaction conditions (180-220 DEG C, 4-5 MPa), and the selectivity of ethylenediamine and piperazine is significantly improved. Wherein the selectivity of ethylene glycol can reach 74.1%, the sum of the selectivity of ethanediamine and piperazine can reach 85.5%, and the selectivity of piperazine can reach 73.3%.

The present invention discloses a platinum electroplating solution, a preparation method thereof and an application in semiconductors, which comprises the following raw materials: 0.5-10 g / L of platinum salt PEP, 15-35 g / L of ethylenediamine sulfate, 5.0-29 g / L of malonic acid, 5.0-40 g / L of ammonium acetate, the balance being ultrapure water and ammonia water; the pH value of the platinum electroplating solution is adjusted to 7.0 with ammonia water; the method for preparing the coating comprises the following steps: S1, degreasing and pickling the semiconductor device to be processed; S2, selecting corresponding electroplating conditions and configuring a corresponding anode and its anode mask; S3, performing electroplating; S4, automatically adding the platinum salt PEP solution in a linked manner; S5, adjusting the pH value of the platinum electroplating solution; S6, stopping electroplating after reaching the target coating thickness or the preset electroplating time. The platinum metal film formed by the present invention has excellent morphology, uniform distribution, high wear resistance and excellent compactness.

The invention discloses a preparation method and application of a wear-resistant TPE (thermoplastic elastomer) material for data lines, and the preparation method comprises the following steps: carrying out reaction on polytetrahydrofuran ether glycol and isophorone diisocyanate to form a polyurethane prepolymer, adding a reinforcing monomer and a modified filler, carrying out chain extension reaction, and finally adding ethylenediamine to prepare the wear-resistant TPE material. The TPE material is of a hyperbranched structure, the mechanical performance of the material can be improved, cross-linking points of the TPE material are increased by adding the modified filler, TPE material molecules form a stable grid shape, the wear resistance of the TPE material is further improved, a zinc organic framework is connected between the modified filler and a polyurethane prepolymer molecular chain, and the modified filler contains a six-membered ring structure, so that the wear resistance of the TPE material is improved. According to the present invention, the modified filler is added to the TPE material, such that the TPE material can well adapt to the surface contact when the TPE material is worn so as to reduce the wear, and the dynamic cross-linking of the modified filler and the TPE material molecules does not cause the substantial reduction of the toughness due to the increase of the cross-linking point so as to improve the bending resistance effect of the TPE material.

The invention discloses a synthesis method of an aryl bidentate phosphine compound, which comprises the following steps of: (1) reacting benzene or alkylbenzene with benzyl chloride or 4-alkyl benzyl chloride at 0-100 DEG C for 0.5-5 hours in the absence of oxygen and under the condition of a lewis acid catalyst to prepare a first intermediate; (2) dropwise adding an alkyl lithium reagent into tetramethylethylenediamine at the temperature of-30 to 40 DEG C under the conditions of no water, no oxygen and a solvent, stirring for 1 to 3 hours, dropwise adding the first intermediate into the mixed solution at normal temperature, and reacting for 4 to 20 hours at the temperature of-20 to 40 DEG C to prepare a second intermediate; and (3) under anhydrous and anaerobic conditions, adding diphenyl phosphine chloride into the second intermediate obtained in the step (2), and reacting at-20 to 80 DEG C for 5-60 hours to obtain the aryl bidentate phosphine compound. The synthesis method disclosed by the invention is simple in process, mild in condition and high in product yield, and has a relatively good industrial prospect.

The invention discloses a preparation method of salt-resistant sodium carboxymethyl cellulose, and relates to the technical field of petroleum fracturing materials. The preparation method comprises the following steps: reacting stearic acid with ethylenediamine to obtain a monosubstituted intermediate, reacting the monosubstituted intermediate with cocoyl chloride to obtain an intermediate 1, reacting the intermediate 1 with epoxypropane to obtain an intermediate 2, and reacting the intermediate 2 with paratoluensulfonyl chloride to obtain a hydrophobic intermediate; reacting a sodium carboxymethyl cellulose solution with the hydrophobic intermediate to obtain modified sodium carboxymethyl cellulose, and sulfonating the modified sodium carboxymethyl cellulose with sulfamic acid to obtain crude salt-tolerant sodium carboxymethyl cellulose; and reacting the crude product salt-resistant sodium carboxymethyl cellulose with borax to obtain the salt-resistant sodium carboxymethyl cellulose. The salt-resistant sodium carboxymethyl cellulose prepared by adopting a step-by-step synthesis strategy has excellent salt resistance, temperature resistance, shearing resistance and dissolution rate, and is suitable for thickening and sand carrying of high-temperature and high-salt oil and gas field fracturing fluid.

The invention discloses an embedded catalyst as well as a preparation method and application thereof. The embedded catalyst comprises a carrier, a main active component Pt and an optional auxiliary active component M, wherein the main active component Pt and the optional auxiliary active component M are embedded into the carrier; wherein the carrier is a pure silicon molecular sieve; the auxiliary active component M is selected from one or more of Zn, Ga, Sn, In and K. According to the embedded catalyst disclosed by the invention, the Al-free pure silicon molecular sieve is used as the carrier, the silicon source is dissolved and the pure silicon molecular sieve is grown in situ through the structure guiding effect of the template agent, and the active metal component is embedded into the skeleton structure of the carrier, so that the metal substance is stabilized, and the sintering and migration of the metal substance are avoided. The catalyst prepared by the invention has high ethane catalytic dehydrogenation activity and stability, and realizes high ethylene selectivity (greater than or equal to 95%); meanwhile, ammonia-containing and fluorine-containing substances are not added in the preparation process; flammable and explosive ethylenediamine is not used; the catalyst raw materials are cheap, easily available and low in cost.

The invention relates to the technical field of resin for printing ink, and discloses alcohol-soluble polyamide resin for printing ink and a preparation method and application thereof.The alcohol-soluble polyamide resin is prepared from, by weight, 78-83 parts of vegetable oil dimer acid, 3-5 parts of ethidene diamine, 6-7 parts of hexamethylenediamine, 5-8 parts of methyl pentamethylene diamine, 3-5 parts of propionic acid and 2-3 parts of acrylic acid through condensation reaction, and a defoaming agent (10-15) ml / ton. The alcohol-soluble polyamide resin for ink provided by the invention is non-toxic, free of pungent smell, non-corrosive, non-combustible, non-explosive, excellent in adhesive force, excellent in gloss, particularly strong in freezing resistance and gel resistance, excellent in alcohol solubility, stability and solvent release property, and can be used for preparing gravure plastic film surface printing ink.

The invention discloses a high-bonding-strength conductive adhesive and a preparation method and application thereof.The preparation method comprises the following steps that S1, epoxy resin E51 is placed in a three-neck flask, acetone is added, stirring is conducted till the epoxy resin E51 is completely dissolved, and ethidene diamine is slowly dropwise added; s2, under the protection of nitrogen, heating to 70-80 DEG C, adding a catalyst triphenylphosphine, carrying out a constant-temperature reaction, after the reaction is completed, cooling to 35-45 DEG C, adding deionized water, and stirring; s3, acetone and unreacted ethylenediamine are removed, then deionized water is used for washing, an obtained product is placed in a vacuum drying oven to be dried, and amino modified epoxy resin of faint yellow viscous liquid is obtained; s4, mixing the amino modified epoxy resin with an anhydride curing agent, a conductive filler, a diluent and a coupling agent; and S5, fully stirring the mixture, carrying out vacuum defoaming, and uniformly stirring to obtain the conductive adhesive. According to the invention, the shearing strength of the chip and the copper bracket can be improved to more than 30MPa.

The invention relates to a method for generating a perovskite in-situ film through assistance of an interface protonation reaction, and the method comprises the following steps: S1, spin coating: carrying out the spin coating of a perovskite precursor solution on an acidic substrate, and forming a complex intermediate phase; the perovskite precursor solution comprises a tin halide, a monovalent cation halide, thiocyanate and an ethylenediamine derivative; s2, annealing: heating and annealing the intermediate phase of the complex on a heating stage, and inducing conversion of the intermediate phase of the complex to the tin-based perovskite thin film through a protonation reaction between the acidic substrate and the ethylenediamine derivative; the chemical structure of the tin-based perovskite is ASnX3. According to the method, the protonation reaction of the acidic substrate and the perovskite interface is utilized to assist in generating high-quality perovskite, the morphology of the thin film is effectively improved, and a high-brightness PeLED device is further prepared.