444 results about "Phosphorous acid" patented technology

The invention discloses a wear-resistant vehicle body film and a preparation method thereof, and relates to the technical field of films. The wear-resistant automobile body film prepared by the invention is prepared from polytetrahydrofuran ether glycol, isophorone diisocyanate, a catalyst, dihydric alcohol quaternary ammonium salt, a functional aid, modified silicon dioxide and a chain extender. The dihydric alcohol quaternary ammonium salt is obtained by reacting N, N '-dihexyl-N, N'-dimethyl propane-1, 3-diamine with monochloroacetone and then condensing with glycerol; the functional additive is obtained by reacting 2-boric acid thiophene-4-methyl acetate with 2, 7-dibromofluorene and then carrying out bromination hydrolysis; the modified silicon dioxide is obtained by reacting pretreated silicon dioxide with melamine and then reacting with sodium hypophosphite. The wear-resistant vehicle body film prepared by the invention has good anti-aging, wear-resistant, antibacterial and flame-retardant properties.

The invention discloses hydrolysis-resistant liquid phosphite ester and a preparation method and application thereof.The hydrolysis-resistant liquid phosphite ester is prepared by the steps that 2, 2, 4-trimethyl-1, 3-pentanediol and phosphorus trichloride or phosphite triester serve as raw materials, a cyclization reaction is conducted firstly, and then the hydrolysis-resistant liquid phosphite ester is obtained; and then carrying out nucleophilic substitution on Cl or aryl and alkyl on the cyclized intermediate by using higher saturated monohydric alcohol with more than C8, wherein the molecular structure is as shown in formula I in the specification. The liquid phosphite ester is novel liquid phosphite ester, the main body of the liquid phosphite ester is of a six-membered ring structure, the basic structure of the phosphite ester is reserved to the maximum extent, and the anti-oxidation effect of the phosphite ester is guaranteed; hydrophobic aliphatic chain structures on phosphorus atoms and branched chains of the phosphorus atoms prevent water molecules from approaching P-O bonds, so that the phosphorus atoms and the branched chains are prevented from being attacked by the water molecules, and the hydrolysis resistance is improved under the conditions that any additional amine hydrolysis-resistant agent is not used and any steric hindrance group is not introduced; good practical value, economic value and market prospect are realized.

The invention discloses a synthesis method of allyl phosphonic acid diester. According to the method, phosphorous acid diester and an allyl chloride compound are used as raw materials and react in the presence of a specific transition metal catalyst and alkali under the conditions of normal pressure and 45-60 DEG C to obtain the allyl phosphonic acid diester. The method has the advantages of mild reaction conditions, simple operation, high product yield (90-99%), no by-product, no generation of halogenated alkane gas and easy industrial production, and is suitable for the fields of polymer flame retardants, electronic materials, pesticide and medicine intermediates and the like.

The invention discloses a CAD detection method for phosphoric acid and phosphorous acid in an alendronate sodium oral solution, and belongs to the technical field of pharmaceutical analysis. The method comprises the following steps: preparing a reference stock solution and a test solution; then setting high performance liquid chromatography detection conditions; a Shodex VN-504D chromatographic column is adopted, a CAD detector is adopted as a detector, a mixed solution of a mobile phase A and a mobile phase B is adopted as a mobile phase, the mobile phase A is ammonium formate, the mobile phase B is an acetonitrile solution, and gradient elution is performed by adopting the mobile phase; and respectively measuring the reference stock solution and the test solution, injecting into a liquid chromatograph, and recording a chromatogram. A CAD detector is adopted, the detection sensitivity is obviously improved, the quantitative concentration can reach 0.24 mu g / mL, and the detection concentration can reach 0.10 mu g / mL. The method is high in specificity, high in sensitivity, good in durability, rapid, simple, effective and reliable.

The invention discloses a flame-retardant cotton fiber and a preparation method thereof, and relates to the field of cotton fibers. When the flame-retardant cotton fiber is prepared, dicarboxyl phenyl porphyrin and copper nitrate react to prepare a metal organic framework nanosheet; the preparation method comprises the following steps: reacting 2, 4, 6-tri (4-formyl phenyl)-1, 3, 5-triazine, 2-aminomethyl piperazine and phosphorous acid to prepare a flame-retardant graft; the cotton balls, the metal organic framework nanosheets and the flame-retardant graft react to prepare pre-modified cotton fibers; and carrying out ring-opening reaction on the pre-modified cotton fiber and epoxy chloropropane, and then carrying out ring-closing to obtain the flame-retardant cotton fiber. The flame-retardant cotton fiber prepared by the invention has excellent antibacterial property, flame retardance, color fixation and dispersity.

The invention discloses a novel phosphorus-containing macromolecular flame retardant and a preparation method and application thereof, the flame retardant is a polymer with a general formula (I), the main chain of the flame retardant is composed of an olefin-containing phosphonate structural unit, and the side chain R2 is a phosphonate group or a phosphonate metal salt group. The preparation method comprises the following steps: firstly, carrying out reaction on trialkyl phosphite and halogenated olefin containing active groups to efficiently prepare a functional monomer containing polymerizable double bonds and phosphonate side chains; then carrying out free radical polymerization to obtain a macromolecular polymer; the phosphonate can be further partially or completely hydrolyzed and complexed with multivalent metal ions to form the flame retardant with an ionic cross-linked structure. The macromolecular flame retardant is high in phosphorus content, good in thermal stability and excellent in compatibility with a polymer matrix, can play a flame-retardant role in a condensed phase and a gas phase at the same time, and effectively overcomes the problems that a micromolecular flame retardant is easy to migrate and poor in durability, and the mechanical property of a matrix material is reduced. The preparation method is efficient, controllable and suitable for continuous production.

The invention provides a high-performance polyamide flame-retardant composite material based on element synergistic effect and a preparation method thereof, and belongs to the technical field of polyamide flame-retardant materials. The preparation method comprises the following steps: preparing a phosphorus-nitrogen flame retardant, preparing a surface-modified rare earth-silicon-based material, preparing a mixture, extruding and granulating. The step of preparing the mixture comprises the following steps: uniformly mixing brominated polystyrene (BPS), a phosphorus-nitrogen flame retardant, a rare earth-silicon-based material, glass fibers, an antioxidant 1098, a heat stabilizer diisooctyl phenyl phosphite, nylon 66 and nylon 6 to obtain the mixture; according to the invention, the use of antimony oxide in the traditional bromine-antimony flame-retardant system preparation process is abandoned, and the preparation process is simple, good in repeatability, green, environment-friendly and efficient.

The invention provides epoxy resin for halogen-free flame-retardant self-leveling powder coating and a preparation method of the epoxy resin, and belongs to the technical field of powder coating. The flame retardant is mainly prepared from anhydrous piperazine, bisphenol A diglycidyl ether, trihydroxymethyl phosphorus oxide, triethyl phosphite, epoxy chloropropane, sodium hydroxide, N-methyl iminodiacetic acid, ethylene glycol diglycidyl ether and other main raw materials through polymerization. The prepared epoxy resin and 2-phenylimidazoline are subjected to low-temperature curing (135 DEG C / 20 min) on the premise that an additional flatting agent does not need to be used, the flexibility of a coating film is good, the impact resistance grade is high, the impact performance reaches the condition that no cracking phenomenon exists in the front and back 60cm, the leveling grade reaches the grade 7 or above, the gloss is high and reaches 95% or above, the oxygen index reaches 34% or above, and the halogen-free flame retardant performance is excellent.

The invention discloses an oligonucleotide synthesis process of a sulfo-PMO structure. In the oligonucleotide synthesis process of the sulfo-PMO structure, the molecular structural formula of sulfo-PMO is shown in the specification. According to the invention, the molecular structure of thio-PMO is specifically limited, and the synthesis of nucleotide phosphate amide and (thio) phosphoric acid amide in the solid-phase synthesis oligonucleotide is carried out along the direction from 5'to 3 ', that is, in each cycle period, the O5'or O6' position of the nucleotide phosphate amide and (thio) phosphoric acid amide monomer is firstly subjected to coupling reaction, and then the protecting group is removed at the O3 'or N3' position, so that the oligonucleotide phosphate amide and (thio) phosphoric acid amide are obtained. And releasing active hydroxyl or amino / amido to enter the next cycle. The protecting group adopted by the sulfo-PMO molecule is consistent with the protecting groups of other nucleotides, so that the conversion rate of each step of coupling reaction can be conveniently detected on line.

The invention relates to the technical field of films, in particular to a PFAS-free high-flame-retardant polycarbonate film and a preparation method thereof, and the PFAS-free high-flame-retardant polycarbonate film comprises the following raw materials by mass: 70-85% of PC resin; 0.5-3% of a silicon flame retardant; 4-8% of a phosphorus-based flame retardant; 5-10% of talcum powder; 5-10% of a low-temperature sintering agent; 0.05 to 0.2 percent of an antioxidant 168; 0.05 to 0.2 percent of an antioxidant 1010; 0.1-0.3% of lubricant silicone oil; and 0.05-0.2% of a 70% phosphorous acid solution.

The invention discloses a low-smoke halogen-free environment-friendly flame retardant, and relates to the technical field of flame retardants. The invention discloses a low-smoke halogen-free environment-friendly flame retardant. The graphene quantum dot composite material is prepared from the following raw materials in parts by weight: 8 to 12 parts of novel phosphorus-nitrogen heterocyclic compound, 5 to 9 parts of silane-terminated polyether, 2 to 5 parts of graphene quantum dot dispersion liquid, 6 to 10 parts of pentaerythritol diphosphate melamine salt, 5 to 8 parts of melamine cyanurate, 3 to 6 parts of zinc borate, 8 to 12 parts of magnesium hydroxide, 10 to 15 parts of ammonium polyphosphate, 3 to 7 parts of modified polycarbonate and 4 to 8 parts of aluminum diethylphosphinate. The invention relates to a high-temperature-resistant anti-aging coating which is prepared from the following components in parts by weight: 2-4 parts of an organic silicon elastomer, 0.2-0.5 part of triphenyl phosphate, 0.3-0.6 part of polyethylene wax, 0.3-0.8 part of a silane coupling agent KH-550 and 25-35 parts of deionized water. The low-smoke halogen-free environment-friendly flame retardant disclosed by the invention has remarkable advantages, adopts various environment-friendly raw materials, and is green, safe and free of halogen pollution. Through the unique formula design, all the components have a synergistic effect, the flame retardant property is excellent, and the fire risk can be effectively reduced. The added graphene quantum dots and other components also improve the thermal stability and mechanical properties of the product, and the application prospect is wide.

The invention discloses a preparation method of an antibacterial warm-keeping fabric, and relates to the technical field of textiles. When the antibacterial warm-keeping fabric is prepared, firstly, (E)-butyl-2-ene-1, 4-diamine, glyoxal, formaldehyde and butyric acid are used as raw materials to synthesize a polyimidazolium salt antibacterial agent, then the polyimidazolium salt antibacterial agent is copolymerized with polytetrahydrofuran ether glycol and diphenylmethane diisocyanate to prepare an antibacterial polyurethane spinning solution, and the antibacterial fabric is obtained through wet spinning and weaving. The preparation method comprises the following steps: reacting L-cysteine with 3-amino propyl triethoxy silane to prepare cysteamine acyl propyl triethoxy silane, reacting with formaldehyde and phosphorous acid to obtain flame-retardant modified silane, and further preparing a silicon dioxide solution from the flame-retardant modified silane and sol-gel such as methyltrimethoxysilane; finally, the antibacterial fabric is treated with a benzophenone solution and then soaked with a silicon dioxide solution, and the antibacterial thermal fabric is prepared through ultraviolet irradiation, standing gelation, aging and hexane washing. The prepared fabric has excellent antibacterial property, heat retention property and flame retardant property.

The preparation method comprises the following steps: sequentially carrying out esterification reaction and polycondensation reaction on terephthalic acid, ethylene glycol, equol or a derivative thereof in the presence of the catalyst to generate the modified polyester, wherein the catalyst is prepared by enabling antimony trioxide, stannous octoate, tetrabutyl titanate and triphenyl phosphite to react in a solvent at the temperature of 100 DEG C or above; the modified polyester prepared by the method has relatively high intrinsic viscosity and fracture tensile strength, can meet the application requirements of special high polymer materials, and solves the problem that the application of semi-biomass PET copolyester in the field of special high polymer materials is limited in the prior art.

The invention provides halogen-free flame-retardant liquid epoxy resin, solid epoxy resin for powder coating and a preparation method of the solid epoxy resin, and belongs to the technical field of powder coating. The liquid epoxy resin disclosed by the invention is prepared by polymerizing 2, 4-diamino-6-phenyl-1, 3, 5-triazine, formaldehyde, triethyl phosphite, epoxy chloropropane, sodium hydroxide, DMF (Dimethyl Formamide) and the like. The contents of halogen-free flame-retardant elements nitrogen and phosphorus in the product are high, a solid epoxy resin product obtained by carrying out chain extension on liquid epoxy resin serving as a synthetic monomer of solid epoxy resin of the powder coating and bisphenol F is good in flame retardance, the oxygen index reaches 37% or above, and the flame retardance is high. A coating film obtained after the powder coating and an accelerated dicyandiamide curing agent are subjected to low-temperature rapid curing (150 DEG C / 10 min) is high in gloss and leveling grade and good in impact resistance, hardness and the like, and the application requirements of the powder coating are met.

The invention discloses a method for dehalogenation reduction of electron-rich aryl halide, which comprises the following step: by taking aryl halide as a raw material, carrying out heating reaction in the presence of phosphorous acid, elemental iodine and a solvent to prepare a corresponding aromatic compound. According to the method, the defect that expensive transition metal catalysts and equivalent metal reagents need to be used for participation in current mainstream methods is directly avoided, the electron-rich aryl halide is subjected to one-step dehalogenation reduction to obtain the corresponding aromatic hydrocarbon by taking low-cost, low-toxicity and relatively stable phosphorous acid as a reducing agent and taking the iodine elementary substance as a catalyst, and the method has the advantages of no metal participation, simple operation, low cost and the like. The method has the advantages of simple operation, low cost, environmental protection and the like, avoids the use of a metal reagent and the limitation that special equipment is not easy to amplify production, after the phosphorous acid reaction is finished, byproducts are generally phosphoric acid and corresponding phosphorus salts thereof and can be quickly removed by washing, the post-treatment is simple, and the method is beneficial to industrial production.

The invention provides a temperature-resistant and salt-resistant polymer viscosity reducer for a drilling fluid and a preparation method of the temperature-resistant and salt-resistant polymer viscosity reducer. The phosphine-containing polymer viscosity reducer can be prepared from a carboxylic acid group-containing monomer, a sulfonic acid group-containing monomer, a phosphine-containing compound and phosphorous acid through a polymerization reaction; the carboxylic acid group-containing monomer is selected from one or more of acrylic acid, methacrylic acid and maleic acid, and the sulfonic acid group-containing monomer is selected from 2-acrylamido-2-methylpropanesulfonic acid or 2-acryloyloxy-2-methylpropanesulfonic acid; the phosphine-containing compound is selected from any one of ethylene diamine tetra (methylene phosphonic acid), 1-hydroxyethylidene-1, 1-diphosphonic acid and amino trimethylene phosphonic acid. The obtained phosphine-containing polymer viscosity reducer with the corresponding structure is good in temperature resistance and salt resistance, salt resistance reaches saturation, and under the conditions of high temperature and salt pollution, the viscosity reducer still has a good viscosity reduction effect and has good temperature resistance and salt resistance; and moreover, reaction raw materials in the preparation are few, the synthesis process is simple, the cost performance is relatively high, and application is facilitated.

The invention relates to the technical field of wastewater treatment, in particular to a multi-stage circulating filtration system and method based on triphenyl phosphate production wastewater, and the system comprises a first-stage filtration system, a second-stage filtration system, a third-stage filtration system, a front-end wastewater collection tank and a flow pump, the front ends of the first-stage filtration system, the second-stage filtration system and the third-stage filtration system are connected with a three-way pipe through the flow pump, and the three-way pipe is mounted at the lower end of an anti-precipitation unit; the upper end of the anti-precipitation unit is fixedly connected with a front-end wastewater collection tank, an air source assembly is mounted on the inner side of the upper end of the front-end wastewater collection tank, and a telescopic air pipe is mounted at the lower end of the air source assembly; the anti-precipitation unit comprises a stirring box, one end of the stirring box is fixedly connected with a side end liquid discharging pipe through screws, a liquid discharging hole is formed in the middle of the bottom end of the stirring box, a stirring assembly is installed in the stirring box, and stirring blades are installed on the outer side of the stirring assembly. According to the invention, the air source assembly is driven by the liquid level change of the collecting box, the air pressure is used as power, the operation of the stirrer and the action of the cleaning scraper are automatically controlled in a linkage manner, stirring as required is realized, and energy is remarkably saved.

A method for converting post-consumer recycled (PCR) flakes of polyethylene terephthalate (PET) to pellets as part of a container recycling procedure, the method including: adding triphenyl phosphite antioxidant to a reactor at a concentration of 0.05 wt.% to 0.15 wt.%; coating the PCR flakes with the triphenyl phosphite in the reactor; and converting the PCR flakes to the pellets in an extruder after coating the PCR flakes with the triphenyl phosphite to reduce yellowing of the pellets during the conversion.

The application provides a preparation method of a rare earth metal adsorption and separation resin and a resin extraction column. The preparation method comprises the following steps: adding an oil phase composed of styrene, divinylbenzene, a pore former and an initiator into an aqueous phase containing a dispersant and an inorganic salt to perform suspension polymerization, so as to obtain a white ball resin; performing phthalimide and hydrolysis on the white ball resin, so as to obtain a primary amine resin; performing reaction on the primary amine resin with chloroacetic acid and an alkaline medium, so as to perform carboxymethylation on part of the primary amine sites; and performing reaction on the obtained intermediate resin with phosphorous acid, formaldehyde and an acidic medium, so as to perform phosphonic acid methylation on the remaining part of the primary amine sites. The white ball resin is first subjected to amination, and then part of the carboxymethylation and part of the phosphonic acid methylation are sequentially performed, so that the carboxyl type chelation sites and the phosphonic acid type chelation sites are simultaneously reserved in the same resin bead, thereby being beneficial to improving the comprehensive adsorption performance and separation performance of the resin on the rare earth metal.

The application discloses a platinum complex with controllable activity and a preparation method and application thereof, which is formed by coordination of vinyl siloxane, modified ligand and chloroplatinic acid; the modified ligand is prepared by reaction of maleic anhydride, allylamine and hydroxymethyl dimethyl phosphite. The application introduces amide groups and phosphite groups into the molecular chain of maleic anhydride, uses the groups as coordination compounds to coordinate with vinyl siloxane and platinum, and can improve the normal-temperature storage stability of the platinum catalyst while still keeping high catalytic activity of the platinum catalyst on the hydrosilylation reaction; when the platinum complex is used for catalyzing preparation of addition-type liquid silicone rubber, no inhibitor needs to be added, and the silicone rubber has good mechanical properties.

The invention relates to a synthesis method of low-cost environment-friendly dioscorea element I. The synthesis method comprises the following steps: by taking 3, 5-dimethoxybenzyl alcohol as a raw material, brominating, reacting with triethyl phosphite and 4-benzyloxy-3-methoxybenzaldehyde to generate 3, 4 ', 5-trimethoxy-3'-benzyloxy stilbene, carrying out ultraviolet cyclization reaction, reacting with palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon, palladium-carbon and debenzylating with hydrogen to obtain the Chinese yam element I. The potassium iodide is used as the catalyst in the ultraviolet lamp irradiation catalytic ring closing reaction, the pure water is used as the detergent, compared with the method adopting iodine as the catalyst and adopting a sodium thiosulfate aqueous solution as the detergent, the product yield of the compound 33-4 is 75%, the yield of the compound 33-5 is 16.6%, the purity is 98.7%, and the method has the advantages of low cost, high yield, few impurities and the like.

A method for recycling catalytic metals comprising: collecting a plurality of spent catalytic metals, wherein the spent catalytic metals contain cathodes of NMC111, NMC622, NMC811, NCA, LCoO2, LiNi0.5Mn1.5O4, LiMnO4, LiNiO2, LiMn2O4, and / or LiMnO2 compositions; subjecting the plurality of spent catalytic metals to a green mixture, wherein the green mixture includes dihydrogen phosphite and water, phosphoric acid and water, sulfuric acid and water, hydrogen chloride and water, or nitric acid and water, at temperatures of between 80 and 120° C. to form a metal leachate solution; and recovering lithium (Li) from the metal leachate solution.

The invention relates to an additive composition comprising primary anti-oxidants and a secondary anti-oxidant, wherein the primary anti-oxidants are a phenyl phosphite and 3,3′-thiodipropionic acid dioctadecylester, and wherein the secondary anti-oxidant is epoxidized soybean oil. The invention additionally relates a bituminous composition comprising primary anti-oxidants and a secondary anti-oxidant, wherein the primary anti-oxidants are a phenyl phosphite and 3,3′-thiodipropionic acid dioctadecylester; and wherein the secondary anti-oxidant is epoxidized soybean oil. The invention also relates to an asphalt composition comprising the bituminous composition with resistance to short-term and long-term chemical ageing. The invention further relates to the use of an additive composition to reduce short-term and long-term chemical ageing of a bituminous composition.

The invention discloses a microbial composition for preventing and treating vomitoxin as well as a preparation method and application of the microbial composition. The microbial composition for preventing and treating vomitoxin is mainly prepared by mixing a component I and a component II according to a mass ratio of (50.0-0.1): (50.0-99.9), the component I comprises trichoderma harzianum powder, trichoderma asperellum powder and penicillium bayi powder; and the component II comprises potassium phosphite, alkene potassium phosphate and potassium tripolyphosphate. The preparation method comprises the following steps: adding the component I and the component II into a stirrer, and stirring and mixing to obtain the coating. The invention also discloses an application of the microbial composition for preventing and treating vomitoxin. The microbial composition disclosed by the invention can generate metabolites with a biocontrol effect, has efficient inhibitory activity on fusarium, can reduce generation of vomitoxin, can effectively regulate diversity of soil microorganisms, realizes crop yield increase and soil improvement, and is green and environment-friendly. The method and application are simple, the cost is low, and the method is suitable for agricultural application.

The invention discloses a hydroxymethyl phosphonate flame retardant and a preparation method and application thereof.The method comprises the steps that phosphorus trichloride and epoxide serve as starting raw materials and react in the presence of a catalyst to generate trichloro alkyl phosphite, the obtained triester structure is dropwise added into phosphorous acid, heat preservation reaction is conducted, and dichloro alkyl phosphite is obtained; and adding a catalyst 2 into the diester product, heating, slowly adding paraformaldehyde, and continuously reacting to obtain the hydroxymethyl phosphate flame retardant. The method is low in cost, mild in reaction condition, solvent-free, capable of being efficiently completed without extreme conditions, high in reaction speed and high in conversion efficiency, is compatible with existing chemical production equipment, and provides a solid foundation for large-scale industrial production.

The application discloses a kind of superdispersion flame-retardant engineering plastic master batch and preparation method thereof, it is related to functional plastic technical field, including functional master batch, the functional master batch includes the following components by weight parts: nylon 6 sheet 100 parts, modified carbon nanotube 0.5-8 parts, diethyl phosphinic acid ethyl aluminum 5-15 parts, flame retardant 5-15 parts, carbon forming agent 2-5 parts, epoxy silicon dioxide 0.5-5 parts, compatible agent 0.5-5 parts.The application introduces diethyl phosphinic acid ethyl aluminum and flame retardant, forms carbon layer on the material surface when plastic master batch burns, and the interaction between the molecular chains of plastic master batch is improved by Schiff base structure, realizes the double performance improvement of plastic master batch flame retardant and anti-dripping, solves the problem of fire spread caused by melt dripping.

The invention relates to the technical field of pesticide synthesis processes, in particular to a one-pot multi-component preparation method of a chiral Dufulin compound. The method comprises the following steps: mixing quinine, substituted benzyl bromide and a solvent, and refluxing to obtain a reaction solution; the preparation method comprises the following steps: mixing 2-amino-4-methylbenzothiazole, 2-fluorobenzaldehyde, a solvent and a catalyst, and then refluxing to obtain a reaction system; mixing the reaction system with diethyl phosphite, the reaction liquid and an alkali reagent, and stirring to react, so as to obtain a stirred reaction material; and extracting the stirred reaction material with an extraction liquid, separating the liquid to obtain an organic phase, washing the organic phase with water, and removing the solvent to obtain the chiral Dufulin compound. According to the invention, low-cost clean synthesis of chiral Dufulin is realized; the preparation method disclosed by the invention is reasonable in design, mild in reaction condition, easy to obtain raw materials, convenient to operate, high in product yield, suitable for large-scale production and good in industrial replicability.

The application relates to the field of polyolefin fibers, and discloses a reinforced polyolefin resin composite fiber and a preparation method thereof, wherein the composite fiber is prepared from high-density polyethylene, ultra-high molecular weight polyethylene powder, modified nano silicon dioxide, modified multi-walled carbon nanotubes, polyethylene grafted maleic anhydride compatilizer, antioxidant tris(2,4-di-t-butylphenyl) phosphite and antioxidant tetra[beta-(3,5-di-t-butyl-4-hydroxyphenyl) propionic acid] pentaerythritol ester; the modified multi-walled carbon nanotubes are prepared from multi-walled carbon nanotubes, concentrated nitric acid solution and hexadecyl trimethyl ammonium bromide aqueous solution; and the modified nano silicon dioxide is prepared from nano silicon dioxide, gamma-(methacryloyloxy) propyl trimethoxysilane, acetic acid and ethanol aqueous solution. The composite fiber has good wear resistance, antistatic property and mechanical property.

The invention relates to a process for the production of a mixed P═O / P═S backbone oligonucleotide comprising a selective oxidation of an intermediary phosphite triester compound of formula I into a phosphodiester compound of formula II according to the scheme with an oxidation solution obtained by mixing iodine, an organic solvent and water, characterized in that the oxidation solution has been aged for a time period that is sufficient to selectively oxidize the phosphite triester compound of formula I into the phosphodiester compound of formula II without oxidizing the phosphorothioate internucleotide linkages.

The present application belongs to the technical field of cable material, and particularly relates to a resin composition, a cable insulation material, a cable and a preparation method. The resin composition comprises polyethylene, a crosslinking agent and a crosslinking aid. The crosslinking agent is selected from one or more of triallyl isocyanurate, trimethylolpropane trimethacrylate and trimethylolpropane triacrylate. The crosslinking aid is selected from one or more of triphenyl phosphite, dipropylene glycol diacrylate and tetraethylene glycol diacrylate. The cable insulation material made of the resin composition has a high irradiation crosslinking rate, which can significantly improve the irradiation processing speed of the subsequent cable and improve the cable output efficiency. In addition, the cable insulation material has good aging resistance, can meet the long service life requirement, saves the cable update cost and has good economic benefits.