4215 results about "Ethylene glycol" patented technology

The invention relates to the field of packaging materials, and discloses low-temperature heat-sealing water-based coated paper and a preparation method and application thereof.The water-based coated paper comprises a base paper layer and a water-based coating, and the water-based coating comprises water-based ethylene-acrylic acid copolymer emulsion, modified nano-silica, a coalescing agent and water; a cardanol derivative is introduced into the water-based ethylene-acrylic acid copolymer emulsion as a functional component; the cardanol derivative is prepared by reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and then grafting with acryloyl chloride. The preparation method comprises the following steps: reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide; the modified nano silicon dioxide is prepared by mixing aminated nano silicon dioxide and chitosan and adding a cross-linking agent prepared by grafting phytic acid and ethylene glycol diglycidyl ether. The water-based coating paper prepared by the invention overcomes the defects that the existing BOPP film is not environment-friendly, and the conventional coating paper is high in heat sealing temperature and easy to stick; meanwhile, good mechanical properties, water resistance and flame retardance are achieved.

The invention belongs to the technical field of high polymer materials, and particularly relates to a high-strength papermaking forming net fiber. Comprising the following raw materials in parts by weight: 75-90 parts of polyethylene glycol terephthalate, 5-15 parts of polybutylene terephthalate, 3-10 parts of a modified fiber filler, 2-5 parts of modified graphene, 2-8 parts of silicon dioxide, 0.5-2 parts of a silane coupling agent KH-560, 1-3 parts of an anti-hydrolysis agent, 0.5-1.5 parts of an antioxidant and 0.3-1 part of a lubricant. Wherein the modified fiber filler is prepared by sequentially carrying out modification processes such as silane coupling agent, citric acid-glycerol esterification, iron bismuth oxide loading and the like on glass fibers; the modified graphene is prepared by introducing dopamine, cerium ions and glycidyl methacrylate for modification. The mechanical strength, the hydrolysis resistance and the wear resistance of the fiber are remarkably improved through the synergistic effect of all the components and the melt spinning-multi-stage stretching process, and the fiber is particularly suitable for a forming net of a high-speed paper machine.

The invention relates to the technical field of pavement materials, in particular to a solid waste-based cementing material stable coal-based solid waste road base material and a preparation method thereof. According to the material, secondary modified regenerated coarse and fine aggregate is used as a framework, coal gangue powder and granulated blast furnace slag micro powder are matched, and two-step engineering of dopamine / double-amino-terminated polyethylene glycol co-deposition grafting and high-modulus silicate pre-coating is adopted, so that the synergistic improvement of the surface wettability and the interface density of the aggregate is realized. The system is cooperated with low-modulus excitation liquid and polypropylene fibers, and the mixing uniformity of the material and the quality of an interface transition area are optimized through a thin-pulp stone-wrapping and densification segmentation process. The material gives consideration to high resilience modulus, rut resistance and durability, significantly reduces the problems of high water absorption, weak interface, early cracks and the like of the recycled aggregate, is adaptive to a traditional road construction window, and has good application prospects.

The invention relates to a sunken porous magnetic alloy ball wave-absorbing material and a preparation method and application thereof.The wave-absorbing material is prepared through the following steps that S1, citric acid, soluble ferric salt, soluble cobalt salt and soluble nickel salt are dissolved in a mixed solvent of ethylene glycol and water, and the mixture is fully stirred to form a uniform mixed solution; and S2, the mixed solution obtained in the step S1 is subjected to spray drying, obtained precursor powder is placed in the air atmosphere to be calcined to remove the carbon source, then the precursor powder is placed in the H2 / Ar atmosphere to be subjected to heating reduction, and the porous FeCoNi alloy balls with the surface pits are obtained and are the target product. The surface of the prepared alloy microsphere has an obvious concave structure, magnetic anisotropy and magnetic performance are enhanced, a small number of pores are generated in the reduction process, impedance matching of the material is optimized, and effective high-frequency electromagnetic absorption is achieved; and due to the synergistic effect of the recesses and the pores, the obtained alloy microspheres have obvious lightweight characteristic, and have good application prospects in the field of electromagnetic absorption.

The invention relates to the field of coatings, and discloses a biomass-based oil-resistant coating and a preparation method thereof, the coating comprises an additive solution, a paraffin solution and gallic acid; the paraffin solution is obtained by dissolving paraffin in absolute ethyl alcohol; a preparation method of the additive solution comprises the following steps: mixing chitosan powder and an acetic acid aqueous solution to prepare a chitosan solution, ultrasonically dispersing functionalized montmorillonite in deionized water to prepare a suspension, then uniformly mixing the chitosan solution and the suspension, adding modified phytic acid prepared by grafting phytic acid and ethylene glycol diglycidyl ether, and stirring to react; the functional montmorillonite is prepared by modifying modified montmorillonite with titanium dioxide and zinc oxide, then activating the modified montmorillonite with 3-aminopropyltriethoxysilane and succinic anhydride, and then carrying out a ring-opening reaction with glycidyl neodecanoate. The coating prepared by the invention has high water resistance, the Kit oil-proof grade is kept at grade 12, and the oil-proof performance of the coating is greatly improved. Meanwhile, the antibacterial performance, the tensile index and the ultraviolet aging resistance are relatively high.

The invention discloses a preparation method of a raspberry-derived exosome loaded with neroli essential oil. The preparation method comprises the following steps: preparing raspberry fruits into homogenate; centrifuging, collecting supernate, adjusting the pH value to 4.07.5, standing, and centrifuging again; taking supernate, adjusting the pH value to 7.2-7.4, adding polyethylene glycol, standing, centrifuging, collecting precipitate, and carrying out resuspension dispersion; performing microfiltration to obtain supernate, and combining electrophoresis dialysis and ultrafiltration concentration to obtain the high-purity raspberry exosome. And diluting the exosome, adding the diluted exosome into a dimethyl sulfoxide solution containing neroli essential oil, carrying out water bath stirring, carrying out ultrafiltration centrifugation, and taking a clear liquid to obtain the exosome loaded with the neroli essential oil. Efficient separation and purification of the raspberry exosome are achieved by applying an isoelectric precipitation technology, then the neroli essential oil is wrapped in the exosome, the stability of the essential oil is improved, the action time is prolonged, meanwhile, the neroli essential oil and active ingredients of the exosome generate a synergistic effect, and the antioxidant activity is jointly enhanced.

The invention provides a hole transport layer precursor solution, a hole transport layer, a preparation method and application of the hole transport layer, and a perovskite cell, and belongs to the technical field of hole transport layers. The hole transport layer precursor solution comprises a self-assembled single molecule and an organic solvent; the organic solvent comprises a solvent A, a solvent B and a solvent C; the solvent A comprises more than one of a phosphate ester solvent and an alcohol ether solvent; the solvent A contains four hydrogen bond receptors; the boiling point of the solvent A is 215-290 DEG C; the solvent B comprises more than one of ethanol, isopropanol, normal propyl alcohol, butanol, ethylene glycol and N, N-dimethylformamide; the solvent C comprises more than one of ethyl acetate and normal hexane. A ternary hydrogen bond network is formed through the solvent A, the solvent B and the solvent C, the agglomeration degree of SAM molecules is remarkably reduced, and the device performance is improved.

The invention belongs to the technical field of vehicle protection materials, and particularly relates to a coating for an explosion-proof vehicle. The coating is composed of an adhesion bottom layer, an energy-absorbing middle layer and an anti-impact outer layer, wherein the adhesion bottom layer contains epoxy resin and flaky zinc powder / mica powder, and a laminated shielding structure is formed to improve the adhesion force to be larger than or equal to 8 MPa; the energy-absorbing middle layer is a composite material of modified nano silicon dioxide / polyethylene glycol-based STF and silanized aramid fiber, the viscosity of the energy-absorbing middle layer is sharply increased by more than 50 times at the strain rate of 500s <-1 >, and 65% of explosion impact energy can be absorbed; the anti-impact outer layer adopts a polyurea elastomer to wrap gradient distribution silicon carbide microspheres, pyramid-shaped protrusions are designed on the surface, the fragment defense speed reaches 430 m / s, and the shock wave reflection dispersion is increased by 50%. The whole anti-explosion coating passes UL94V-0 certification through a synergistic flame-retardant system, the chemical protection and self-cleaning capacity is improved through a super-hydrophobic surface layer, and the problems that a traditional anti-explosion coating is poor in adhesive force, weak in composite threat resistance and insufficient in environmental adaptability are solved.

The invention discloses a multi-network anti-freezing hydrogel electrolyte, a preparation method thereof and application of the multi-network anti-freezing hydrogel electrolyte in an electrochemical device. The hydrogel is prepared by using polyvinyl alcohol (PVA) and polyacrylamide (PAM) to form a basic network skeleton, introducing phytic acid, ethylene glycol and lithium / zinc bimetal salt (Li2SO4 / ZnSO4), and carrying out thermal initiation polymerization and freeze thawing. The hydrogel prepared by the invention has a multiple physical cross-linked network formed by polymer molecular chain entanglement, hydrogen-bond interaction among functional groups and metal coordinate bonds constructed between phosphate groups and divalent metal ions, so that the hydrogel electrolyte has excellent mechanical properties. Due to introduction of ethylene glycol, formation of ice crystals is effectively inhibited, and the hydrogel is endowed with excellent anti-freezing performance; the high-concentration Li < + > and Zn < 2 + > ensure the high ionic conductivity. The supercapacitor assembled by using the hydrogel electrolyte shows relatively high specific capacitance and good capacitance retention rate under bending and freezing conditions, and has good electrochemical properties and safety performance.

The invention relates to the technical field of biological detection, and discloses a mycoplasma pneumoniae nucleic acid rapid detection method, which comprises the following steps: mixing a sample to be detected with a multifunctional pretreatment buffer solution containing tris (hydroxymethyl) aminomethane, potassium acetate, polyethylene glycol, saponin, spermine tetrahydrochloride and tris (2-carboxyethyl) phosphine hydrochloride, and carrying out cracking treatment; a cracking mixed solution is obtained; redissolving the enzymatic isothermal amplification basic reagent, the specific primer and the probe to obtain a redissolving amplification system; sucking the supernatant of the cracking mixed solution, adding the supernatant into a redissolving amplification system, and adding a magnesium acetate solution to obtain a reaction mixed solution to be detected; and carrying out isothermal amplification and signal acquisition to obtain a detection conclusion. The multifunctional pretreatment buffer solution is used for cracking the to-be-detected sample, sample liquefaction, cracking and nucleic acid release are completed in a single system, the nucleic acid extraction and purification step of centrifugal column adsorption or magnetic bead elution is avoided, and the operation process is simplified.

The invention discloses a perovskite type composite metal oxide oxygen carrier catalyst as well as a preparation method and application thereof, and belongs to the field of biomass chemical chain gasification / reforming. The oxygen carrier catalyst is of a La, Fe and Ni co-doped SrTiO3 perovskite structure, and active components Fe and Ni are embedded into a main body SrTiO3 perovskite crystal phase structure in an oxide or simple substance form; the method comprises the following steps: preparing an aqueous solution of lanthanum nitrate, strontium nitrate, nickel nitrate, ferric nitrate and citric acid, adding a mixed solution of tetrabutyl titanate and ethylene glycol into the aqueous solution, heating in a water bath, and stirring to form gel; drying and calcining the gel to obtain intermediate powder; and the intermediate powder is oxidized and reduced to form a high-temperature crystal structure under different atmospheres, and the perovskite type composite metal oxide oxygen carrier catalyst is obtained. The oxygen carrier catalyst provided by the invention has high tar conversion rate and stable cycle activity in the biomass chemical chain gasification / reforming process.

The invention discloses application of a benzoquinone-based covalent organic framework material as a bifunctional photocatalyst in a photo-assisted lithium-air battery, and the benzoquinone-based covalent organic framework material is prepared by taking cyclohexanehexone octahydrate and 2, 3, 5, 6-tetraaminocyclohexane-2, 5-diene-1, 4-diketone as raw materials, ethylene glycol as a solvent and acetic acid as a catalyst through a hydrothermal reaction. And carrying out Schiff base reaction under the protection of nitrogen atmosphere. The benzoquinonyl covalent organic framework material has a large number of donor and acceptor units, has a wide visible light absorption range, can be used as a photo-assisted lithium-air battery bifunctional photocatalyst, greatly inhibits photon-generated carrier recombination, reduces the over-potential of a photo-assisted lithium-air battery, remarkably improves the battery assembly efficiency, and has a wide application prospect. And a new direction is provided for selection of photocatalysts in the field of lithium-air batteries.

The invention discloses a method for efficiently depolymerizing polyethylene glycol terephthalate, which comprises the following steps: mixing a PET material, ethylene glycol and a core-shell type magnetic nano composite catalyst, and carrying out alcoholysis reaction at 160-200 DEG C for 30-180 minutes; after the reaction is finished, separating the catalyst from a reaction system through an external magnetic field to obtain a solution containing bis (2-hydroxyethyl) terephthalate; the core-shell type magnetic nano composite catalyst comprises a magnetic FeO core, a SiO shell layer and active metal sites, the FeO core is coated with the SiO shell layer, the SiO shell layer is an insulating inorganic layer and is of a porous structure, the active metal sites are fixed to the surface of the SiO shell layer through coordinate bonds, and active metal is selected from one or more of Co, Ni, Cu, Ce, La and Al. The problems that an existing PET alcoholysis catalyst is easy to dissolve out, difficult to separate, harsh in reaction condition and poor in cycling stability are solved.

The invention discloses a high-temperature-resistant and salt-resistant fracturing fluid and a preparation method thereof, and relates to the technical field of oil field fracturing fluids. When the high-temperature-resistant and salt-resistant fracturing fluid is prepared, sodium 3-chloro-2-hydroxypropane sulfonate, N, N-dimethylacrylamide and ethylene glycol react to prepare a quaternized solid product, and then the quaternized solid product reacts with 1-bromooctadecane to prepare an amphoteric hydrophobic monomer; guar gum powder reacts with 3-(1-naphthyloxy)-1, 2-epoxypropane to prepare naphthyloxy functionalized guar gum, and then the naphthyloxy functionalized guar gum, acrylamide and an amphoteric hydrophobic monomer are subjected to initiated polymerization through ceric ammonium nitrate to prepare modified guar gum; enabling zirconium oxychloride octahydrate, titanium chloride, lactic acid, ethanediamine and glycerol to react to prepare an organic zirconium cross-linking agent; and finally, mixing the modified guar gum, an organic zirconium cross-linking agent, sodium thiosulfate, sodium bromate, a surfactant and water to prepare the high-temperature-resistant and salt-resistant fracturing fluid. The high-temperature-resistant and salt-resistant fracturing fluid prepared by the invention has excellent high-temperature resistance and salt resistance.

The invention discloses chiral ionizable lipid nanoparticles and a preparation method thereof, and belongs to the technical field of biomedical materials. The chiral ionizable lipid nanoparticle comprises chiral amino acid derived lipid, ionizable lipid, auxiliary lipid, cholesterol, a phospholipid polyethylene glycol derivative and an RNA (Ribonucleic Acid) drug, the preparation method comprises the following steps: dissolving chiral amino acid derived lipid in methanol, respectively dissolving ionizable lipid, auxiliary lipid, cholesterol and phospholipid polyethylene glycol derivative in ethanol, and mixing to obtain a total lipid organic phase; dissolving an RNA drug in DEPC water to obtain an RNA aqueous solution, and mixing the RNA aqueous solution with an acidic buffer solution to obtain an RNA aqueous phase; quickly mixing the total lipid organic phase and the RNA water phase, and standing and incubating; adding the mixed solution into a 3500 Da dialysis bag, taking 1 * phosphate buffer solution (PBS, pH = 7.4) as an external water phase, and dialyzing to obtain the chiral ionizable lipid nanoparticles. The lipid nanoparticles provided by the invention can enhance the RNA uptake efficiency, and have good application prospects in the treatment of systemic inflammation and other diseases.

The invention provides a low-molecular soluble chelating collector as well as a preparation method and application thereof, and belongs to the technical field of mineral processing. According to the collecting agent, low-molecular-weight ethylene glycol terephthalate serves as a precursor, and isosorbide is introduced for a copolymerization reaction; glutamic acid is introduced as a branched chain unit, and the branching degree and reaction active site density of the molecular structure are remarkably improved by utilizing the polyfunctional group characteristic of glutamic acid. A rigid ring structure and an ether bond of the isosorbide endow the medicament with good water solubility and dispersity, and invalid curling of a macromolecular chain is avoided; the introduction of glutamic acid branched chains greatly increases the number of hydroxyl groups and amino groups capable of reacting with carbon disulfide, so that each molecule carries more xanthate groups, and the adsorption stability and coverage density of the molecule on the surface of arsenopyrite are enhanced. By means of the structure, xanthate functional groups are fully exposed, multi-tooth chelation is easily conducted on the xanthate functional groups and iron and arsenic ions on the surface of arsenopyrite, a strong hydrophobic surface layer is formed, and therefore the collecting selectivity is remarkably improved.

The invention discloses application of sulfur quantum dot nanoparticles to improvement of plant waterlogging resistance. The invention provides sulfur quantum dot nanoparticles PEI-SQDs prepared from sulfur, sodium hydroxide, polyethylene glycol and polyethyleneimine. The sulfur quantum dot nanoparticles PEI-SQDs are simple in synthesis method, small in particle size, low in toxicity, low in price, simple to prepare, suitable for large-scale production, good in water solubility and good in biocompatibility; the compound has the capacity of removing active oxygen and ethylene in vitro, and can remove excessive active oxygen and ethylene in plants with waterlogging stress, relieve short-term waterlogging stress suffered by crops and recover growth and development of the crops when being applied to the plants with waterlogging stress; further, long-term waterflooding stress on the crops can be relieved, and the yield of the crops is increased; and the sulfur quantum dot nanoparticles are simple and convenient in use method and obvious in action effect.

The invention discloses a UV-cured high-weather-resistance optical thin film and a preparation method thereof, and relates to the technical field of optical thin films. The optical film is prepared by taking polyethylene glycol terephthalate as a base material and coating the base material with a UV curing coating, and the UV curing coating comprises the following raw materials in parts by weight: 15-20 parts of aliphatic polyurethane acrylate, 5-8 parts of perfluorobutyl ethyl acrylate, 8-12 parts of hydroxyethyl acrylate, 6-10 parts of 1, 2, 4-trimethyl-1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 2, 4-trimethyl-1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 2, 4-trimethyl-1, the invention relates to a UV (ultraviolet)-resistant coating which is prepared from the following raw materials in parts by weight: 1-2 parts of 2, 6-hexanediol diacrylate, 5-8 parts of trimethylolpropane triacrylate, 30-40 parts of modified epoxy acrylate, 1-2 parts of a silane coupling agent KH-570, 2-3 parts of a photoinitiator 1173, 0.5-1.2 parts of a modified ultraviolet absorbent UV-327, 0.8-1.5 parts of a hindered amine light stabilizer 540, 0.3-0.8 part of an antioxidant 1010, 0.09-0.12 part of an ultraviolet absorbent Tinuvin400 and 0.2-0.5 part of polyether modified polydimethylsiloxane. According to the UV-cured high-weather-resistance optical thin film, polyethylene glycol terephthalate is used as a base material, key raw materials such as a UV-cured coating with a scientific formula, modified epoxy acrylate and the like are finely prepared, a two-stage curing process is adopted, and the weather resistance is excellent.

The invention relates to the technical field of ceramic glaze water, in particular to ceramic glaze water capable of continuously releasing negative ions based on a rare earth material and a preparation method of the ceramic glaze water. Comprising a negative ion material, sodium polystyrenesulfonate, an immobilized bacterium preparation, carbon nanotube modified graphene oxide, turbo stone, modified sepiolite, nano-zinc oxide, sodium hexametasilicate, polyethylene glycol, a composite antioxidant, a coalescing agent, a slow-release carrier and deionized water. The negative ion material is formed by mixing low-radioactivity commercial rare earth powder, tourmaline and opal according to the mass ratio of (3-4): (4-5): 1. According to the invention, the preparation cost of the glaze water is reduced and the production efficiency is improved by optimizing the composition and compounding mode of the negative ion material, enhancing the stability of the bacterial preparation and simplifying the preparation process, meanwhile, the negative ion release durability, the ceramic surface adhesive force and the antibacterial property are remarkably enhanced, and the requirements of industrial production and practical application are met.

The application belongs to the technical field of regenerated polyester, and particularly relates to a recycling method of waste polyester textiles, which comprises the following steps: decolorizing colored waste polyester textiles by using a decolorizing agent, wherein the decolorizing agent is one or more of dimethyl carbonate, diethyl carbonate and methyl ethyl carbonate; depolymerizing the decolorized polyester textiles by using a depolymerizing agent to obtain terephthalate, wherein the depolymerization rate of the decolorized polyester textiles is 98.0-100%; converting the terephthalate into DMT first, and then performing a re-polymerization reaction on the DMT, ethylene glycol, a catalyst and a functional additive to obtain regenerated PET. The application adopts a process of decolorizing first and then depolymerizing, and the decolorizing and depolymerizing are coordinated, so that the process is simplified, the energy consumption and pollution are reduced, and the economy and sustainability of the recycling of waste polyester textiles are improved.

The invention belongs to the field of separation membranes, and particularly relates to an anti-pollution and washable reverse osmosis membrane and a preparation method thereof. The reverse osmosis membrane provided by the invention is prepared according to the following steps: soaking a nascent state polyamide reverse osmosis membrane in a first treatment solution, taking out and cleaning, then soaking in a second treatment solution, taking out and draining to obtain the anti-pollution and washing-resistant reverse osmosis membrane, the nascent state polyamide reverse osmosis membrane comprises a non-woven fabric layer, a porous support layer and a polyamide separation layer which are in contact in sequence; the first treating fluid contains double-end amino polyethylene glycol and triethylamine; the second treatment liquid contains polyvinyl alcohol and alpha-aldehyde group-omega-carboxyl polyethylene glycol. Experimental results show that the reverse osmosis membrane provided by the invention has relatively high anti-pollution capacity, desalting rate and acid and alkali cleaning resistance.

The invention provides a polyethylene glycol derivative-collagen cartilage repair gel which is characterized by being prepared from the following components in parts by weight: 8 to 12 parts of collagen (namely COL) solution, 0.5 to 2 parts of polydeoxyribonucleotide (namely PDRN), 4 to 8 parts of polyethylene glycol disuccinimide succinate (namely SS-PEG-SS) solution and 0.1 to 0.4 part of tannic acid (namely TA), and particularly discloses a preparation method and application of the polyethylene glycol derivative-collagen cartilage repair gel. In a word, the composite gel and the collagen are subjected to efficient amidation reaction through SS-PEG-SS to form a stable three-dimensional network, so that the structural support of the type I collagen, the tissue repair of PDRN and the anti-inflammatory and anti-oxidation characteristics of tannic acid are successfully integrated; therefore, the composite material has the comprehensive performance of good structural stability, high mechanical strength, good biocompatibility, controllable degradation period, excellent needle passing performance and the like, and shows the wide application prospects of clear repair effect, remarkable component synergistic effect, mature production process, outstanding cost effectiveness and the like.

The invention relates to a doxepin hydrochloride tablet. The doxepin hydrochloride tablet is prepared from doxepin hydrochloride, polyethylene glycol 6000, a filling agent, a disintegrating agent, a flow aid and a lubricating agent. The preparation method comprises the following steps: heating and melting polyethylene glycol 6000, adding a doxepin hydrochloride raw material according to a prescription proportion, and uniformly stirring and mixing; and after complete melting, rapidly cooling and solidifying to form a solid dispersion. And after curing, drying in a drying oven, crushing and sieving. And uniformly mixing the crushed particles with the filler and the lubricant, and directly tabletting. The doxepin hydrochloride has high hygroscopicity, is unstable to damp and heat and easily generates a large amount of impurities under strong oxidation conditions, the doxepin hydrochloride is firstly prepared into a solid dispersion and then is directly compressed, so that the medicine is highly dispersed in a carrier material in the states of molecules, colloids, amorphous forms, microcrystals and the like, and the effect of wrapping the medicine is achieved by controlling the ratio of the medicine to the carrier. Direct contact between the medicine and air is avoided, so that the problems of hygroscopicity and instability of the medicine are solved, and the product stability is improved.

The invention provides a gold ore phase analysis method, and belongs to the field of mineral analys.The gold ore phase analysis method comprises the steps that a gold ore sample is prepared into ore pulp, the pH value is adjusted to 10-11, ultrasonic cavitation treatment is conducted after polyethylene glycol is added, and limonite turbid liquid and sedimentation bottom mud are obtained through separation; the turbid liquid is subjected to flocculation precipitation, drying, roasting, acid dissolution and impurity removal, and the limonite gold-loaded grade is obtained through the mass difference before and after dissolution and gold concentration determination; separating metal sulfide ore heavy minerals and gangue minerals from the settled bottom mud through artificial heavy elutriation, performing acid dissolution and impurity removal on the metal sulfide heavy minerals, and calculating the gold loading grade of the metal sulfide heavy minerals through mass difference and gold concentration determination; after gangue minerals are subjected to oxidizing roasting, the gold content is measured after concentrated acid dissolution; and calculating the distribution rate of gold based on the result. The gold loading grade and distribution of the limonite phase, the metal sulfide ore phase and the gangue mineral phase are measured in a split-phase mode, the method is highly matched with the gold ore development process, operation is easy and convenient, the result is reliable, and beneficiation and metallurgy technological process formulation and technical index pre-judgment can be effectively served.

The invention relates to the field of material chemistry on-line detection, in particular to a 1, 2, 4-trichlorobenzene on-line detection material and a preparation method thereof, and provides a film-forming sensitive layer material capable of being coated on the surface of a transducer, and the film-forming sensitive layer material comprises chitosan, a crosslinking component with the content of 0.1-5wt% in terms of glutaraldehyde and magnetic core-shell molecularly imprinted particles after being dried, the magnetic core-shell molecularly imprinted particle contains a ferroferric oxide magnetic inner core, a silicon dioxide middle layer and a molecularly imprinted polymer shell layer, and the shell layer is a cyclodextrin methacrylate and ethylene glycol dimethacrylate copolymer network and takes 1, 2, 4-trichlorobenzene as a template. The material keeps the membrane integrity and long-term stability under the working conditions of circulation and regeneration and also gives consideration to quick response, and the residual 1, 2, 4-trichlorobenzene is controlled to be not greater than 0.10 wt% and the residual glutaraldehyde is controlled to be not greater than 0.5 wt%. The method is used for relieving structural mass transfer contradiction and processing and coating coupling contradiction caused by high filler load, and has online detection application value.

The invention belongs to the field of PET (polyethylene glycol terephthalate) plastic waste treatment, and particularly relates to preparation of a copper oxide-nickel hydroxide core-shell structure catalytic material and application of the copper oxide-nickel hydroxide core-shell structure catalytic material to preparation of high-added-value formic acid by upgrading electro-catalysis PET plastics, and the preparation method comprises the following steps: (1) placing a copper conductive substrate in an alkali etching mixed solution for alkali etching treatment, obtaining a conductive substrate on which a Cu (OH) 2 precursor grows; (2) placing the conductive substrate on which the Cu (OH) 2 precursor grows in a muffle furnace for heat treatment to obtain a conductive substrate on which CuO nanowires grow; and (3) placing the conductive substrate on which the CuO nanowire grows in a hydrothermal kettle, and obtaining the CuO-coated Ni (OH) 2-x core-shell structure catalyst through a hydrothermal method.

The invention discloses a moisture absorption and sweat releasing polyester fiber and a preparation method and application thereof, and relates to the field of polyester fibers. The moisture absorption and sweat releasing polyester fiber is prepared from the following raw materials in parts by weight: 85 to 95 parts of fiber-grade PET polyester, 4 to 12 parts of PET copolymer, 0.5 to 2.0 parts of dispersing agent and 0.1 to 0.5 part of antioxidant, wherein the PET copolymer is prepared from the following raw materials: terephthalic acid, ethylene glycol, neopentyl glycol, a catalyst and polyethylene glycol. On the basis of terephthalic acid and ethylene glycol, neopentyl glycol and polyethylene glycol are further added, the formed PET copolymer serves as a moisture absorption and sweat releasing modifier and is subjected to melt blending and spinning with fiber-grade PET polyester, hydrophilic groups and a fiber structure are fused into a whole, the moisture absorption and sweat releasing performance of the prepared polyester fiber is improved, and the moisture absorption and sweat releasing effects of the polyester fiber are improved. The durability of the moisture absorption and sweat releasing performance is also ensured.

The present invention relates to a packaged condom comprising a sealed package; and within the package, a condom comprising natural rubber latex and / or synthetic polyisoprene; wherein the condom comprises, on one or more surfaces thereof and in contact with the natural rubber latex and / or synthetic polyisoprene, an aqueous lubricant; wherein the aqueous lubricant comprises: a thickener and 5 wt.% to 30 wt.%, based on the total weight of the aqueous lubricant, of a humectant comprising at least one organic compound selected from the group consisting of glycerol, propylene glycol, polyethylene glycol, and any combination thereof; and one or more sugar alcohols having a molecular weight of from 120 to 10000 g / mol. It also relates to a method for preparing a packaged condom and to the use of an aqueous lubricant to lubricate one or more surfaces of a condom. The condom preferably presents a transparent appearance to the end user.

The invention discloses an optical paste film and a preparation method thereof, and relates to the technical field of optical functional materials. The optical slurry film is prepared by taking a polyethylene glycol terephthalate film as a base material and coating an optical slurry coating, the optical slurry coating is prepared from the following raw materials in parts by weight: 12 to 16 parts of nano silicon dioxide, 22 to 28 parts of acetone and butanone mixed solvent, 7 to 9 parts of modified titanium dioxide, 4 to 6 parts of nano zirconium oxide, 30 to 35 parts of modified epoxy resin, 18 to 22 parts of butyl acrylate, 4 to 6 parts of dioctyl sebacate, 2.5 to 3.5 parts of silane coupling agent KH-570, 1 to 1.5 parts of organic silicon flatting agent and 0.6 to 1 part of organic silicon defoaming agent. 1.2-1.8 parts of an antioxidant 1010, 3-4 parts of a photoinitiator 184 and 6-8 parts of bis (4-tert-butylphenyl) iodine hexafluorophosphate; the polyethylene glycol terephthalate film pretreatment material comprises absolute ethyl alcohol and deionized water. The raw materials are scientifically proportioned, the titanium dioxide and the epoxy resin are clearly modified, the preparation process is complete, and the finished product is high in light transmittance, good in weather resistance, adaptive to the requirements of the optical field and high in practicability.

Disclosed is a process for hydrolytic depolymerization of a polyamide contained in a chemical feedstock F, wherein the process comprises: providing the chemical feedstock F; providing a liquid aqueous stream SW; preparing a mixture comprising the raw material F and the liquid aqueous stream SW and subjecting said mixture to polyamide 6 depolymerization conditions in a chemical reaction unit UR, thereby obtaining an aqueous stream SE exiting the UR, the stream SE comprising epsilon-caprolactam, wherein the mixture to be subjected to polyamide 6 depolymerization conditions comprises polyamide 6 and further comprises polyethylene terephthalate and polyamide 6.6 in a mass ratio rS = (mPA6.6 + mPET) / mPA6, wherein 0.01 < = rS < = 2.5.