2393 results about "Borinic acid" patented technology

The invention provides a silicon-carbon negative electrode material and a preparation method thereof. The preparation method comprises the following steps: a) mixing a phenol monomer, an aldehyde solution, ammonia water and water, dropwise adding a boric acid solution for reaction, and curing to obtain boron-containing phenolic resin; b) carbonizing the boron-containing phenolic resin obtained in the step a), mixing with alkali, and activating to obtain boron-doped porous carbon; and c) carrying out silicon deposition on the boron-doped porous carbon obtained in the step b) by adopting a gaseous silicon source, carrying out carbon coating by adopting a gaseous carbon source, and cooling to obtain the silicon-carbon negative electrode material. Compared with the prior art, the preparation method provided by the invention has the advantages that a conductive network can be formed by doping the boron element, the electron concentration can be improved, the electron transfer rate is favorably improved, the conductivity of the material is effectively enhanced, and the rate capability of the negative electrode material is effectively improved; meanwhile, the residual carbon rate in the porous carbon preparation process can be greatly increased, and the cost of the whole silicon-carbon negative electrode material is effectively reduced.

The invention belongs to the technical field of flame-retardant materials, and particularly relates to a phenylboronic acid-based P / N / B-containing halogen-free flame retardant, a preparation method thereof and application of the phenylboronic acid-based P / N / B-containing halogen-free flame retardant in epoxy resin. The preparation method comprises the following steps: by taking diphenyl hypophosphorous chloride as a basis, preparing a flame-retardant intermediate through nucleophilic substitution reaction between diphenyl hypophosphorous chloride and an aldehyde group-containing phenolic compound, then reacting a phenylboronic acid structure with 3-amino-1, 2-propylene glycol to obtain an amino group-containing phenylboronic acid compound, and finally reacting the phenylboronic acid compound with 3-amino-1, 2-propylene glycol to obtain the amino group-containing phenylboronic acid compound. And finally, carrying out a Schiff base reaction on the flame-retardant intermediate and an amino-containing phenylboronic acid compound to obtain the halogen-free flame retardant containing phosphorus, nitrogen and boron elements. The flame retardant provided by the invention can significantly improve the flame retardant property and mechanical property of epoxy resin. A flame-retardant epoxy resin prepared based on the flame retardant; the influence on Tg of an epoxy resin cured product is small, the smoke suppression and char formation performance and the mechanical performance of the cured product can be remarkably improved, and meanwhile, the flame retardant has excellent flame retardant efficiency; the limit oxygen index of the flame-retardant epoxy resin can reach 31%; the vertical combustion grade is V-0 or above, and the carbon residue amount can reach 18% or above.

The invention relates to the technical field of automobile tires, and discloses a new energy automobile tire self-repairing sealing material adhered with mute cotton. The preparation method comprises the following steps: adding a modified polyurethane adhesive, C5 petroleum resin and a modified carbon nanotube filler into absolute ethyl alcohol, mixing to obtain a self-repairing liquid, adhering polyurethane cotton to the upper part of the self-repairing liquid, and drying to obtain the new energy automobile tire self-repairing sealing material adhered with the mute cotton. Disulfide bonds, boric acid ester bonds and imine bonds introduced into polyurethane through a chain extension reaction and diselenide bonds introduced into carbon nanotubes all belong to dynamic covalent bonds, so that the self-repairing performance of the material is improved; by introducing a rigid benzene ring and naphthyl aromatic structure, the mechanical property of the self-repairing sealing material is improved; the carbon nano tube can play a role in skeleton supporting in a polyurethane matrix, and the mechanical property of the material is further improved by introducing an adamantane rigid structure into the carbon nano tube.

The invention discloses a heavy metal chelating agent for industrial wastewater and a preparation method of the heavy metal chelating agent, and belongs to the technical field of sewage treatment.The preparation method comprises the steps that 2-hydroxyphenylboronic acid is subjected to graft modification through acrylic acid and polymerized on the surface of activated biomass porous carbon powder with acrylic acid, boron-containing polymer modified porous carbon is obtained, and then ferric chloride hexahydrate serves as an iron source; a boron-containing polymer modified porous carbon surface and aminated magnetic adsorption nanospheres are obtained, B-N coordination is formed between the aminated magnetic adsorption nanospheres and the boron-containing polymer modified porous carbon surface, boron element fixation is achieved through modified copolymerization, loss caused by long-time use of the boron element is avoided, lasting and stable chelation is guaranteed, activated biomass porous carbon serves as a carrier, and macromolecular resin serves as a coating layer. The environment-friendly biochar has the advantages of favorable degradability, greenness, degradability, safety and high efficiency, and avoids the problem of secondary pollution caused by the use of a chelating agent.

The invention relates to the technical field of cables, in particular to a high-toughness halogen-free flame-retardant crosslinked cable and a preparation method thereof.High-density polyethylene, ethylene-vinyl acetate copolymer, modified MXene and auxiliaries are mixed and co-extruded, and ultraviolet radiation crosslinking is adopted to prepare a reinforcing layer of the cable; the preparation method comprises the following steps: firstly, coating MXene with dopamine, treating with tert-butyldimethylsilyl chloride, then grafting DOPO (9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide), and then introducing double bonds on the composite MXene; a self-repairing polyurethane emulsion, modified MXene and a photoinitiator are blended to prepare a protective coating, the surface of the reinforcing layer is coated with the protective coating, light curing treatment is carried out, and the water-resistant and corrosion-resistant protective layer sleeve with the self-repairing surface is prepared; a chain extender containing boric acid ester bonds and disulfide bonds is added in the preparation of the self-repairing polyurethane emulsion, and pentaerythritol triacrylate is used as a photosensitizer.

The invention belongs to the field of ceramic material production, and relates to a high-thermal-conductivity silicon carbide ceramic material and a preparation method thereof. The preparation method comprises the following steps: mixing silicon carbide powder, cane sugar, boric acid, a dispersing agent and water to prepare slurry; on the basis that the total mass of the silicon carbide powder, the carbon element obtained after cane sugar is debonded, the boron element in the boric acid and the dispersing agent is 100 wt.%, the adding amount of the carbon element obtained after cane sugar is debonded is 1.0 wt.%-2.5 wt.%, and the adding amount of the boron element in the boric acid is 0.1 wt.%-0.3 wt.%; drying, sieving, forming and debonding the slurry to obtain a ceramic body; and sintering the ceramic green body at normal pressure to obtain the high-thermal-conductivity silicon carbide ceramic material. The water-soluble sucrose and boric acid are added as sintering aids to be mixed with the silicon carbide powder, so that the uniform dispersity of the sintering aids is improved, and finally, the use amount of the sintering aids is effectively reduced while the sintering densification of the ceramic is ensured, thereby reducing the adverse effect of a second phase and internal impurities on the thermal conductivity of the silicon carbide ceramic as much as possible.

The invention discloses a corrosion-resistant polypropylene edge band material and a preparation method thereof, and belongs to the technical field of preparation of edge band materials. The corrosion-resistant polypropylene edge sealing strip material is prepared from, by weight, 50-75 parts of polypropylene, 2-5 parts of an antioxidant, 3-6 parts of a corrosion-resistant agent, 2-4 parts of a composite flame retardant, 8-15 parts of calcium carbonate and 2-4 parts of dye, the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline, and the corrosion-resistant agent is prepared from 2, 6-dichlorobenzonitrile, 1, 2, 4-triazole, a sulfuric acid solution, sodium nitrite and parachloroaniline. The composite flame retardant is prepared from 3-glycidyl ether oxypropyl trimethoxy silane, diphenyl silanediol, barium hydroxide and boric acid. The edge band material prepared by the method has excellent corrosion resistance, flame retardance, heat resistance and mechanical properties.

The invention relates to the technical field of cables, and particularly discloses a high-performance halogen-free flame-retardant flexible power cable. The high-performance halogen-free flame-retardant flexible power cable comprises a core layer, an insulating layer, a flame-retardant layer, a shielding layer and a protective layer which are arranged in sequence, the flame-retardant layer is prepared from the following raw material components in parts by weight: 30 to 40 parts of ethylene-vinyl acetate copolymer, 10 to 20 parts of polyolefin elastomer, 8 to 10 parts of microencapsulated ammonium polyphosphate, 2.5 to 4.5 parts of pentaerythritol, 20 to 30 parts of inorganic flame retardant, 5 to 8 parts of expansible graphite, 2 to 3 parts of diatomite, 0.5 to 1.5 parts of nano kaolin, 2 to 3 parts of zinc borate, 0.1 to 0.5 part of antioxidant and 0.5 to 1.0 part of lubricant. The cable provided by the invention not only has good flame retardant property, but also has certain flexibility.

The invention relates to the technical field of high polymer materials, and provides an anti-aging cable and a preparation method thereof. The anti-aging cable comprises a conductor and a sheath layer, the sheath layer is prepared from the following raw materials in parts by weight: 40 to 60 parts of ethylene propylene diene monomer, 20 to 30 parts of ethylene-vinyl acetate copolymer, 20 to 22 parts of nano cellulose / montmorillonite composite material, 5 to 10 parts of nano silicon dioxide, 10 to 20 parts of magnesium hydroxide, 5 to 8 parts of zinc borate, 1.5 to 3 parts of composite antioxidant, 0.5 to 1.5 parts of ultraviolet light absorber, 1 to 1.2 parts of anti-aging agent and 1 to 2 parts of silane coupling agent. And 0.3 to 0.5 part of maleic anhydride grafted polypropylene. According to the anti-aging cable prepared in the invention, the high temperature resistance and the acid corrosion resistance of the anti-aging cable are improved, and the aging of the cable is effectively delayed.

The invention discloses a coating type high-molecular flame-retardant material. The composite material is prepared from the following components: organic silicon modified epoxy resin, a bio-based castor oil derivative, hydroxyapatite, carbon nanofibers, expanded graphite, ammonium polyphosphate, zinc borate, nano silicon dioxide, molybdenum oxide, microencapsulated red phosphorus, magnesium hydroxide, melamine cyanurate, aluminum diethylphosphinate, pentaerythritol, trihydroxymethyl phosphine oxide and a silane coupling agent. The coating is prepared from a titanate coupling agent, stearic acid, polyethylene glycol, 2, 6-butylated hydroxytoluene, triphenyl phosphite, 2, 4-dihydroxybenzophenone, sebacic diester, polytetrafluoroethylene micro powder, a modified polydimethylsiloxane flatting agent, organic montmorillonite, a polyether modified silicon defoaming agent and a solvent. The invention has the beneficial effects of high flame retardant efficiency, environmental friendliness, excellent comprehensive performance and excellent processability.

The invention discloses a high-strength silicon carbide ceramic material and a preparation method thereof, and relates to the technical field of ceramic material preparation. The silicon carbide ceramic material is prepared from the following raw materials in parts by weight: 70-85 parts of silicon carbide powder, 5-15 parts of B4Cw-coated BN, 3-5 parts of a sintering aid, 0.5-1 part of a dispersing agent and 0.5-2 parts of carbon black, the B4Cw-coated BN is prepared by the following steps: pretreating a boron carbide whisker with a silane coupling agent, adding the pretreated boron carbide whisker into a precursor solution containing boric acid and urea, and reacting to obtain the boron carbide whisker with a BN coating; the sintering aid is formed by mixing Y2O3 and Al2O3; the dispersing agent is ammonium polyacrylate. The preparation method of the high-strength silicon carbide ceramic material comprises the following steps: pretreating boron carbide whiskers, synthesizing B4Cw-coated BN, preparing composite powder, and preparing the silicon carbide ceramic material. The high-strength silicon carbide ceramic material disclosed by the invention has relatively high bending strength and elasticity modulus.

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 a quick-curing polyurethane seamless expansion joint material for roads and a preparation method, and belongs to the technical field of road engineering materials. The material is prepared from polyether polyol, polycaprolactone glycol, a bisphenol A epoxy-polyether block isocyanate terminated prepolymer, a methyl phenyl silicon-boron hybrid hydroxyl chain extender, diphenylmethane diisocyanate, calcium carbonate, wollastonite, a hindered amine anti-aging agent and dioctyl phthalate. Wherein the bisphenol A epoxy-polyether block isocyanate terminated prepolymer is prepared by the following steps: reacting bisphenol A with epoxy chloropropane to generate epoxy resin, reacting with polytetramethylene ether glycol, and introducing isophorone diisocyanate; the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation and ethylene glycol reaction on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester; and the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester. The material has the advantages of quick curing property, weather resistance and high-temperature stability, and is suitable for road seamless expansion joint scenes.

The invention relates to the technical field of packaging materials, in particular to a chip inductor packaging material and a preparation method thereof. The packaging material is prepared from epoxy resin serving as a matrix, composite boron nitride modified hollow glass beads, spherical silica powder, a silane coupling agent, a curing agent, an accelerant and a defoaming agent. Wherein the boron nitride modified hollow glass beads are obtained by constructing a boron nitride functional layer through branched polyamidoamine grafting and a melamine-boric acid in-situ method and carrying out high-temperature calcination. By means of the innovative structural design, efficient bonding of a filler interface and ordered construction of a heat conduction path are achieved, the heat conduction performance and the mechanical strength of the composite material are remarkably improved, and the dielectric constant and the dielectric loss are effectively reduced. The packaging material provided by the invention has excellent electrical, thermal and mechanical comprehensive performance, meets the requirements of light weight and high reliability packaging of a new generation of high-performance chip inductor devices, and has important industrialization and application prospects.

This invention discloses a visible-light-responsive dynamically covalently cross-linked self-healing polyurethane and its preparation method, belonging to the field of self-healing materials technology. The material is prepared by reacting diisocyanate, long-chain diol, butanediol, trimethylolpropane, and a monool containing an azophenylboronic acid structure in a certain proportion at 60°C. This invention achieves visible-light-responsive self-healing of the polyurethane material by introducing a visible-light-responsive azophenylboronic acid structure into the polyurethane and utilizing the photoresponsive cis-trans isomerization of the azo structure to regulate the reversible breakage and recombination of the boron-oxygen hexacyclic ring. The visible-light-responsive dynamically covalently cross-linked self-healing polyurethane material prepared by this invention maintains high mechanical strength (16.47 MPa) while exhibiting a strength self-healing efficiency of 95.8% after 8 hours of visible light irradiation, showing broad application prospects in smart materials, anti-corrosion coatings, and other fields.

The invention relates to the technical field of ceramics, and discloses a high-toughness high-temperature-resistant ceramic material and a preparation method thereof.The high-toughness high-temperature-resistant ceramic material comprises, by weight, 100 parts of quartz powder, 15-32 parts of potassium feldspar, 3-6 parts of boric acid, 0.8-2 parts of modified polysiloxane and the like. And the side chain of the modified polysiloxane contains a large amount of carboxyl, and forms interfacial interaction with the surfaces of the quartz and the potassium feldspar, so that the effect of a dispersing agent is achieved, and the mechanical strength of the calcined ceramic material is favorably improved. Modified polysiloxane contains a naphthalene ring structure with high carbon content, after high-temperature calcination, polysiloxane is taken as a silicon source, naphthalene rings are carbonized, high-temperature pyrolysis is carried out, a large number of silicon carbide reinforced phases are more easily formed, the silicon carbide reinforced phases are uniformly dispersed in a quartz ceramic matrix, the mechanical strength and toughness of the ceramic material are remarkably improved, the high-temperature resistance is excellent, and the modified polysiloxane has good application prospects in heat-resistant ceramic lampshades, heat-resistant ceramic lampshades, heat-resistant ceramic lampshades and heat-resistant ceramic lampshades. The heat-resistant ceramic base has good practical application.

The invention discloses a low-temperature-resistant organic silicon elastic damping body and a preparation method thereof, and belongs to the field of synthesis of organic polymer materials. The invention relates to a high-efficiency photoinitiator, which is prepared from the following ingredients in parts by weight: 95 to 110 parts of fluorosiloxane-phenylsiloxane segmented copolymers, 25 to 35 parts of boric acid ester end-capped polyurethane prepolymers, 10 to 15 parts of neodymium-containing metal organic frameworks, 20 to 40 parts of azobenzene modified CNT / TiO2, 2 to 4 parts of photoinitiators 1173 and 2 to 3 parts of neodymium acetylacetonate. Ultralow-temperature adaptability, self-repairing and high-modulus coexistence and wide-temperature-range damping stability are achieved through fluorosilicone / phenyl block copolymer molecular design, a borate-neodymium coordination double-dynamic network, stress response filler and a light-heat gradient curing process. The low-temperature-resistant organic silicon elastic damping body prepared by the invention provides a new solution idea for an extreme environment damping material, and has a wide application prospect.

The invention relates to the technical field of scale and corrosion inhibitors, in particular to a preparation method and application of an enhanced boric acid efficient environment-friendly phosphorus-free scale and corrosion inhibitor, and the enhanced boric acid efficient environment-friendly phosphorus-free scale and corrosion inhibitor comprises the following components in parts by weight: 50-100 parts of a water-soluble polyol-boric acid mixture, 0-50 parts of polyepoxysuccinic acid, 0-50 parts of polyaspartic acid, 0-50 parts of benzotriazole and 0-50 parts of zinc chloride. The high intermiscibility of polyhydric alcohol, water and boric acid is utilized, the dosage of boric acid in a solution is effectively increased, the effects of boric acid on scale inhibition, corrosion inhibition, sterilization and the like are amplified, meanwhile, the freezing temperature of the scale and corrosion inhibitor is reduced due to the addition of polyhydric alcohol, the scale and corrosion inhibitor can be used in winter more easily, and the scale and corrosion inhibitor is suitable for popularization and application. The invention provides an implementation way of a novel efficient environment-friendly phosphorus-free scale and corrosion inhibitor, and the scale and corrosion inhibitor has the advantages of environment friendliness, convenience in use and good scale and corrosion inhibition performance.

The invention relates to the technical field of metal material hot working, and discloses a hot-rolled coiled plate production process which comprises the following steps: preparing a reaction type protective agent, the high-temperature-resistant coating is prepared from the following raw materials in parts by weight: 20 to 40 parts of tetraethoxysilane, 5 to 15 parts of triethyl phosphate, 1 to 5 parts of triethyl borate, 0.5 to 2.0 parts of cerous nitrate (III) hexahydrate, 0.1 to 1.0 part of lithium acetate and 0.01 to 0.05 part of vanadyl acetylacetonate (IV). Coating the surface of a hot-rolled plate blank with the protective agent; the coated plate blank is heated in a heating furnace, so that the protective agent forms a molten-state protective layer in situ; carrying out hot rolling on the plate blank with the molten protective layer; and cooling and coiling the hot-rolled steel strip. In the whole heating and hot rolling process, the molten protective layer isolates the contact between the steel and the oxidizing atmosphere, so that the generation of oxide scales is fundamentally inhibited, the production process is simplified, and the metal yield is increased.

The invention relates to the technical field of cables, and provides a flame-retardant medium-voltage power cable and a preparation method thereof. The flame-retardant medium-voltage power cable comprises a conductor and a flame-retardant layer, the flame-retardant layer is prepared from the following raw materials in parts by weight: 65 to 75 parts of ethylene-vinyl acetate copolymer, 25 to 35 parts of polyolefin elastomer, 10 to 12 parts of maleic anhydride grafted polyethylene, 10 to 14 parts of phosphorus-nitrogen modified wollastonite, 8 to 10 parts of polydopamine / silane double-layer modified magnesium hydroxide, 3 to 5 parts of nano zinc borate, 0.6 to 1 part of antioxidant and 0.5 to 0.7 part of calcium stearate. According to the flame-retardant medium-voltage power cable prepared in the invention, the flame-retardant performance is improved, and the flame-retardant stability of the cable is also improved.

The invention discloses a recoverable benzoxazine / fiber composite material and a preparation method thereof, and belongs to the technical field of composite materials. The composite material is obtained by hot-pressing and curing degradable benzoxazine containing boric acid ester and fibers according to the mass ratio of 1: (0.1-0.8), the degradable benzoxazine containing the boric acid ester is obtained by reacting diphenol containing a boric acid ester structure, long-chain monoamine and paraformaldehyde according to a molar ratio of 1: 2: (4.1-4.4). The composite material prepared by the invention is obtained by hot-pressing and curing the degradable benzoxazine containing boric acid ester and the fiber, and the reversible boric acid ester bond endows the benzoxazine with excellent degradability and endows the composite material with excellent recoverability, so that the fiber can be reused. In addition, the composite material contains boron element, so that the composite material has excellent flame retardant property. The prepared composite material has wide application prospects in the fields of buildings, traffic, military industry and the like.

The invention relates to a long-term stable carbon dioxide absorbent and a preparation method and application thereof, preparation raw materials of the carbon dioxide absorbent comprise a quaternary ammonium salt hydrogen bond acceptor, an amine compound, an alcohol hydrogen bond donor and a reinforcing agent, and the reinforcing agent comprises sorbitol, boric acid or nano silicon dioxide. The carbon dioxide absorbent disclosed by the invention not only has excellent absorption and desorption effects, but also is creatively added with the reinforcing agent. By adding the reinforcing agent, the long-term operation stability of the absorbent under an oxygen-containing condition can be remarkably improved on the premise that the original excellent CO2 absorption and desorption performance is not influenced basically, and oxidative degradation of amine components is effectively inhibited. The composition is simple to prepare and controllable in cost, and is suitable for efficiently and stably capturing CO2 from gas mixtures such as industrial flue gas.

The invention discloses high magnetic induction oriented silicon steel and a production method. The high magnetic induction oriented silicon steel comprises the following components in percentage by weight: 0.032 to 0.065 percent of C, 2.58 to 4.02 percent of Si, 0.014 to 0.036 percent of Als, 0.021 to 0.043 percent of Mn, 0.0015 to 0.014 percent of Nb, 0.0015 to 0.0084 percent of B, 0.0037 to 0.0081 percent of N and 0.004 to 0.015 percent of S. A large amount of B element is added, a proper amount of BN and other congenital inhibitors can be provided, the situation that primary grains are too large is effectively avoided, meanwhile, boron oxide, boric acid and borate are added into the magnesium oxide additive, an acquired inhibitor can be generated with N, an AlN + BN double-inhibitor system is formed, and the stability of magnetic performance is guaranteed; and the temperature is kept at 910-1005 DEG C for 18-25 hours, so that B is fully diffused and forms a new BN inhibitor with N, and the stability of the magnetic performance is effectively improved.

The invention discloses a preparation method of a road base mixture curing agent based on construction waste recycled aggregate, and relates to the technical field of modified composite materials. According to the method, the construction waste recycled aggregate is collected and treated, and crushing and grinding are performed after impurities are removed, so that a proper particle size is obtained. Then, mixing the modified epoxy resin, a silane coupling agent, nano silicate, an organic silicon water repellent, a surfactant, a defoaming agent and water according to a preset proportion to form a silicate solution; in the preparation process of the modified epoxy resin, an epoxy resin emulsion reacts with other additives in a nitrogen atmosphere, so that the generated curing agent is ensured to have excellent mechanical properties and water resistance. The final curing agent is formed by adding boric acid into a silicate solution, heating and reacting, and drying. The curing agent not only improves the strength and stability of the road base mixture, but also effectively utilizes the construction waste, realizes resource recycling, and meets the requirements of sustainable development.

This invention relates to a method of reducing abnormal combustion events in a hydrogen fueled internal combustion engine (HICE) during operation of the engine. The method includes the steps of: a) providing to the HICE a lubricating oil composition including or resulting from the admixing of: i) a base oil having a KV100 of less than or equal to 12 cSt and included at greater than 40 wt.% of the composition and comprising a Group I base oil, a Group II base oil, or combinations thereof; ii) at least one optionally borated polyisobutylene succinimide (PIBSA-PAM) dispersant at from 0.25 wt.% to 12.0 wt.% of the composition, wherein the optionally borated PIBSA-PAM dispersant is selected from the group consisting of lower molecular weight PIB SA-PAM dispersant (Mn less than 1600 g / mol), higher molecular weight PIBSA-PAM dispersant (Mn 1600 g / mol or more), and combinations thereof; iii) at least one overbased metal containing detergent with a Total Base Number (KOH / g) greater than or equal to 9 and less than or equal to 500 and included at a treat level to deliver between 100 to 5000 ppm by weight of total metal and between 0.15 wt. % to 8.0 wt. % of total soap to the composition; and iv) the lubricating oil composition having a total sulfated ash of less than or equal to 2.5 wt.%, a total phosphorous level of less than or equal to 0.120 wt.%, and a SAE viscosity grade of 25W-X, 20W-X, 15W-X, 10W-X, 5W-X or 0W-X, where X represents any one of 8, 12, 16, 20, 30, 40, 50 or 60; and b) providing a fuel comprising hydrogen to the hydrogen fueled internal combustion engine; and c) combusting the fuel in the hydrogen fueled internal combustion engine. Also provided are lubricating oil compositions for use in a HICE to reduce the propensity for abnormal combustion events.

The invention relates to the technical field of pipes, and discloses an environment-friendly high-strength corrosion-resistant PE pipe production process which comprises the following steps: raw material pretreatment: mixing high-density polyethylene, low-density polyethylene, borate, polyvinylidene fluoride, epoxidized soybean oil and an antioxidant in proportion, and performing melting pretreatment to form a uniform mixture; dynamic cross-linking extrusion molding: carrying out dynamic cross-linking extrusion on the pretreated mixture in a three-zone temperature control extruder, wherein three zones are respectively a dynamic bond activation zone, a chain orientation induction zone and a dynamic locking zone; and carrying out on-line molecular chain orientation stretching: heating the extruded semi-cured pipe, and carrying out one-way or two-way stretching under a constant-temperature condition. Through a dynamic boron-oxygen cross-linked network extrusion process, an on-line molecular chain orientation stretching technology, a partitioned cooling process and a synergistic effect of a polyvinylidene fluoride thin layer coated on the surface, high strength, toughness and balanced inner and outer layer performance of the pipe are effectively realized.

The invention relates to the technical field of sodium ion battery positive electrode materials, in particular to a boric acid modified ternary layered oxide positive electrode material and a preparation method and application thereof. The chemical general formula of the boric acid modified ternary layered oxide positive electrode material is Na2 / 3Ni1 / 3Co1 / 3Mn1 / 3BxO, and x is more than 0 and less than or equal to 0.09; the boric acid modified ternary layered oxide positive electrode material is subjected to boric acid modification treatment and comprises interstitial doping of boron elements and a surface BO coating layer, the interstitial doped boron elements are located at tetrahedral sites of a transition metal layer, and the thickness of the BO coating layer is 3 nm to 10 nm. The boric acid modified ternary layered oxide positive electrode material prepared by the invention shows high specific capacity, good cycling stability and excellent rate capability in the sodium ion battery, and meanwhile, the preparation method disclosed by the invention has the advantages of simple preparation process, high cost effectiveness and the like, and has a wide application prospect.

The invention belongs to the technical field of adhesives, and particularly relates to a degradable mobile phone gum material and a preparation process thereof. The degradable mobile phone gum material is prepared from the following raw materials in parts by weight: 45 to 60 parts of bio-based methacrylate monomer, 5 to 10 parts of tackifying resin, 3 to 8 parts of vinyl ethoxyethyl acrylate, 3 to 8 parts of 4-hydroxybutyl acrylate, 2 to 5 parts of modified monomer A, 2 to 5 parts of modified monomer B, 0.1 to 2 parts of initiator and 60 to 80 parts of solvent, the modified monomer A contains a disulfide bond and a double bond; the modified monomer B contains a boric acid ester bond and a double bond. Dynamic disulfide bonds and boric acid ester bonds are introduced between polyacrylate molecular chains, the two dynamic bonds form a graded energy dissipation network, and the obtained degradable mobile phone back adhesive material is degradable and has an excellent creep recovery rate at the same time.

The invention discloses a preparation method of a rubber waterstop material with a low compression set rate, which comprises the following steps: firstly, carrying out blending reaction on hydroxyl silicone oil and boric acid to obtain liquid polyborosiloxane; the preparation method comprises the following steps: adding liquid polyborosiloxane and natural rubber into an internal mixer according to a ratio, and carrying out internal mixing to obtain a mixture; adding zinc oxide, an anti-aging agent, stearic acid and an anti-tearing agent into the obtained mixture, and continuously mixing; continuously adding kaolin talcum powder, calcium carbonate, calcium oxide, white carbon black, N550, N330 and KH550, and internally mixing again to obtain a preform; adding a vulcanization accelerator and a vulcanizing agent into the preform, and continuously mixing to obtain a rubber material to be vulcanized; and vulcanizing and forming the rubber material to be vulcanized to prepare the rubber water-stop belt material with the low compression set rate. According to the invention, the compression set rate of the rubber material can be reduced while the tensile strength, elongation, tear resistance and other properties of the rubber are not sacrificed, so that the product performance is enhanced.

The invention discloses a catalyst for an n-butene isomerization reaction and a preparation method thereof, and belongs to the technical field of catalysts. The preparation method comprises the following steps: mixing a silicon source, an aluminum source, tetrapropylammonium hydroxide and water, adding boric acid, and crystallizing to obtain a seed crystal; the method comprises the following steps: mixing a silicon source, an aluminum source, pyridine and water, adding a seed crystal and ammonium fluoride, and crystallizing to obtain a core-shell type molecular sieve; adding the core-shell type molecular sieve into the bimetallic complex solution for dipping to obtain a metal-loaded type molecular sieve; adding the metal-loaded molecular sieve into a triethyl phosphine ethanol solution for treatment to obtain a phosphorus-modified molecular sieve; uniformly mixing the phosphorus-modified molecular sieve, pseudo-boehmite, sesbania powder and water, kneading, performing extrusion molding, drying and calcining to obtain the catalyst. The catalyst prepared by the invention is used for n-butene isomerization reaction, and has excellent catalytic activity and isobutene selectivity.